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Anti-gamma Sarcoglycan Antibody (3H334) is a Rabbit antibody targeting gamma Sarcoglycan. Anti-gamma Sarcoglycan Antibody (3H334) can be used in IHC,IP,WB.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
50 μL | $296 | 7-10 days | |
100 μL | $497 | 7-10 days |
Description | Anti-gamma Sarcoglycan Antibody (3H334) is a Rabbit antibody targeting gamma Sarcoglycan. Anti-gamma Sarcoglycan Antibody (3H334) can be used in IHC,IP,WB. |
Synonyms | γSarcoglycan, γ Sarcoglycan, TYPE, SGCG_HUMAN, SGCG, SCG3, SCARMD2, Sarcoglycan gamma, MGC130048, MAM, LGMD2C, gSarcoglycan, Gamma-SG, Gamma-sarcoglycan, gammaSarcoglycan, Gamma SG, g Sarcoglycan, DMDA1, DMDA, DAGA4, A4, 35kDa dystrophin-associated glycoprotein, 35kD dystrophin associated glycoprotein, 35DAG, 35 kDa dystrophin-associated glycoprotein, 35 kDa dystrophin associated glycoprotein |
Ig Type | IgG |
Clone | 3H334 |
Reactivity | Human,Mouse |
Verified Activity | 1. Western blot analysis of gamma Sarcoglycan on human skeletal muscle cells lysates using anti-gamma Sarcoglycan antibody at 1/500 dilution. 2. Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue using anti-gamma Sarcoglycan antibody. Counter stained with hematoxylin. |
Application | |
Recommended Dose | WB: 1:500-2000; IHC: 1:50-200; IP: 1:50-100 |
Antibody Type | Monoclonal |
Host Species | Rabbit |
Construction | Recombinant Antibody |
Purification | ProA affinity purified |
Appearance | Liquid |
Formulation | 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide. |
Research Background | The sarcoglycan transmembrane proteins are members of the dystrophin complex. Sarcoglycans cluster together to form a complex, which is localized in the cell membrane of skeletal, cardiac and smooth muscle fibers. Four sarcoglycan subunit proteins, designated α-, β-, γ- and δ-sarcoglycan, form a complex on the skeletal muscle cell surface membrane. A genetic defect in any one of these proteins causes the loss or marked decrease of the whole sarcoglycan complex, which is observed in the autosomal recessive muscular dystrophy, sarcoglycanopathy. In smooth muscle, β- and δ-sarcoglycans are associated with ε-sarcoglycan, a glycoprotein homologous to α-sarcoglycan. Additionally, a complete deficiency in δ-sarcoglycan is the cause of the Syrian hamster BIO.14 cardiomyopathy. |
Conjucates | Unconjugated |
Immunogen | Recombinant Protein |
Uniprot ID |
Molecular Weight | Theoretical: 32 kDa. |
Stability & Storage | Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
Transport | Shipping with blue ice. |
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