PMS1 (NM_000534) Human Recombinant Protein
CAT#: TP762279
Purified recombinant protein of Human PMS1 postmeiotic segregation increased 1 (S. cerevisiae) (PMS1), transcript variant 1, Glu323-Ser423, with N-terminal His-ABP tag, expressed in E.coli, 50ug
View other "PMS1" proteins (2)
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CNY 1,950.00
CNY 1,999.00
CNY 2,700.00
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding the region(Glu323-Ser423) of PMS1
|
Tag | N-His-ABP (Albumin-Binding Protein) |
Predicted MW | 26.3 kDa |
Concentration | >0.05 µg/µL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 50 mM Tris-HCl, pH 8.0, 8 M urea |
Note | For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process. |
Storage | Store at -80°C after receiving vials. |
Stability | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_000525 |
Locus ID | 5378 |
UniProt ID | P54277 |
Refseq Size | 3239 |
Cytogenetics | 2q32.2 |
Refseq ORF | 2796 |
Synonyms | HNPCC3; hPMS1; MLH2; PMSL1 |
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, Jul 2008] |
Protein Families | Druggable Genome, Transcription Factors |
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