UTRN (Human) Recombinant Protein (Q01)

Catalog # H00007402-Q01

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Size:10 ug
Price: USD $ 335.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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  • Specification

    Product Description

    Human UTRN partial ORF ( NP_009055, 3328 a.a. - 3433 a.a.) recombinant protein with GST-tag at N-terminal.

    Sequence

    LEARMQILEDHNKQLESQLHRLRQLLEQPESDSRINGVSPWASPQHSALSYSLDPDASGPQFHQAAGEDLLAPPHDTSTDLTEVMEQIHSTFPSCCPNVPSRPQAM

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    37.4

    Interspecies Antigen Sequence

    Mouse (92)

    Preparation Method

    in vitro wheat germ expression system

    Purification

    Glutathione Sepharose 4 Fast Flow

    Quality Control Testing

    12.5% SDS-PAGE Stained with Coomassie Blue.

    Storage Buffer

    50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

    Note

    Best use within three months from the date of receipt of this protein.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

    Western Blot (Recombinant protein)

    Antibody Production

    Protein Array

  • Gene Info — UTRN

    Entrez GeneID

    7402

    GeneBank Accession#

    NM_007124

    Protein Accession#

    NP_009055

    Gene Name

    UTRN

    Gene Alias

    DMDL, DRP, DRP1, FLJ23678

    Gene Description

    utrophin

    Omim ID

    128240

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq

    Other Designations

    OTTHUMP00000017350|OTTHUMP00000040139|dystrophin-related protein

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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