WDR4 anticorps

N° du produit ABIN2735512

L’anticorps anti-WDR4 Monoclonal Souris est utilisé pour la détection de WDR4 dans des échantillons de Humain. Il a été validé pour WB, IF et FACS.

Aperçu rapide pour WDR4 anticorps (ABIN2735512)

Antigène: WDR4 (WD Repeat Domain 4 (WDR4))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp WDR4 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone: 4G1

Détail du produit anti-WDR4 anticorps

Attributs du produit: Homo sapiens WD repeat domain 4 (WDR4), transcript variant 2

Purification: Purified from mouse ascites fluids by affinity chromatography

Immunogène: Full length human recombinant protein of human WDR4(NP_387510) produced in HEK293T cell.

Isotype: IgG1

Information d'application

Indications d'application: WB 1:2000, IF 1:100, FLOW 1:100,

Commentaires:

The concentration of the product may vary between diferrent lots.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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: -20 °C

Détails sur WDR4

Antigène: WDR4 (WD Repeat Domain 4 (WDR4))

Autre désignation: WDR4

Sujet: This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Two transcript variants encoding the same protein have been found for this gene.

Poids moléculaire: 45.3 kDa

ID gène: 10785

NCBI Accession: NM_033661

HGNC: 10785