TRAPPC2 (Human) Recombinant Protein (P01)

Catalog # H00006399-P01

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Size:25 ug
Price: USD $ 510.00
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Price: USD $ 335.00
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  • Specification

    Product Description

    Human TRAPPC2 full-length ORF ( AAH16915, 1 a.a. - 140 a.a.) recombinant protein with GST-tag at N-terminal.Full-Length Protein,Full-Length Proteins,Full-Length,Full Length,FullLength

    Sequence

    MSGSFYFVIVGHHDNPVFEMEFLPAGKAESKDDHRHLNQFIAHAALDLVDENMWLSNNMYLKTVDKFNEWFVSAFVTAGHMRFIMLHDIRQEDGIKNFFTDVYDLYIKFSMNPFYEPNSPIRSSAFDRKVQFLGKKHLLS

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    41.14

    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 — TRAPPC2

    Entrez GeneID

    6399

    GeneBank Accession#

    BC016915

    Protein Accession#

    AAH16915

    Gene Name

    TRAPPC2

    Gene Alias

    MIP-2A, SEDL, SEDT, TRS20, ZNF547L, hYP38334

    Gene Description

    trafficking protein particle complex 2

    Omim ID

    300202 313400

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is thought to be part of a large multisubunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind MBP1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT). A processed pseudogene of this gene is located on chromosome 19, and other pseuodogenes are found on chromosomes 8 and Y. Alternatively spliced transcript variants encoding distinct isoforms or having different 5' UTRs, have been found for this gene. [provided by RefSeq

    Other Designations

    MBP-1 interacting protein-2A|sedlin|spondyloepiphyseal dysplasia, late

  • Interactome
  • Publication Reference
    • Interaction of sedlin with pam14.

      Liu X, Wang Y, Zhu H, Zhang Q, Xing X, Wu B, Song L, Fan L.

      Journal of Cellular Biochemistry 2010 Apr; 109(6):1129.

      Application:WB-Ce, Human, HEK 293T, HeLa cells.

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