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Recombinant Human Guanine nucleotide-binding protein subunit beta-like protein 1 (GNB1L)

ACP03206

Number
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Specifications


Cat.No ACP03206 Target NameGNB1L
FormLiquid or Lyophilized powderExpression SystemE.coli
Expression Range1-327aaMol Weight62.6kDa
Protein LengthFull lengthPurityGreater than 90% as determined by SDS-PAGE.
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ9BYB4
Background Information
  • Uniprot Id

    Q9BYB4

  • Target Species

    Human

  • Target Name

    GNB1L

  • Target Full Name

    Guanine nucleotide-binding protein subunit beta-like protein 1

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    DGCRK3; ESTM55 ; fb98e06; fj09d12; FKSG1; G protein subunit beta-like protein 1; G-protein beta subunit-like protein; GNB1L; GNB1L_HUMAN; 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

  • Target 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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