SGCD anticorps

N° du produit ABIN7256868

Détail du produit anti-SGCD anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SGCD est non-conjugé

Application: Immunofluorescence (IF)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human SGCD (NP_000328.2).

Isotype: IgG

Information d'application

Indications d'application: IF 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur SGCD

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

Autre désignation: SGCD (SGCD Produits)

Synonymes: anticorps BEST:GH21860, anticorps CG14808, anticorps CT34621, anticorps DmSCG-gammadelta, anticorps Dmel\\CG14808, anticorps EG:4F1.1, anticorps GH21860, anticorps Sgcd, anticorps wu:fc49e11, anticorps zgc:110649, anticorps 35DAG, anticorps CMD1L, anticorps DAGD, anticorps SG-delta, anticorps SGCDP, anticorps SGD, anticorps Delta-SG, anticorps 35kDa, anticorps delta-SG, anticorps sarcoglycan delta, anticorps Sarcoglycan delta, anticorps sarcoglycan, delta (dystrophin-associated glycoprotein), anticorps sarcoglycan, delta, anticorps SGCD, anticorps Scgdelta, anticorps sgcd, anticorps Sgcd

Sujet: The protein encoded by this gene 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 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.

ID gène: 6444

UniProt: Q92629

Pathways: Maintenance of Protein Location