Dysferlin Polyclonal Antibody
Sizes: 50µl, 100µl
Catalogue Numbers: BS90436-50, BS90436-100
Product: Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Swiss-Prot: O75923(Human)
Host: Rabbit
Reactivity: Human
Applications: WB, IHC FC
All Applications: WB:1:500-1:2,000
IHC:1:50-1:200
FC:1:50-1:100
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.
Purification and Purity: Protein affinity purified
Storage and Stability: Store at +4°C after thawing. Aliquot store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Specificity: Dysferlin polyclonal antibody detects endogenous levels of Dysferlin protein.
Bioworld Molecular Weight: 237 kDa
Note: For research use only, not for use in diagnostic procedure.
Extra Notes: Western blot analysis of Dysferlin on human fetal skeletal muscle tissue lysate using anti-Dysferlin antibody at 1/500 dilution., Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-Dysferlin antibody. Counter stained with hematoxylin.
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,
Immunogen: Recombinant protein
Conjugate: Unconjugated
Modification: Unmodified