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Recombinant Human Protein cereblon (CRBN)

ACP00412

Number
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Specifications


Cat.No ACP00412 Target NameCRBN
FormLiquid or Lyophilized powderExpression SystemMammalian cell
Expression Range1-442aaMol Weight53.0 kDa
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 IDQ96SW2
Background Information
  • Uniprot Id

    Q96SW2

  • Target Species

    Human

  • Target Name

    CRBN

  • Target Full Name

    Protein cereblon

  • Target Function

    Substrate recognition component of a DCX (DDB1-CUL4-X-box) E3 protein ligase complex that mediates the ubiquitination and subsequent proteasomal degradation of target proteins, such as MEIS2 (Probable). Normal degradation of key regulatory proteins is required for normal limb outgrowth and expression of the fibroblast growth factor FGF8. Maintains presynaptic glutamate release and consequently cognitive functions, such as memory and learning, by negatively regulating large-conductance calcium-activated potassium (BK) channels in excitatory neurons. Likely to function by regulating the assembly and neuronal surface expression of BK channels via its interaction with KCNT1. May also be involved in regulating anxiety-like behaviors via a BK channel-independent mechanism.

  • Target Involvement

    Mental retardation, autosomal recessive 2A (MRT2A)

  • Target Subcellular Location

    Cytoplasm. Nucleus. Membrane; Peripheral membrane protein.

  • Target Protein Families

    CRBN family

  • Target Tissue Specificity

    Widely expressed. Highly expressed in brain.

  • Target Research Area

    Neuroscience

  • Target Synonyms

    CRBN; AD-006; Protein cereblon

  • Target Background

    This gene encodes a protein related to the Lon protease protein family. In rodents and other mammals this gene product is found in the cytoplasm localized with a calcium channel membrane protein, and is thought to play a role in brain development. Mutations in this gene are associated with autosomal recessive nonsyndromic cognitive disability. Multiple transcript variants encoding different isoforms have been found for this gene.

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