Mouse DMD(Dystrophin) ELISA Kit
Mouse Dystrophin (DMD) ELISA Kit |
|||
RDR-DMD-Mu-48Tests | Reddot Biotech | 48 Tests | 640.8 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
|||
RDR-DMD-Mu-96Tests | Reddot Biotech | 96 Tests | 890.4 EUR |
Human Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Human Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Human Dystrophin (DMD) ELISA Kit |
|||
RD-DMD-Hu-48Tests | Reddot Biotech | 48 Tests | 600 EUR |
Human Dystrophin (DMD) ELISA Kit |
|||
RD-DMD-Hu-96Tests | Reddot Biotech | 96 Tests | 830.4 EUR |
Human Dystrophin (DMD) ELISA Kit |
|||
RDR-DMD-Hu-48Tests | Reddot Biotech | 48 Tests | 626.4 EUR |
Human Dystrophin (DMD) ELISA Kit |
|||
RDR-DMD-Hu-96Tests | Reddot Biotech | 96 Tests | 868.8 EUR |
Mouse Dmd/ Dystrophin ELISA Kit |
|||
E0409Mo | Sunlong | 1 Kit | 685.2 EUR |
Mouse DMD(Dystrophin) ELISA Kit |
|||
EM0989 | FN Test | 96T | 628.92 EUR |
Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Mus ;Sensitivity: 0.188 ng/ml |
|||
Mouse Dystrophin (DMD) ELISA Kit |
|||
20-abx153933 | Abbexa |
|
|
Mouse Dystrophin (DMD) ELISA Kit |
|||
abx572510-96tests | Abbexa | 96 tests | 801.6 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
|||
abx255323-96tests | Abbexa | 96 tests | 801.6 EUR |
Mouse Dystrophin, Dmd ELISA KIT |
|||
ELI-04963m | Lifescience Market | 96 Tests | 1038 EUR |
Mouse dystrophin(DMD)ELISA Kit |
|||
GA-E0993MS-48T | GenAsia Biotech | 48T | 403.2 EUR |
Mouse dystrophin(DMD)ELISA Kit |
|||
GA-E0993MS-96T | GenAsia Biotech | 96T | 640.8 EUR |
Mouse Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Mouse Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Mouse Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Mouse Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Mouse Dystrophin (DMD) ELISA Kit |
|||
4-SEB503Mu | Cloud-Clone |
|
|
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. |
|||
Mouse Dystrophin ELISA Kit (DMD) |
|||
RK02753 | Abclonal | 96 Tests | 625.2 EUR |
ELISA kit for Mouse DMD (Dystrophin) |
|||
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 |
|||
ELISA kit for Mouse DMD (Dystrophin) |
|||
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. |
|||
ELISA kit for Mouse Dystrophin (DMD) |
|||
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. |
|||
ELISA kit for Mouse Dystrophin (DMD) |
|||
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. |
|||
ELISA kit for Mouse Dystrophin (DMD) |
|||
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. |
|||
DMD ELISA Kit| Mouse Dystrophin ELISA Kit |
|||
EF013570 | Lifescience Market | 96 Tests | 826.8 EUR |
Mouse Dystrophin (DMD) CLIA Kit |
|||
abx196919-96tests | Abbexa | 96 tests | 990 EUR |
Mouse Dystrophin (DMD) CLIA Kit |
|||
20-abx492819 | Abbexa |
|
|
Mouse Dystrophin (DMD) Protein |
|||
20-abx066370 | Abbexa |
|
|
Dog DMD/ Dystrophin ELISA Kit |
|||
E0031Do | Sunlong | 1 Kit | 860.4 EUR |
Human DMD/ Dystrophin ELISA Kit |
|||
E0707Hu | Sunlong | 1 Kit | 685.2 EUR |
Rat Dmd/ Dystrophin ELISA Kit |
|||
E0300Ra | Sunlong | 1 Kit | 685.2 EUR |
Rat DMD(Dystrophin) ELISA Kit |
|||
ER0908 | FN Test | 96T | 628.92 EUR |
Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Rattus;Sensitivity: 0.469 ng/ml |
|||
Human Dystrophin (DMD) ELISA Kit |
|||
20-abx151364 | Abbexa |
|
|
Human Dystrophin (DMD) ELISA Kit |
|||
abx051660-96tests | Abbexa | 96 tests | 801.6 EUR |
Chicken Dystrophin (DMD) ELISA Kit |
|||
abx354772-96tests | Abbexa | 96 tests | 990 EUR |
Monkey Dystrophin (DMD) ELISA Kit |
|||
abx354916-96tests | Abbexa | 96 tests | 990 EUR |
Pig Dystrophin (DMD) ELISA Kit |
|||
abx355075-96tests | Abbexa | 96 tests | 990 EUR |
Rabbit Dystrophin (DMD) ELISA Kit |
|||
abx355333-96tests | Abbexa | 96 tests | 990 EUR |
Sheep Dystrophin (DMD) ELISA Kit |
|||
abx355367-96tests | Abbexa | 96 tests | 1111.2 EUR |
Dog Dystrophin (DMD) ELISA Kit |
|||
abx355448-96tests | Abbexa | 96 tests | 1111.2 EUR |
Human Dystrophin (DMD) ELISA Kit |
|||
abx570218-96tests | Abbexa | 96 tests | 801.6 EUR |
Dog Dystrophin (DMD) ELISA Kit |
|||
abx517496-96tests | Abbexa | 96 tests | 1111.2 EUR |
Rat Dystrophin (DMD) ELISA Kit |
|||
abx517500-96tests | Abbexa | 96 tests | 801.6 EUR |
Human Dystrophin (DMD) ELISA Kit |
|||
abx251028-96tests | Abbexa | 96 tests | 801.6 EUR |
Rat Dystrophin (DMD) ELISA Kit |
|||
abx256876-96tests | Abbexa | 96 tests | 801.6 EUR |
Human DMD(Dystrophin) ELISA Kit |
|||
EH1726 | FN Test | 96T | 628.92 EUR |
Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Homo sapiens;Sensitivity: 0.094 ng/ml |
|||
Porcine Dystrophin, DMD ELISA KIT |
|||
ELI-04960p | Lifescience Market | 96 Tests | 1113.6 EUR |
Chicken Dystrophin, DMD ELISA KIT |
|||
ELI-04961c | Lifescience Market | 96 Tests | 1113.6 EUR |
Human Dystrophin, DMD ELISA KIT |
|||
ELI-04962h | Lifescience Market | 96 Tests | 988.8 EUR |
Rat Dystrophin, Dmd ELISA KIT |
|||
ELI-04964r | Lifescience Market | 96 Tests | 1063.2 EUR |
Canine Dystrophin, DMD ELISA KIT |
|||
ELI-04965d | Lifescience Market | 96 Tests | 1113.6 EUR |
Human Dystrophin(DMD)ELISA Kit |
|||
GA-E1462HM-48T | GenAsia Biotech | 48T | 346.8 EUR |
Human Dystrophin(DMD)ELISA Kit |
|||
GA-E1462HM-96T | GenAsia Biotech | 96T | 559.2 EUR |
Human Dystrophin(DMD)ELISA Kit |
|||
QY-E03009 | Qayee Biotechnology | 96T | 480 EUR |
Human Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Human Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Human Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Human Dystrophin (DMD) ELISA Kit |
|||
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. |
|||
Human Dystrophin (DMD) ELISA Kit |
|||
4-SEB503Hu | Cloud-Clone |
|
|
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. |
|||
Human Dystrophin(DMD)ELISA Kit |
|||
YLA0632HU-48T | Shanghai YL Biotech | 48T | 435 EUR |
Human Dystrophin(DMD)ELISA Kit |
|||
YLA0632HU-96T | Shanghai YL Biotech | 96T | 562.5 EUR |
Dystrophin (DMD) Antibody |
|||
20-abx100315 | Abbexa |
|
|
Dystrophin (DMD) Antibody |
|||
20-abx100316 | Abbexa |
|
|
Dystrophin (DMD) Antibody |
|||
20-abx172180 | Abbexa |
|
|
Dystrophin (DMD) Antibody |
|||
20-abx149852 | Abbexa |
|
|
Dystrophin (DMD) Antibody |
|||
20-abx112214 | Abbexa |
|
|
Dystrophin (DMD) Antibody |
|||
20-abx001224 | Abbexa |
|
|
Dystrophin (DMD) Antibody |
|||
20-abx211560 | Abbexa |
|
|
Dystrophin (DMD) Antibody |
|||
abx232423-100ug | Abbexa | 100 ug | 577.2 EUR |
Dystrophin (DMD) Antibody |
|||
20-abx176215 | Abbexa |
|
|
Recombinant Dystrophin (DMD) |
|||
4-RPB503Hu01 | Cloud-Clone |
|
|
Description: Recombinant Human Dystrophin expressed in: E.coli |
|||
Recombinant Dystrophin (DMD) |
|||
4-RPB503Mu01 | Cloud-Clone |
|
|
Description: Recombinant Mouse Dystrophin expressed in: E.coli |
|||
Dystrophin Antibody / DMD |
|||
RQ5369 | NSJ Bioreagents | 100 ul | 419 EUR |
Dystrophin Antibody / DMD |
|||
V8443-100UG | NSJ Bioreagents | 100 ug | 499 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 |
|||
V8443-20UG | NSJ Bioreagents | 20 ug | 219 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 |
|||
V8443SAF-100UG | NSJ Bioreagents | 100 ug | 499 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 |
|||
V7540-100UG | NSJ Bioreagents | 100 ug | 499 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 |
|||
V7540-20UG | NSJ Bioreagents | 20 ug | 219 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 |
|||
V7540IHC-7ML | NSJ Bioreagents | 7 ml | 499 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 |
|||
V7540SAF-100UG | NSJ Bioreagents | 100 ug | 499 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 |
|||
V7547-100UG | NSJ Bioreagents | 100 ug | 499 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 |
|||
V7547-20UG | NSJ Bioreagents | 20 ug | 219 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 |
|||
V7547IHC-7ML | NSJ Bioreagents | 7 ml | 499 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 |
|||
V7547SAF-100UG | NSJ Bioreagents | 100 ug | 499 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 |
|||
V7548-100UG | NSJ Bioreagents | 100 ug | 499 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 |
|||
V7548-20UG | NSJ Bioreagents | 20 ug | 219 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 | 499 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 | 499 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 |
|||
V7555-100UG | NSJ Bioreagents | 100 ug | 499 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 |
|||
V7555-20UG | NSJ Bioreagents | 20 ug | 219 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 | 499 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 | 499 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 |
|||
V7561-100UG | NSJ Bioreagents | 100 ug | 499 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 | 219 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 | 499 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 | 499 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 | 499 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 | 219 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 | 499 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 | 499 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 |
|||
V8862-100UG | NSJ Bioreagents | 100ug | 499 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 |
|||
V8862-20UG | NSJ Bioreagents | 20ug | 219 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 |
|||
V8862SAF-100UG | NSJ Bioreagents | 100ug | 499 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 |
|||
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. |
|||
Dystrophin Antibody / DMD |
|||
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. |
|||
Dystrophin Antibody / DMD |
|||
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. |
|||
CLIA kit for Mouse DMD (Dystrophin) |
|||
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 |
|||
ELISA kit for Human DMD (Dystrophin) |
|||
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 |
|||
ELISA kit for Rat DMD (Dystrophin) |
|||
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 |
|||
ELISA kit for Human DMD (Dystrophin) |
|||
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. |
|||
Guinea pig Dystrophin (DMD) ELISA Kit |
|||
abx354829-96tests | Abbexa | 96 tests | 990 EUR |
ELISA kit for Human Dystrophin (DMD) |
|||
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. |
|||
ELISA kit for Human Dystrophin (DMD) |
|||
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. |
|||
ELISA kit for Human Dystrophin (DMD) |
|||
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. |
|||
Dystrophin (DMD) Polyclonal Antibody (Mouse) |
|||
4-PAB503Mu01 | Cloud-Clone |
|
|
Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD) |
|||
DMD ELISA Kit| Rat Dystrophin ELISA Kit |
|||
EF017690 | Lifescience Market | 96 Tests | 826.8 EUR |
Human Dystrophin (DMD) CLIA Kit |
|||
abx196619-96tests | Abbexa | 96 tests | 990 EUR |
Rat Dystrophin (DMD) CLIA Kit |
|||
abx196920-96tests | Abbexa | 96 tests | 990 EUR |
Human Dystrophin (DMD) CLIA Kit |
|||
20-abx492818 | Abbexa |
|
|
Human Dystrophin (DMD) Protein |
|||
20-abx066369 | Abbexa |
|
|
Polyclonal DMD / Dystrophin Antibody |
|||
APR11762G | Leading Biology | 0.05mg | 580.8 EUR |
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human DMD / Dystrophin . This antibody is tested and proven to work in the following applications: |
|||
Anti-Dystrophin/DMD Antibody |
|||
PB9276 | BosterBio | 100ug/vial | 400.8 EUR |
Mouse DMD(Dystrophin) ELISA Kit