SGCD anticorps (AA 57-289)

N° du produit ABIN5541232

Cet anticorps anti-SGCD est un anticorps Souris Monoclonal détectant SGCD dans WB et EIA. Adapté pour Humain.

Aperçu rapide pour SGCD anticorps (AA 57-289) (ABIN5541232)

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

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp SGCD est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Clone: AT19G8

Détail du produit anti-SGCD anticorps

Épitope: AA 57-289

Purification: Protein-A affinity chromatography

Immunogène: Recombinant human SGCD (57-289aa) purified from E. coli

Information d'application

Indications d'application: The antibody has been tested by ELISA, Western blot analysis to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results. Recommended Starting Dilutions : 1/1000.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS, pH 7.4 containing 0.02 % Sodium Azide and 10 % Glycerol

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store undiluted at 2-8°C for up to two weeks or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. Shelf life: one year from despatch.

Date de péremption: 12 months

Détails sur SGCD

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

Autre désignation: delta-sarcoglycan

Sujet: 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. It is expressed most abundantly in skeletal and cardiac muscle. Mutations in this gene have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding distinct isoforms have been observed for this gene.

UniProt: Q92629

Pathways: Maintenance of Protein Location