Mouse DMD(Dystrophin) ELISA Kit
Mouse Dystrophin (DMD) ELISA Kit |
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abx572510-96tests | Abbexa | 96 tests | 801.6 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
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DLR-DMD-Mu-48T | DL Develop | 48T | 609.6 EUR |
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Dystrophin (DMD) in samples from tissue homogenates, cell lysates or other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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DLR-DMD-Mu-96T | DL Develop | 96T | 793.2 EUR |
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Dystrophin (DMD) in samples from tissue homogenates, cell lysates or other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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20-abx153933 | Abbexa |
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Mouse dystrophin(DMD)ELISA Kit |
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GA-E0993MS-48T | GenAsia Biotech | 48T | 403.2 EUR |
Mouse dystrophin(DMD)ELISA Kit |
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GA-E0993MS-96T | GenAsia Biotech | 96T | 640.8 EUR |
Mouse Dystrophin, Dmd ELISA KIT |
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ELI-04963m | Lifescience Market | 96 Tests | 1038 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
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SEB503Mu-10x96wellstestplate | Cloud-Clone | 10x96-wells test plate | 5552.14 EUR |
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Dystrophin (DMD) in Tissue homogenates, cell lysates and other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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SEB503Mu-1x48wellstestplate | Cloud-Clone | 1x48-wells test plate | 562.42 EUR |
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Dystrophin (DMD) in Tissue homogenates, cell lysates and other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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SEB503Mu-1x96wellstestplate | Cloud-Clone | 1x96-wells test plate | 752.02 EUR |
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Dystrophin (DMD) in Tissue homogenates, cell lysates and other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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SEB503Mu-5x96wellstestplate | Cloud-Clone | 5x96-wells test plate | 3024.07 EUR |
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Dystrophin (DMD) in Tissue homogenates, cell lysates and other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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4-SEB503Mu | Cloud-Clone |
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Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Mouse Dystrophin (DMD) in samples from Tissue homogenates, cell lysates and other biological fluids. with no significant corss-reactivity with analogues from other species. |
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Mouse Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Mu-48Tests | Reddot Biotech | 48 Tests | 640.8 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Mu-96Tests | Reddot Biotech | 96 Tests | 890.4 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
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RD-DMD-Mu-48Tests | Reddot Biotech | 48 Tests | 613.2 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
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RD-DMD-Mu-96Tests | Reddot Biotech | 96 Tests | 850.8 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Mu-48T | Reddot Biotech | 48T | 465.47 EUR |
Description: tissue homogenates, cell lysates and other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Mu-96T | Reddot Biotech | 96T | 664.97 EUR |
Description: tissue homogenates, cell lysates and other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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DL-DMD-Mu | DL Develop | 96T | 432 EUR |
Description: tissue homogenates, cell lysates or other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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DLR-DMD-Mu | DL Develop | 96T | 454 EUR |
Description: tissue homogenates, cell lysates or other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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RD-DMD-Mu-48T | Reddot Biotech | 48T | 443.3 EUR |
Description: tissue homogenates, cell lysates and other biological fluids. |
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Mouse Dystrophin (DMD) ELISA Kit |
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RD-DMD-Mu-96T | Reddot Biotech | 96T | 633.3 EUR |
Description: tissue homogenates, cell lysates and other biological fluids. |
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ELISA kit for Mouse DMD (Dystrophin) |
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E-EL-M0426 | Elabscience Biotech | 1 plate of 96 wells | 640.8 EUR |
Description: A sandwich ELISA kit for quantitative measurement of Mouse DMD (Dystrophin) in samples from Serum, Plasma, Cell supernatant |
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ELISA kit for Mouse DMD (Dystrophin) |
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ELK3471 | ELK Biotech | 1 plate of 96 wells | 518.4 EUR |
Description: A sandwich ELISA kit for detection of Dystrophin from Mouse in samples from blood, serum, plasma, cell culture fluid and other biological fluids. |
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DMD ELISA Kit| Mouse Dystrophin ELISA Kit |
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EF013570 | Lifescience Market | 96 Tests | 826.8 EUR |
ELISA kit for Mouse Dystrophin (DMD) |
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KTE71245-48T | Abbkine | 48T | 398.4 EUR |
Description: Quantitative sandwich ELISA for measuring Mouse Dystrophin (DMD) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
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ELISA kit for Mouse Dystrophin (DMD) |
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KTE71245-5platesof96wells | Abbkine | 5 plates of 96 wells | 2538 EUR |
Description: Quantitative sandwich ELISA for measuring Mouse Dystrophin (DMD) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
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ELISA kit for Mouse Dystrophin (DMD) |
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KTE71245-96T | Abbkine | 96T | 646.8 EUR |
Description: Quantitative sandwich ELISA for measuring Mouse Dystrophin (DMD) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
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Rat DMD(Dystrophin) ELISA Kit |
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ER0908 | FN Test | 96T | 628.92 EUR |
Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Rattus;Sensitivity: 0.469 ng/ml |
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Rat Dmd/ Dystrophin ELISA Kit |
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E0300Ra | Sunlong | 1 Kit | 685.2 EUR |
Dog DMD/ Dystrophin ELISA Kit |
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E0031Do | Sunlong | 1 Kit | 860.4 EUR |
Human DMD/ Dystrophin ELISA Kit |
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E0707Hu | Sunlong | 1 Kit | 685.2 EUR |
Human DMD(Dystrophin) ELISA Kit |
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EH1726 | FN Test | 96T | 628.92 EUR |
Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Homo sapiens;Sensitivity: 0.094 ng/ml |
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Mouse Dystrophin (DMD) CLIA Kit |
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abx196919-96tests | Abbexa | 96 tests | 990 EUR |
Mouse Dystrophin (DMD) CLIA Kit |
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20-abx492819 | Abbexa |
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CLIA kit for Mouse DMD (Dystrophin) |
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E-CL-M0267 | Elabscience Biotech | 1 plate of 96 wells | 700.8 EUR |
Description: A sandwich CLIA kit for quantitative measurement of Mouse DMD (Dystrophin) in samples from Serum, Plasma, Cell supernatant |
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Rat Dystrophin (DMD) ELISA Kit |
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abx256876-96tests | Abbexa | 96 tests | 801.6 EUR |
Dog Dystrophin (DMD) ELISA Kit |
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abx355448-96tests | Abbexa | 96 tests | 1111.2 EUR |
Pig Dystrophin (DMD) ELISA Kit |
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abx355075-96tests | Abbexa | 96 tests | 990 EUR |
Dog Dystrophin (DMD) ELISA Kit |
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abx517496-96tests | Abbexa | 96 tests | 1111.2 EUR |
Rat Dystrophin (DMD) ELISA Kit |
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abx517500-96tests | Abbexa | 96 tests | 801.6 EUR |
Rat Dystrophin, Dmd ELISA KIT |
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ELI-04964r | Lifescience Market | 96 Tests | 1063.2 EUR |
DMD ELISA Kit| Rat Dystrophin ELISA Kit |
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EF017690 | Lifescience Market | 96 Tests | 826.8 EUR |
Human Dystrophin (DMD) ELISA Kit |
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20-abx151364 | Abbexa |
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Human Dystrophin (DMD) ELISA Kit |
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abx251028-96tests | Abbexa | 96 tests | 801.6 EUR |
Human Dystrophin (DMD) ELISA Kit |
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abx051660-96tests | Abbexa | 96 tests | 801.6 EUR |
Sheep Dystrophin (DMD) ELISA Kit |
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abx355367-96tests | Abbexa | 96 tests | 1111.2 EUR |
Human Dystrophin (DMD) ELISA Kit |
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abx570218-96tests | Abbexa | 96 tests | 801.6 EUR |
Human Dystrophin (DMD) ELISA Kit |
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DLR-DMD-Hu-48T | DL Develop | 48T | 597.6 EUR |
Description: A sandwich quantitative ELISA assay kit for detection of Human Dystrophin (DMD) in samples from tissue homogenates, cell lysates or other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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DLR-DMD-Hu-96T | DL Develop | 96T | 776.4 EUR |
Description: A sandwich quantitative ELISA assay kit for detection of Human Dystrophin (DMD) in samples from tissue homogenates, cell lysates or other biological fluids. |
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Human Dystrophin(DMD)ELISA Kit |
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GA-E1462HM-48T | GenAsia Biotech | 48T | 346.8 EUR |
Human Dystrophin(DMD)ELISA Kit |
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GA-E1462HM-96T | GenAsia Biotech | 96T | 559.2 EUR |
Human Dystrophin, DMD ELISA KIT |
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ELI-04962h | Lifescience Market | 96 Tests | 988.8 EUR |
Human Dystrophin (DMD) ELISA Kit |
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SEB503Hu-10x96wellstestplate | Cloud-Clone | 10x96-wells test plate | 5402.92 EUR |
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Dystrophin (DMD) in tissue homogenates, cell lysates and other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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SEB503Hu-1x48wellstestplate | Cloud-Clone | 1x48-wells test plate | 550.13 EUR |
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Dystrophin (DMD) in tissue homogenates, cell lysates and other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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SEB503Hu-1x96wellstestplate | Cloud-Clone | 1x96-wells test plate | 734.46 EUR |
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Dystrophin (DMD) in tissue homogenates, cell lysates and other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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SEB503Hu-5x96wellstestplate | Cloud-Clone | 5x96-wells test plate | 2945.08 EUR |
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Dystrophin (DMD) in tissue homogenates, cell lysates and other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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4-SEB503Hu | Cloud-Clone |
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Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Human Dystrophin (DMD) in samples from tissue homogenates, cell lysates and other biological fluids with no significant corss-reactivity with analogues from other species. |
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Human Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Hu-48Tests | Reddot Biotech | 48 Tests | 626.4 EUR |
Human Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Hu-96Tests | Reddot Biotech | 96 Tests | 868.8 EUR |
Human Dystrophin(DMD)ELISA Kit |
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QY-E03009 | Qayee Biotechnology | 96T | 480 EUR |
Human Dystrophin (DMD) ELISA Kit |
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RD-DMD-Hu-48Tests | Reddot Biotech | 48 Tests | 600 EUR |
Human Dystrophin (DMD) ELISA Kit |
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RD-DMD-Hu-96Tests | Reddot Biotech | 96 Tests | 830.4 EUR |
Human Dystrophin(DMD)ELISA Kit |
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YLA0632HU-48T | Shanghai YL Biotech | 48T | 435 EUR |
Human Dystrophin(DMD)ELISA Kit |
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YLA0632HU-96T | Shanghai YL Biotech | 96T | 562.5 EUR |
Human Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Hu-48T | Reddot Biotech | 48T | 453.92 EUR |
Description: tissue homogenates, cell lysates and other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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RDR-DMD-Hu-96T | Reddot Biotech | 96T | 648.38 EUR |
Description: tissue homogenates, cell lysates and other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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DL-DMD-Hu | DL Develop | 96T | 421 EUR |
Description: tissue homogenates, cell lysates or other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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DLR-DMD-Hu | DL Develop | 96T | 443 EUR |
Description: tissue homogenates, cell lysates or other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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RD-DMD-Hu-48T | Reddot Biotech | 48T | 432.3 EUR |
Description: tissue homogenates, cell lysates and other biological fluids. |
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Human Dystrophin (DMD) ELISA Kit |
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RD-DMD-Hu-96T | Reddot Biotech | 96T | 617.5 EUR |
Description: tissue homogenates, cell lysates and other biological fluids. |
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ELISA kit for Rat DMD (Dystrophin) |
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E-EL-R0346 | Elabscience Biotech | 1 plate of 96 wells | 640.8 EUR |
Description: A sandwich ELISA kit for quantitative measurement of Rat DMD (Dystrophin) in samples from Serum, Plasma, Cell supernatant |
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Rabbit Dystrophin (DMD) ELISA Kit |
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abx355333-96tests | Abbexa | 96 tests | 990 EUR |
Monkey Dystrophin (DMD) ELISA Kit |
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abx354916-96tests | Abbexa | 96 tests | 990 EUR |
Canine Dystrophin, DMD ELISA KIT |
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ELI-04965d | Lifescience Market | 96 Tests | 1113.6 EUR |
ELISA kit for Human DMD (Dystrophin) |
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E-EL-H1436 | Elabscience Biotech | 1 plate of 96 wells | 640.8 EUR |
Description: A sandwich ELISA kit for quantitative measurement of Human DMD (Dystrophin) in samples from Serum, Plasma, Cell supernatant |
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ELISA kit for Human DMD (Dystrophin) |
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ELK2055 | ELK Biotech | 1 plate of 96 wells | 518.4 EUR |
Description: A sandwich ELISA kit for detection of Dystrophin from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids. |
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Chicken Dystrophin (DMD) ELISA Kit |
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abx354772-96tests | Abbexa | 96 tests | 990 EUR |
Porcine Dystrophin, DMD ELISA KIT |
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ELI-04960p | Lifescience Market | 96 Tests | 1113.6 EUR |
Chicken Dystrophin, DMD ELISA KIT |
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ELI-04961c | Lifescience Market | 96 Tests | 1113.6 EUR |
Mouse Dystrophin (DMD) Protein |
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20-abx066370 | Abbexa |
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ELISA kit for Human Dystrophin (DMD) |
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KTE62014-48T | Abbkine | 48T | 424.8 EUR |
Description: Quantitative sandwich ELISA for measuring Human Dystrophin (DMD) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
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ELISA kit for Human Dystrophin (DMD) |
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KTE62014-5platesof96wells | Abbkine | 5 plates of 96 wells | 2702.4 EUR |
Description: Quantitative sandwich ELISA for measuring Human Dystrophin (DMD) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
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ELISA kit for Human Dystrophin (DMD) |
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KTE62014-96T | Abbkine | 96T | 686.4 EUR |
Description: Quantitative sandwich ELISA for measuring Human Dystrophin (DMD) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
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Guinea pig Dystrophin (DMD) ELISA Kit |
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abx354829-96tests | Abbexa | 96 tests | 990 EUR |
Dystrophin (DMD) Antibody |
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abx232423-100ug | Abbexa | 100 ug | 577.2 EUR |
Dystrophin (DMD) Antibody |
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20-abx100315 | Abbexa |
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Dystrophin (DMD) Antibody |
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20-abx100316 | Abbexa |
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Dystrophin (DMD) Antibody |
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20-abx176215 | Abbexa |
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Dystrophin (DMD) Antibody |
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20-abx172180 | Abbexa |
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Dystrophin (DMD) Antibody |
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20-abx211560 | Abbexa |
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Dystrophin (DMD) Antibody |
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20-abx149852 | Abbexa |
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Dystrophin (DMD) Antibody |
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20-abx112214 | Abbexa |
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Dystrophin (DMD) Antibody |
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20-abx001224 | Abbexa |
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Dystrophin Antibody / DMD |
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V8862-100UG | NSJ Bioreagents | 100ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V8862-20UG | NSJ Bioreagents | 20ug | 153.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V8862SAF-100UG | NSJ Bioreagents | 100ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V4009-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V4009-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V4009SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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RQ5369 | NSJ Bioreagents | 100 ul | 356.15 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
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Dystrophin Antibody / DMD |
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V7540-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V7540-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V7540IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V7540SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V7547-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V7547-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V7547IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V7547SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
|||
V7548-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
|||
V7548-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7548IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7548SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
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Dystrophin Antibody / DMD |
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V7555-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
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Dystrophin Antibody / DMD |
|||
V7555-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
|||
Dystrophin Antibody / DMD |
|||
V7555IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
|||
Dystrophin Antibody / DMD |
|||
V7555SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq] |
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Dystrophin Antibody / DMD |
|||
V7561-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7561-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7561IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7561SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7562-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7562-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7562IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
|||
Dystrophin Antibody / DMD |
|||
V7562SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission. |
Mouse DMD(Dystrophin) ELISA Kit