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Anti-Calpain 3 antibody - Domain I, large subunit
See all Calpain 3 products (13) ...
Rabbit polyclonal to Calpain 3 - Domain I, large subunit
Ab38960 binds to Calpain 3 (reduced and non reduced), and recognizes both the latent and active forms of the protein. It does not cross react with the other Calpain family members (m calpain, M calpain, LP-82/85 Calpain, ncl2, ncl3, etc.). The rat 88 and 90 kD novel Calpains share the insert #1, and ab38960 may crossreact with these forms.
Reacts with
Human
Predicted to work with
Mouse, Rat
Synthetic peptide based on domain I of human Calpain 3 large subunit.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: 0.05% Sodium Azide
Constituents: 50% Glycerol
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Cell Biology >> Proteolysis / Ubiquitin >> Proteolytic enzymes >> Cysteine protease >> Calpains
Signal Transduction >> Signaling Pathway >> Calcium Signaling >> Calpain
Our Abpromise guarantee covers the use of ab38960 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Recommended starting dilution of 1/1000 (when using colorimetric substrates such as BCIP/NBT) and 1/5000 (for chemiluminescent substrates). Higher concentrations of antibody may be needed for samples from more distantly related species. Detects bands of approximately 94, 82, 62 and 60 kDa and a series of further cleaved active forms when used against the reduced protein (predicted molecular weight of the latent form: 94 kDa). Note: EDTA/EGTA treatment of tissues or lysates is required to see latent zymogen. Dilution optimised using Chromogenic detection. Not yet tested in other applications. Optimal dilutions/concentrations should be determined by the end user.
Calcium-regulated non-lysosomal thiol-protease.
Isoform I is skeletal muscle specific.
Defects in CAPN3 are the cause of limb-girdle muscular dystrophy type 2A (LGMD2A) [MIM:253600]. LGMD2A is an autosomal recessive degenerative myopathy characterized by progressive symmetrical atrophy and weakness of the proximal limb muscles and elevated serum creatine kinase. The symptoms usually begin during the first two decades of life, and the disease gradually worsens, often resulting in loss of walking ability 10 or 20 years after onset.
Belongs to the peptidase C2 family.
Contains 1 calpain catalytic domain.
Contains 4 EF-hand domains.
Cytoplasm.
Target information above from: UniProt accessionP20807
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
This product has been referenced in:
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