santa cruz biotechnology, inc.
SCBT Logo

Welcome!        Items in Cart     Quick Order

PMS2 (349.29.5.2) Antibody: sc-56203

 |  Datasheet
  • mouse monoclonal IgG1, 100µg/ml
  • raised against recombinant fragment PMS2 corresponding to the first 133 amino acid residues of human origin
  • recommended for detection of PMS2 of human origin by WB and IP
 
Additional PMS Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IP   siRNA  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human PMS2 5395 7p22.1 NM_000535 P54278
608623
 
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
PMS2 (349.29.5.2) sc-56203 100 µg/ml $279
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
PMS2 siRNA (h) sc-36287 10 µM $258
PMS2 (h)-PR sc-36287-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
PMS2 shRNA Plasmid (h) sc-36287-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
PMS2 shRNA (h) Lentiviral Particles sc-36287-V 200 µl $625
 WB Positive Control Cell Lysates (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
HeLa nuclear extract sc-2120 1000 µg $143
A-431 nuclear extract sc-2122 1000 µg $143
Jurkat nuclear extract sc-2132 1000 µg $143
NIH/3T3 nuclear extract sc-2138 1000 µg $143
HeLa Whole Cell Lysate sc-2200 500 µg/200 µl $104
SW480 nuclear extract sc-2155 1000 µg $143

PMS2 Background Information
The finding that mutations in DNA mismatch repair genes are associated with hereditary nonpolyposis colorectal cancer (HNPCC) has resulted in considerable interest in the understanding of the mechanism of DNA mismatch repair. Initially, inherited mutations in the MSH2 and MLH1 homologs of the bacterial DNA mismatch repair genes MutS and MutL were demonstrated at high frequency in HNPCC and were shown to be associated with microsatellite instability. The demonstration that 10 to 45% of pancreatic, gastric, breast, ovarian and small cell lung cancers also display microsatellite instability has been interpreted to suggest that DNA mismatch repair is not restricted to HNPCC tumors but is a common feature in tumor initiation or progression. Two additional homologs of the prokaryotic MutL gene, designated PMS1 and PMS2, have been identified and shown to be mutated in the germline of HNPCC patients.

PMS2 (349.29.5.2)
Click on image to enlarge
PMS2 (349.29.5.2): sc-56203. Western blot analysis of PMS2 expression in HeLa (A), A-431 (B), HEL 92.1.7 (C) and SW480 (D) nuclear extracts.
Download