概述

产品描述	Rabbit Polyclonal antibody recognizes GNB1L
反应物种	Hu, Ms, Rat
应用	WB
宿主	Rabbit
克隆	Polyclonal
同位型	IgG
靶点名称	GNB1L
抗原物种	Human
抗原	Recombinant protein of Human GNB1L
偶联标记	Un-conjugated
別名	G protein subunit beta-like protein 1; WD repeat-containing protein 14; WDR14; Guanine nucleotide-binding protein subunit beta-like protein 1; DGCRK3; WD40 repeat-containing protein deleted in VCFS; GY2; WDVCF; FKSG1

应用说明

应用建议	应用 推荐稀释比 WB 1:500 - 1:2000
应用说明	* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
阳性对照	Mouse heart

属性

形式	Liquid
纯化	Affinity purification with immunogen.
缓冲液	PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
抗菌剂	0.02% sodium azide
稳定剂	50% Glycerol
存放说明	For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项	For laboratory research only, not for drug, diagnostic or other use.

生物信息

数据库连接	GeneID: 13972 Mouse GNB1L GeneID: 54584 Human GNB1L Swiss-port # Q9BYB4 Human Guanine nucleotide-binding protein subunit beta-like protein 1 Swiss-port # Q9EQ15 Mouse Guanine nucleotide-binding protein subunit beta-like protein 1
基因名称	GNB1L
全名	guanine nucleotide binding protein (G protein), beta polypeptide 1-like
背景介绍	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. [provided by RefSeq, Jul 2008]
预测分子量	36 kDa

检测图片 (1) Click the Picture to Zoom In