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Dystrophin Antibody

Catalog Number:

49412
other_names: BMD antibody
CMD3B antibody
DMD antibody
DMD_HUMAN antibody
Duchenne muscular dystrophy protein antibody
Dystrophin antibody
Muscular dystrophy Duchenne and Becker types antibody

Amount:

100μg
calculated_mw: 427 kDa
host_species: Rabbit

Price:

$319

Swiss-Prot No:

Swiss-Prot#:P11532

Form of Antibody:

1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.

Storage/Stability:

Immunogen:

recombinant protein

Purification:

ProA affinity purified

Specificity/Sensitivity:

Applications:

WB, IHC

Background:

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 eight independent tissue-specific promoters and two 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.

References:

appl_detail:

WB: 1:1,000
IHC: 1:50-1:200


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