WDR4 antibody

Product Graph
Contáctenos para saber el precio

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
WDR4 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab09493
tested applications
ELISA, WB

Description

Required for the formation of N(7)-methylguanine at position 46(m7G46) in tRNA. In the complex, it is required to stabilize and induce conformational changes of the catalytic subunit.

Documents del producto

Instrucciones
Descargar
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
WD repeat domain 4 (WDR4)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1:200-1:2000
Clonality
polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
30 kDa,20 kDa
Purity
≥95% as determined by SDS-PAGE
Purification
Immunogen affinity purified
Size 1
100µg
Form
liquid
Tested Applications
ELISA, WB
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
UniProt ID
P57081
Gene ID
10785
Alias
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4,Protein Wuho homolog (hWH),WD repeat-containing protein 4,WDR4
Background
Antibody anti-WDR4
Status
RUO
Note
Mol. Weight 30 kDa, 20 kDa

Descripción

Related Products

EH13640

Human WDR4 (WD repeat-containing protein 4) ELISA Kit

Ver Producto
FNab09493

WDR4 antibody

Required for the formation of N(7)-methylguanine at position 46(m7G46) in tRNA. In the complex, it is required to stabilize and induce conformational changes of the catalytic subunit.

Ver Producto
abx029615

WD Repeat-Containing Protein 4 (WDR4) Antibody

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.

Ver Producto