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中文名稱：兔抗GNB1L多克隆抗體

英文名稱： Anti-GNB1L rabbit polyclonal antibody

別名： G protein subunit beta 1 like GY2; FKSG1; WDR14; WDVCF; DGCRK3

相關類別：一抗

儲存： 冷凍（-20℃）

宿主： Rabbit

抗原： GNB1L

反應種屬： Human, Mouse

標記物： Unconjugate

克隆類型： rabbit polyclonal

技術規(guī)格

Background:

This gene encodes a G-protein beta-subunit-like polypeptide which is 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 protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene.

Applications:

ELISA, IHC

Name of antibody:

GNB1L

Immunogen:

Synthetic peptide of human GNB1L

Full name:

G protein subunit beta 1 like

Synonyms:

GY2; FKSG1; WDR14; WDVCF; DGCRK3

SwissProt:

Q9BYB4

ELISA Recommended dilution:

5000-10000

IHC positive control:

Human liver cancer;

IHC Recommend dilution:

25-100

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兔抗GNB1L多克隆抗體說明書
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兔抗GNB1L多克隆抗體

Background:	This gene encodes a G-protein beta-subunit-like polypeptide which is 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 protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene.
Applications:	ELISA, IHC
Name of antibody:	GNB1L
Immunogen:	Synthetic peptide of human GNB1L
Full name:	G protein subunit beta 1 like
Synonyms:	GY2; FKSG1; WDR14; WDVCF; DGCRK3
SwissProt:	Q9BYB4
ELISA Recommended dilution:	5000-10000
IHC positive control:	Human liver cancer;
IHC Recommend dilution:	25-100