Application
Fig3: Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue using anti-alpha sarcoglycan antibody. Counter stained with hematoxylin.Application
Fig3: Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue using anti-alpha sarcoglycan antibody. Counter stained with hematoxylin.Application
Fig3: Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue using anti-alpha sarcoglycan antibody. Counter stained with hematoxylin.| Product Name | alpha sarcoglycan [JA51-81] |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | 50 DAG antibody 50 kDa dystrophin associated glycoprotein antibody 50 kDa dystrophin-associated glycoprotein antibody 50DAG antibody 50kD DAG antibody 59kDa antibody A2 antibody adhalin antibody ADL antibody Alpha SG antibody Alpha-sarcoglycan antibody Alpha-SG antibody Asg antibody DAG2 antibody DMDA2 antibody Dystroglycan 2 antibody Dystroglycan-2 antibody LGMD2D antibody sarcoglycan, alpha (dystrophin-associated glycoprotein) antibody SCARMD1 antibody Sgca antibody SGCA_HUMAN antibody |
| Product description | 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. |
| Immunogen | recombinant protein |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgG |
| Host Species | Recombinant rabbit |
| Tested Applications | WBIPIHC |
| WB:1:500-1:2,000 IP:1:50-1:100 IHC:1:50-1:200 |
|
| Species Reactivity | HumanMouseRat |
| Concentration | 1mg/ml |
| Alternative Names | 50 DAG antibody
50 kDa dystrophin associated glycoprotein antibody
50 kDa dystrophin-associated glycoprotein antibody
50DAG antibody
50kD DAG antibody
59kDa antibody
A2 antibody
adhalin antibody
ADL antibody
Alpha SG antibody
Alpha-sarcoglycan antibody
Alpha-SG antibody
Asg antibody
DAG2 antibody
DMDA2 antibody
Dystroglycan 2 antibody
Dystroglycan-2 antibody
LGMD2D antibody
sarcoglycan alpha (dystrophin-associated glycoprotein) antibody SCARMD1 antibody Sgca antibody SGCA_HUMAN antibody |
|---|---|
| Molecular Weight(MW) | 50 kDa |
| Cellular Localization | Cell membrane. Cytoplasm. |
Application
Fig3: Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue using anti-alpha sarcoglycan antibody. Counter stained with hematoxylin.
Application
Fig3: Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue using anti-alpha sarcoglycan antibody. Counter stained with hematoxylin.
Application
Fig3: Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue using anti-alpha sarcoglycan antibody. Counter stained with hematoxylin.| Positive Control | Rat heart cells lysates, mouse heart tissue, mouse skeletal muscle tissue. |
|---|---|
| Application Notes | WB:1:500-1:2,000 IP:1:50-1:100 IHC:1:50-1:200 |
| Form | Liquid |
|---|---|
| Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
| Storage Buffer | 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide. |
