SGCD antibody

Catalog No. ABIN7231336

This anti-SGCD antibody is a Rabbit Polyclonal antibody detecting SGCD in WB and ELISA. Suitable for Human and Mouse.

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: SGCD Polyclonal Antibody

Specificity: The antibody detects endogenous levels of SGCD protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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 (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: 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.

Target Details for SGCD

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

Alternative Name: SGCD

Background: Rabbit Anti-SGCD Polyclonal Antibody,35 kDa dystrophin-associated glycoprotein, 35DAG,The 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.,SGCD

Molecular Weight: observerd band 31kDa

Gene ID: 6444

UniProt: Q92629

Pathways: Maintenance of Protein Location