Vergleich

WDR4 Antibody (monoclonal) (M01)

ArtNr ABC-AT4531a
Hersteller Abcepta
Menge 100 ug
Kategorie
Typ Antibody Primary
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
Applikationen WB, IHC, ELISA
Clon 1F9
Specific against other
Host Mouse
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Similar products tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4 {ECO:0000255|HAMAP-Rule:MF_03056}, WD repeat-containing protein 4 {ECO:0000255|HAMAP-Rule:MF_03056}, WDR4 {ECO:0000255|HAMAP-Rule:MF_03056}
Lieferbar
Primary Accession
P57081
Antigen Type
Recombinant Protein
Application
WB, IHC, E
Bio Background
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.
Bio References
Toward a confocal subcellular atlas of the human proteome. Barbe L, et al. Mol Cell Proteomics, 2008 Mar. PMID 18029348.Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. Olsen JV, et al. Cell, 2006 Nov 3. PMID 17081983.Cell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteins. Hu YH, et al. BMC Genomics, 2006 Jun 16. PMID 16780588.Towards a proteome-scale map of the human protein-protein interaction network. Rual JF, et al. Nature, 2005 Oct 20. PMID 16189514.The tRNA methylase METTL1 is phosphorylated and inactivated by PKB and RSK in vitro and in cells. Cartlidge RA, et al. EMBO J, 2005 May 4. PMID 15861136.
Clonality
Monoclonal
Gene ID
10785
Gene Name
WDR4 {ECO:0000255|HAMAP-Rule:MF_03056, ECO:0000312|HGNC:HGNC:12756}
Subtitle
Mouse monoclonal antibody raised against a full length recombinant WDR4.
Reactivity
H
Legend image 1
Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (55 KDa) .
Type image 1
WB
Dilution image 1
1:500~1000
Legend image 2
WDR4 monoclonal antibody (M01), clone 1F9 Western Blot analysis of WDR4 expression in Hela S3 NE ( (Cat # AT4531a )
Type image 2
WB
Dilution image 2
1:500~1000
Legend image 3
Western Blot analysis of WDR4 expression in transfected 293T cell line by WDR4 monoclonal antibody (M01), clone 1F9.

Lane 1: WDR4 transfected lysate (Predicted MW: 45.5 KDa).
Lane 2: Non-transfected lysate.
Type image 3
WB
Dilution image 3
1:500~1000
Legend image 4
Immunoperoxidase of monoclonal antibody to WDR4 on formalin-fixed paraffin-embedded human small Intestine. [antibody concentration 1 ug/ml]
Type image 4
IHC
Legend image 5
Detection limit for recombinant GST tagged WDR4 is approximately 1ng/ml as a capture antibody.
Type image 5
E
Other Accession
BC001074
Isotype
IgG1 Kappa
Antigen Source
Human: ~~ Positive
Target/Specificity
WDR4 (AAH01074, 1 a.a. ~ 266 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
NCBI Accession
NP_001247403.1; NP_001247404.1; NP_001247405.1; NP_001247406.1; NP_061139.2; NP_387510.1
Clone: 1F9
Org Accession
AAH01074
Gene Description
WD repeat domain 4
Gene Summary
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. [provided by RefSeq

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Menge: 100 ug
Lieferbar: In stock
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