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WB analysis of various sample lysates using GTX66505 GNB1L antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX66505 GNB1L antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX66505 GNB1L antibody. Dilution : 1:1000 Loading : 25microg per lane

GNB1L antibody

GTX66505
GeneTex
ApplicationsWestern Blot
Product group Antibodies
TargetGNB1L
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Overview

  • Supplier
    GeneTex
  • Product Name
    GNB1L antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID54584
  • Target name
    GNB1L
  • Target description
    G protein subunit beta 1 like
  • Target synonyms
    DGCRK3, FKSG1, GY2, WDR14, WDVCF, guanine nucleotide-binding protein subunit beta-like protein 1, G-protein beta subunit-like protein, WD repeat-containing protein 14, WD40 repeat-containing protein deleted in VCFS, g protein subunit beta-like protein 1, guanine nucleotide binding protein (G protein), beta polypeptide 1-like, guanine nucleotide binding protein beta-subunit-like polypeptide
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9BYB4
  • Protein Name
    Guanine nucleotide-binding protein subunit beta-like protein 1
  • Scientific Description
    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]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203