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Last updated: 2017/3/19

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PMS1 (Human) Recombinant Protein (P01)

  • Catalog # : H00005378-P01
  • Visit Frequency :
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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.
  • Sequence:
  • MKQLPAATVRLLSSSQIITSVVSVVKELIENSLDAGATSVDVKLENYGFDKIEVRDNGEGIKAVDAPVMAMKYYTSKINSHEDLENLTTYGFRGEALGSICCIAEVLITTRTAADNFSTQYVLDGSGHILSQKPSHLGQGKKVALYTNILYLFCLNCWFKKKKVTR
  • Host:
  • Wheat Germ (in vitro)
  • Theoretical MW (kDa):
  • 44
  • Purification:
  • Glutathione Sepharose 4 Fast Flow
  • Quality Control Testing:
  • 12.5% SDS-PAGE Stained with Coomassie Blue.

    QC Testing of H00005378-P01
  • 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
  • Application Image
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Gene Information
  • Entrez GeneID:
  • 5378
  • Gene Name:
  • PMS1
  • Gene Alias:
  • DKFZp781M0253,FLJ98259,HNPCC3,PMSL1,hPMS1
  • Gene Description:
  • PMS1 postmeiotic segregation increased 1 (S. cerevisiae)
  • 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
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