GAPT anticorps (AA 21-120)

N° du produit ABIN1713503

L’anticorps Lapin Polyclonal anti-GAPT a été validé pour WB, ELISA, ICC, IF (cc), IF (p), IHC (fro) et IHC (p). Il convient pour détecter GAPT dans des échantillons de Humain.

Aperçu rapide pour GAPT anticorps (AA 21-120) (ABIN1713503)

Antigène: GAPT (GRB2-Binding Adaptor Protein, Transmembrane (GAPT))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GAPT est non-conjugé

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

Détail du produit anti-GAPT anticorps

Épitope: AA 21-120

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human GAPT

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 GAPT

Antigène: GAPT (GRB2-Binding Adaptor Protein, Transmembrane (GAPT))

Autre désignation: GAPT

Sujet:

Synonyms: C5orf29, Gapt, GAPT_HUMAN, Grb2-binding adaptor transmembrane, Growth factor receptor-bound protein 2-binding adapter protein, Growth factor receptor-bound protein 2-binding adapter protein, transmembrane, Protein GAPT, transmembrane.

Background: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf29 gene product has been provisionally designated C5orf29 pending further characterization.

ID gène: 202309