SGCA anticorps (AA 60-290)

N° du produit ABIN1682687

Détail du produit anti-SGCA anticorps

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

Épitope: AA 60-290

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SGCA est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Séquence: ITYHAHLQGH PDLPRWLRYT QRSPHHPGFL YGSATPEDRG LQVIEVTAYN RDSFDTTRQR LVLEIGDPEG PLLPYQAEFL VRSHDAEEVL PSTPASRFLS ALGGLWEPGE LQLLNVTSAL DRGGRVPLPI EGRKEGVYIK VGSASPFSTC LKMVASPDSH ARCAQGQPPL LSCYDTLAPH FRVDWCNVTL VDKSVPEPAD EVPTPGDGIL EHDPFFCPPT EAPDRDFLVD A

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 60-290 of human alpha Sarcoglycan (alpha Sarcoglycan (SGCA)) (NP_000014.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IF,1:50 - 1:200

Restrictions: For Research Use only

Stockage

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 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.,SGCA,50DAG,ADL,DAG2,DMDA2,LGMD2D,SCARMD1,adhalin,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,SGCA

Poids moléculaire: 29 kDa/42 kDa

ID gène: 6442

UniProt: Q16586