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WDR4 Recombinant Rabbit Monoclonal Antibody [JE58-28] (ET7111-37)

Price: Regular price $385.00

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Catalog# ET7111-37

Rabbit Monoclonal to WDR4

Tested for

  • WB

  • IHC-P

  • FC

Reacts with

  • Human

Recombinant production enables lot-to-lot consistency and is animal-cruelty-free

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Specifications

Product Type

Recombinant Rabbit monoclonal primary

Product Name

WDR4 Recombinant Rabbit Monoclonal Antibody [JE58-28] (ET7111-37)

Immunogen

Recombinant protein within human wdr4 aa 262-412.

Host

Rabbit

Positive Control

K562 cell lysates, human liver carcinoma tissue, human cervical carcinoma tissue, human ovarian tumor tissue, Daudi.

Conjugation

Unconjugated

Clonality

Monoclonal

Clone Number

JE58-28

RRID

AB_3071094

APPLICATION DILUTION

  • WB

  • 1:500-1:1,000

  • IHC-P

  • 1:50-1:200

  • FC

  • 1:50-1:100

PROPERTIES

Form

Liquid

Storage Condition

Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.

Storage Buffer

1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.

Concentration

1ug/ul

Purification

Protein A affinity purified.

Molecular Weight

45 kDa

Isotype

IgG

TARGET

UNIPROT #

P57081

PROTEIN NAME

WDR4

SYNONYMS

"OTTHUMP00000109401 antibody;OTTHUMP00000109402 antibody;TRM82 antibody;tRNA (guanine N(7) ) methyltransferase subunit WDR4 antibody;tRNA (guanine-N(7)-)-methyltransferase subunit WDR4 antibody;WD repeat containing protein 4 antibody;WD repeat protein 4 antibody;WD repeat protein domain 4 protein isoform 2 antibody;WD repeat-containing protein 4 antibody;wdr4 antibody;WDR4_HUMAN antibody"

SUBCELLULAR LOCATION

Nucleus, Chromosome.

FUNCTION

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. Alternatively spliced transcript variants have been found for this gene.

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