SNTG2 anticorps (AA 181-280)

N° du produit ABIN1385151

Détail du produit anti-SNTG2 anticorps

Antigène: SNTG2 (Syntrophin, gamma 2 (SNTG2))

Épitope: AA 181-280

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SNTG2 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

Homologie: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SNTG2

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur SNTG2

Antigène: SNTG2 (Syntrophin, gamma 2 (SNTG2))

Autre désignation: SNTG2/Syntrophin 5 (SNTG2 Produits)

Synonymes: anticorps MGC84699, anticorps SNTG2, anticorps G2SYN, anticorps SYN5, anticorps 2210008K22Rik, anticorps 9530013L23, anticorps BB121248, anticorps syntrophin, gamma 2 L homeolog, anticorps syntrophin gamma 2, anticorps syntrophin, gamma 2, anticorps sntg2.L, anticorps SNTG2, anticorps Sntg2

Sujet:

Synonyms: G2SYN, Gamma2-syntrophin, SNTG2, SYN5, Syntrophin-5, Syntrophin5, Syntrophin 5, Syntrophin gamma 2, SNTG2_HUMAN.

Background: Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy.