PMS1 (Human) Recombinant Protein (P01)

Catalog # H00005378-P01

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Size:25 ug
Price: USD $ 510.00
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Size:10 ug
Price: USD $ 335.00
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  • Specification

    Product Description

    Human PMS1 full-length ORF ( AAH08410, 1 a.a. - 166 a.a.) recombinant protein with GST-tag at N-terminal.Full-Length Protein,Full-Length Proteins,Full-Length,Full Length,FullLength

    Sequence

    MKQLPAATVRLLSSSQIITSVVSVVKELIENSLDAGATSVDVKLENYGFDKIEVRDNGEGIKAVDAPVMAMKYYTSKINSHEDLENLTTYGFRGEALGSICCIAEVLITTRTAADNFSTQYVLDGSGHILSQKPSHLGQGKKVALYTNILYLFCLNCWFKKKKVTR

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    44

    Interspecies Antigen Sequence

    Mouse (85); Rat (84)

    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.
    In NCBI database, the accession number (AAH08410) of this protein had been removed, and indicated as obsolete version. However, this product is still available in our catalog for specific research purpose.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

    Western Blot (Recombinant protein)

    Antibody Production

    Protein Array

  • Gene Info — PMS1

    Entrez GeneID

    5378

    GeneBank Accession#

    BC008410

    Protein Accession#

    AAH08410

    Gene Name

    PMS1

    Gene Alias

    DKFZp781M0253, FLJ98259, HNPCC3, PMSL1, hPMS1

    Gene Description

    PMS1 postmeiotic segregation increased 1 (S. cerevisiae)

    Omim ID

    600258

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a protein belonging to the DNA mismatch repair mutL/hexB family. This protein is thought to be involved in the repair of DNA mismatches, and it can form heterodimers with MLH1, a known DNA mismatch repair protein. Mutations in this gene cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype, which is also known as Lynch syndrome. [provided by RefSeq

    Other Designations

    human homolog of yeast mutL|mismatch repair gene PMSL1|postmeiotic segregation 1|rhabdomyosarcoma antigen MU-RMS-40.10B|rhabdomyosarcoma antigen MU-RMS-40.10E

  • 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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