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Recombinant Human Prolactin regulatory element-binding protein (PREB), Truncated

ACP01906

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Specifications


Cat.No ACP01906 Target NamePREB
Target SynonymsMammalian guanine nucleotide exchange factor mSec12FormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range1-388aa
Mol Weight49.8 kDaProtein LengthPartial
PurityGreater than 85% 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 IDQ9HCU5
Background Information
  • Uniprot Id

    Q9HCU5

  • Target Species

    Human

  • Target Name

    PREB

  • Target Full Name

    Guanine nucleotide-exchange factor SEC12

  • Target Function

    Guanine nucleotide exchange factor that specifically activates the small GTPase SAR1B. Mediates the recruitment of SAR1B and other COPII coat components to endoplasmic reticulum membranes and is therefore required for the formation of COPII transport vesicles from the ER.; Was first identified based on its probable role in the regulation of pituitary gene transcription. Binds to the prolactin gene (PRL) promoter and seems to activate transcription.

  • Target Subcellular Location

    Endoplasmic reticulum membrane; Single-pass membrane protein. Nucleus.

  • Target Tissue Specificity

    Ubiquitous.

  • Target Research Area

    Epigenetics and Nuclear Signaling

  • Target Synonyms

    Mammalian guanine nucleotide exchange factor mSec12; Preb; PREB_HUMAN; Prolactin regulatory binding element protein; Prolactin regulatory element binding; Prolactin regulatory element binding protein; Prolactin regulatory element-binding protein; SEC12

  • Target Background

    This gene encodes a protein that specifically binds to a Pit1-binding element of the prolactin (PRL) promoter. This protein may act as a transcriptional regulator and is thought to be involved in some of the developmental abnormalities observed in patients with partial trisomy 2p. This gene overlaps the abhydrolase domain containing 1 (ABHD1) gene on the opposite strand.

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