本公司产品仅供体外研究使用,不用于临床诊断

GNB1L Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-17869

宿主: Rabbit

反应性: H,M

应用: IHC

  • 详情
  • Overview

    Synonyms DGCRK3,ESTM55 ,fb98e06,fj09d12,FKSG1,G protein subunit beta-like protein 1,G-protein beta subunit-like protein,GNB1L,GNB1L,guanine nucleotide binding protein (G protein), beta polypeptide 1-like,guanine nucleotide binding protein beta-subunit-like polypeptide,Guanine nucleotide-binding protein subunit beta-like protein 1,GY2,KIAA1645,WD repeat-containing protein 14,WD40 repeat-containing protein deleted in VCFS,WDR14,WDVCF,wu:fb98e06,wu:fj09d12 ,zgc:55774,GNB1L抗体
    Swissprot Q9BYB4
    Source Rabbit
    Reactivity Human, Mouse
    Immunogen Synthetic peptide of human GNB1L
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:30-1:150
    Concentration 1mg/mL
    Clonality Polyclonal

    Properties

    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
    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.
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