Anti-Delta sarcoglycan antibody
Specifications
| Product Cat#: | AB-06-1355 |
| Product type: | Primary antibody |
| Antigen: | Delta sarcoglycan |
| Immunogen: | Recombinant protein |
| Species immunized: | Rabbit |
| Isotype: | IgG |
| Applications: | Western Blot (1:400-1:2000); Immunohistochemistry (1:100-1:200); Immunoprecipitation (1:20-1:50) |
| Reactivity: | Human |
| Clonality (clone number): | Monoclonal (JM61-10) |
| Form: | Liquid |
| Buffer: | 1*TBS (pH 7.4), 1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
| Concentration: | 1 mg/ml |
| Purity: | Protein A affinity purified |
| Storage: | Aliquot and freeze at -20℃. Avoid multiple freeze/thaw cycles. |
| Alternative names: | 35 kDa dystrophin associated glycoprotein antibody |
| 35 kDa dystrophin-associated glycoprotein antibody | |
| 35DAG antibody | |
| CMD1L antibody | |
| DAGD antibody | |
| Delta-sarcoglycan antibody | |
| Delta-SG antibody | |
| Dystrophin associated glycoprotein delta sarcoglycan antibody | |
| LGMD2F antibody | |
| MGC22567 antibody | |
| Placental delta sarcoglycan antibody | |
| Sarcoglycan delta (35 kDa dystrophin associated glycoprotein) antibody | |
| SG delta antibody | |
| SGCD antibody | |
| SGCD_HUMAN antibody | |
| SGCDP antibody | |
| SGD antibody |
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Target information
Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix. Defects in SGCD are the cause of limb-girdle muscular dystrophy type 2F (LGMD2F) [MIM:601287]. LGMD2F is an autosomal recessive disorder. Defects in SGCD are the cause of cardiomyopathy dilated type 1L (CMD1L) [MIM:606685]. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.
Provider
Erpantech Laboratory
