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Recombinant Human Smad nuclear-interacting protein 1 (SNIP1)

ACP13630

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP13630 Target NameSNIP1
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Expression Range1-396Protein LengthFull length protein
Purity>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 IDQ8TAD8
Background Information
  • Uniprot Id

    Q8TAD8

  • Target Species

    Human

  • Target Name

    SNIP1

  • Target Full Name

    Smad nuclear-interacting protein 1

  • Target Function

    Required for pre-mRNA splicing as component of the spliceosome. Down-regulates NF-kappa-B signaling by competing with RELA for CREBBP/EP300 binding. Involved in the microRNA (miRNA) biogenesis. May be involved in cyclin-D1/CCND1 mRNA stability through the SNARP complex which associates with both the 3'end of the CCND1 gene and its mRNA.

  • Target Involvement

    Psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED)

  • Target Subcellular Location

    Nucleus.

  • Target Tissue Specificity

    Ubiquitous, with highest expression in heart and skeletal muscle.

  • Target Synonyms

    FHA domain containing protein SNIP1; FHA domain-containing protein SNIP1; FLJ12553; PMRED; Smad nuclear interacting protein (Smad nuclear interacting); smad nuclear interacting protein 1; Smad nuclear interacting protein; Smad nuclear-interacting protein 1; SNIP1 (Smad nuclear interacting protein); SNIP1; SNIP1_HUMAN; Splicing factor arginine/serine rich 4 (Pre mRNA splicing factor SRP75)

  • Target Background

    This gene encodes a protein that contains a coiled-coil motif and C-terminal forkhead-associated (FHA) domain. The encoded protein functions as a transcriptional coactivator that increases c-Myc activity and inhibits transforming growth factor beta (TGF-beta) and nuclear factor kappa-B (NF-kB) signaling. The encoded protein also regulates the stability of cyclin D1 mRNA, and may play a role in cell proliferation and cancer progression. Mutations in this gene are a cause of psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED).

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