PMS1 polyclonal, anti-human, mouse, rat
€295.00
In stock
SKU
K003284P
Catalog Number: K003284P
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: WB
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Questions? Contact us!
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: WB
Request Manual
Questions? Contact us!
Background:
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.
Synonyms: HNPCC3, MLH2, PMSL1, hPMS1
Cellular Location: Nucleus
Immunogen:
Recombinant protein of human PMS1
Gene Symbol: PMS1
Gene ID: 5378
Swiss prot: P54277
Calculated MW: 106kDa
Recommended dilution:
WB 1:500-2000
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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.
Synonyms: HNPCC3, MLH2, PMSL1, hPMS1
Cellular Location: Nucleus
Immunogen:
Recombinant protein of human PMS1
Gene Symbol: PMS1
Gene ID: 5378
Swiss prot: P54277
Calculated MW: 106kDa
Recommended dilution:
WB 1:500-2000
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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