Dysferlin polyclonal, anti-human

Background:
Key calcium ion sensor involved in the Ca2+-triggered synaptic vesicle-plasma membrane fusion. Plays a role in the sarcolemma repair mechanism of both skeletal muscle and cardiomyocytes that permits rapid resealing of membranes disrupted by mechanical stress.

Alternative Name:
DYSF, FER1L1, DMAT, DYSF, DYSF, Dysferlin, Dysferlin limb girdle muscular dystrophy 2B (autosomal recessive), Dysferlin limb girdle muscular dystrophy 2B, Dystrophy associated fer 1 like 1, Dystrophy associated fer 1 like protein, Dystrophy associated fer1 like 1, Dystrophy associated fer1 like protein, Dystrophy-associated fer-1-like protein, Fer 1 like protein 1, Fer-1-like protein 1, Fer1 like protein 1, FER1L1, FLJ00175, FLJ90168, LGMD 2B, LGMD2B, Limb girdle muscular dystrophy 2B (autosomal recessive), Limb girdle muscular dystrophy 2B, Miyoshi myopathy, MM, MMD1,

Application Dilution:
WB:1:500-1:2,000
IHC:1:50-1:200
FC:1:50-1:100

Specificity: Dysferlin polyclonal antibody detects endogenous levels of Dysferlin protein.

Immunogen:
Recombinant protein

MW: 237 kDa

Swiss-Prot: O75923(Human)

Purification & Purity:
Protein affinity purified

Format:
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2

Storage:
Store at +4°C after thawing. Aliquot store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

For research use only, not for use in diagnostic procedure.