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PMS1 Antibody (C-term)

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

  • WB - PMS1 Antibody (C-term) AP14975B
    PMS1 Antibody (C-term) (Cat. #AP14975b) western blot analysis in A549 cell line lysates (35ug/lane).This demonstrates the PMS1 antibody detected the PMS1 protein (arrow).
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession P54277
Other Accession NP_000525.1
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 105830 Da
Antigen Region 694-722 aa
Additional Information
Gene ID 5378
Other Names PMS1 protein homolog 1, DNA mismatch repair protein PMS1, PMS1, PMSL1
Target/Specificity This PMS1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 694-722 amino acids from the C-terminal region of human PMS1.
Dilution WB~~1:1000
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsPMS1 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name PMS1
Synonyms PMSL1
Function Probably involved in the repair of mismatches in DNA.
Cellular Location Nucleus {ECO:0000255|PROSITE- ProRule:PRU00267}
Citations (0)

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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.


Hong, K.W., et al. J. Hum. Genet. 55(6):336-341(2010)
Monsees, G.M., et al. Breast Cancer Res. Treat. (2010) In press :
Guey, L.T., et al. Eur. Urol. 57(2):283-292(2010)
Hosgood, H.D. III, et al. Respir Med 103(12):1866-1870(2009)
Adeyemo, A., et al. PLoS Genet. 5 (7), E1000564 (2009) :

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$ 295.00
$ 99.00
Cat# AP14975B
(40 western blots)
Availability: In Stock
Bulk Size
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