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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