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Recombinant Human Ribosome-binding protein 1 (RRBP1), Truncated

ACP11125

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP11125 Target NameRRBP1
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Protein LengthPartialPurity>85% (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 IDQ9P2E9
Background Information
  • Uniprot Id

    Q9P2E9

  • Target Species

    Human

  • Target Name

    RRBP1

  • Target Full Name

    Ribosome-binding protein 1

  • Target Function

    Acts as a ribosome receptor and mediates interaction between the ribosome and the endoplasmic reticulum membrane.

  • Target Subcellular Location

    Endoplasmic reticulum membrane; Single-pass type III membrane protein.

  • Target Synonyms

    180 kDa ribosome receptor homolog; DKFZp586A1420; ES/130; ES/130 related protein; ES/130-related protein; ES130; FLJ36146; hES; KIAA1398; MGC157720; MGC157721; Ribosome binding protein 1; Ribosome binding protein 1 homolog 180kDa; Ribosome binding protein 1 homolog; Ribosome receptor protein; Ribosome-binding protein 1; RRBP 1; Rrbp1; RRBP1_HUMAN; RRP

  • Target Background

    This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12.

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