Dystrophin Antibody, mAb, Rabbit
Dystrophin Antibody, MAb, Rabbit

Western blot analysis of Dystrophin expression in human fetal heart lysate.

Dystrophin Antibody, mAb, Rabbit

Anchors the extracellular matrix to the cytoskeleton via F-actin. Ligand for dystroglycan. Component of the dystrophin-associated glycoprotein complex which accumulates at the neuromuscular junction (NMJ) and at a variety of synapses in the peripheral and central nervous systems and has a structural function in stabilizing the sarcolemma. Also implicated in signaling events and synaptic transmission.
A03496
¥37,309.00

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Overview
Specificity This product is specific to Dystrophin
Host Species Rabbit
Immunogen A synthesized peptide derived from human Dystrophin
Species Reactivity Human; Mouse; Rat
Conjugate Unconjugated

Applications
Working concentrations for specific applications should be determined by the investigators. The appropriate concentrations may be affected by secondary antibody affinity, antigen concentration, the sensitivity of the method of detection, temperature, the length of the incubations, and other factors. The suitability of this antibody for applications other than those listed below has not been determined. The following concentration ranges are recommended starting points for this product.
Application Recommended Usage
Western Blot 1:1000-1:2000

Properties
Form Liquid
Storage Buffer Supplied in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.
Storage Instructions Store at -20°C. This product is stable for 1 year upon receipt, when handled and stored as instructed.
Purification Affinity-chromatography
Isotype Rabbit IgG
Clonality Monoclonal

Examples
  • Dystrophin Antibody, MAb, Rabbit
    • Dystrophin Antibody, MAb, Rabbit

    Western blot analysis of Dystrophin expression in human fetal heart lysate.


Background
Target Background Anchors the extracellular matrix to the cytoskeleton via F-actin. Ligand for dystroglycan. Component of the dystrophin-associated glycoprotein complex which accumulates at the neuromuscular junction (NMJ) and at a variety of synapses in the peripheral and central nervous systems and has a structural function in stabilizing the sarcolemma. Also implicated in signaling events and synaptic transmission.
Synonyms BMD; CMD3B; DMD; Dystrophin;

For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.