SGCD antibody

Catalog No. ABIN7231336

The Rabbit Polyclonal anti-SGCD antibody (ABIN7231336) specifically detects SGCD in WB and ELISA. The antibody is reactive with Human and Mouse samples.

Quick Overview for SGCD antibody (ABIN7231336)

Target: SGCD (Sarcoglycan, delta (35kDa Dystrophin-Associated Glycoprotein) (SGCD))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SGCD antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-SGCD Antibody

Purpose: Rabbit Anti-SGCD Polyclonal Antibody

Specificity: The antibody detects endogenous levels of SGCD protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human SGCD protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for SGCD

Target: SGCD (Sarcoglycan, delta (35kDa Dystrophin-Associated Glycoprotein) (SGCD))

Alternative Name: SGCD

Background: 35 kDa dystrophin-associated glycoprotein, 35DAGThe protein encoded by SGCD is one of the four known components of the sarcoglycan complex, which is a subcomplex of the dystrophin-glycoprotein complex (DGC). DGC forms a link between the F-actin cytoskeleton and the extracellular matrix. This protein is expressed most abundantly in skeletal and cardiac muscle. Mutations in SGCD have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding distinct isoforms have been observed for SGCD.

Molecular Weight: 31kD

Gene ID: 6444

UniProt: Q92629

Pathways: Maintenance of Protein Location