SGCA anticorps (AA 239-266)

N° du produit ABIN1538155

Détail du produit anti-SGCA anticorps

Antigène: SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))

Épitope: AA 239-266

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SGCA est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This SGCA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 239-266 amino acids from the Central region of human SGCA.

Clone: RB36903

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: SGCA Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur SGCA

Antigène: SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))

Autre désignation: SGCA (SGCA Produits)

Synonymes: anticorps Sgca, anticorps 50-DAG, anticorps A2, anticorps ADL, anticorps DAG2, anticorps DMDA2, anticorps LGMD2D, anticorps SCARMD1, anticorps adhalin, anticorps 50DAG, anticorps Asg, anticorps sarcoglycan alpha, anticorps sarcoglycan, alpha (dystrophin-associated glycoprotein), anticorps sarcoglycan, alpha, anticorps SGCA, anticorps Sgca

Sujet: This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.

Poids moléculaire: 42875

ID gène: 6442

NCBI Accession: NP_000014, NP_001129169

UniProt: Q16586