Dystrophin Antibody
Dystrophin (DMD) gene has 79 exons spanning at least 2,300 kb (2.3 Mb) . The C terminus of the dystrophin protein is encoded by a highly conserved, alternatively spliced region of the gene. beta-dystroglycan binding activity is expressed by the dystrophin fragment spanning amino acids 3026-3345 containing the ZZ domain. DMD transcript is formed by at least 60 exons; the first half of the transcript is formed by a minimum of 33 exons spanning nearly 1000 kb, and the remaining portion has at least 27 exons that may spread over a similar distance. Dystrophin gene is expressed at a higher level in primary cultures of neuronal cells than in astro-glial cells derived from adult mouse brain. overexpression of dystrophin prevents the development of the abnormal mechanical properties associated with dystrophic muscle without causing deleterious side effects.
Product Specifications
Specifications
Western blot: 1-2 µg/mL, IHC (FFPE) : 2-4 µg/mL
Host
Mouse
Reactivity
Human, Mouse, Rat, Rabbit
Immunogen
Recombinant human dystrophin fragment was used as the immunogen for this Dystrophin antibody.
Clonality
Monoclonal
Isotype
IgG2b
Clone
MANDYS8
Applications
WB, IHC-P
Purity
Ascites
Format
Ascites
Buffer
0.5mg/ml with 1% BSA and 0.01% sodium azide if reconstituted with 0.2ml sterile 1XPBS
Reconstitution
Limitations
This Dystrophin antibody is available for research use only.
Storage Conditions
Product Datasheet
https://www.nsjbio.com/tds-pdf/dystrophin-antibody-mandys8-r30032
Formulation
0.5 mg/mL with 1% BSA and 0.01% sodium azide if reconstituted with 0.2ml sterile 1X PBS
Applications Notes
CAS Number
9007-83-4
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