PMS2 Rekombinanter Antikörper
PMS2 Rekombinant Antikörper für WB, IHC, FC (Intra), Indirect ELISA
Wirt / Isotyp
Kaninchen / IgG
Getestete Reaktivität
human
Anwendung
WB, IHC, FC (Intra), Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
242455F8
Kat-Nr. : 84894-5-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
84894-5-PBS bindet in WB, IHC, FC (Intra), Indirect ELISA PMS2 und zeigt Reaktivität mit human
| Getestete Reaktivität | human |
| Wirt / Isotyp | Kaninchen / IgG |
| Klonalität | Rekombinant |
| Typ | Antikörper |
| Immunogen | PMS2 fusion protein Ag33508 |
| Vollständiger Name | PMS2 postmeiotic segregation increased 2 (S. cerevisiae) |
| Berechnetes Molekulargewicht | 862 aa, 96 kDa |
| Beobachtetes Molekulargewicht | 117 kDa |
| GenBank-Zugangsnummer | BC093921 |
| Gene symbol | PMS2 |
| Gene ID (NCBI) | 5395 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein A purfication |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
PMS2, also named as PMSL2, belongs to the DNA mismatch repair mutL/hexB family. It is a component of the post-replicative DNA mismatch repair system (MMR). It heterodimerizes with MLH1 to form MutL alpha. MulL alpha (MLH1-PMS2) interacts physically with the clamp loader subunits of DNA polymerase III, suggesting that it may play a role to recruit the DNA polymerase III to the site of the MMR. It also implicated in DNA damage signaling, a process which induces cell cycle arrest and can lead to apoptosis in case of major DNA damages. (PMID: 16873062, PMID: 18206974) Defects in PMS2 are the cause of hereditary non-polyposis colorectal cancer type 4 (HNPCC4). Defects in PMS2 are a cause of mismatch repair cancer syndrome (MMRCS).











