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PMS1
PMS1 homolog 1, mismatch repair system componentMLH2, PMSL1
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, Jul 2008]
Top validated antibodies |
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| NSJ Bioreagents |  V9715 |
Monoclonal |
EL
ICC
FC
PA
OA
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| Invitrogen Antibodies | 5378-MSM1-P0 |
Monoclonal |
EL
ICC
IP
FC
OA
|
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| Santa Cruz Biotechnology | sc-615 |
2 references | Polyclonal (Antigen purified) |
WB
IHC
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| Proteintech Group | 10859-1-AP |
2 references | Polyclonal |
EL
IHC
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| Antibodies.com | A277752 |
Monoclonal |
EL
ICC
IP
FC
|
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