WDR4 anticorps (AA 146-173)

N° du produit ABIN1537867

Détail du produit anti-WDR4 anticorps

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

Épitope: AA 146-173

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WDR4 est non-conjugé

Application: Western Blotting (WB)

Homologie: B, M

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This WDR4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 146-173 amino acids from the Central region of human WDR4.

Clone: RB36209

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: WDR4 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur WDR4

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

Autre désignation: WDR4 (WDR4 Produits)

Synonymes: anticorps TRM82, anticorps TRMT82, anticorps AI415180, anticorps AI448349, anticorps D530049K22Rik, anticorps WD repeat domain 4, anticorps WD repeat domain 4 S homeolog, anticorps WDR4, anticorps Wdr4, anticorps wdr4.S

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: 45490

ID gène: 10785

NCBI Accession: NP_001247403, NP_001247404, NP_001247405, NP_001247406, NP_061139, NP_387510

UniProt: P57081