- Phare
- Validé par KD/KO
Anticorps Monoclonal anti-MLH1
MLH1 Monoclonal Antibody for WB, Indirect ELISA
Hôte / Isotype
Mouse / IgG2a
Réactivité testée
Humain, rat
Applications
WB, Indirect ELISA
Conjugaison
Non conjugué
CloneNo.
2F12C4
N° de cat : 67350-1-PBS
Synonymes
Galerie de données de validation
Informations sur le produit
67350-1-PBS cible MLH1 dans les applications de WB, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat
| Réactivité | Humain, rat | 
| Hôte / Isotype | Mouse / IgG2a | 
| Clonalité | Monoclonal | 
| Type | Anticorps | 
| Immunogène | MLH1 Protéine recombinante Ag27723 | 
| Nom complet | mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) | 
| Masse moléculaire calculée | 756 aa, 85 kDa | 
| Poids moléculaire observé | 85-100 kDa, 40-45 kDa | 
| Numéro d’acquisition GenBank | BC006850 | 
| Symbole du gène | MLH1 | 
| Identification du gène (NCBI) | 4292 | 
| Conjugaison | Non conjugué | 
| Forme | Liquide | 
| Méthode de purification | Purification par protéine A | 
| Tampon de stockage | PBS only | 
| Conditions de stockage | Store at -80°C. 20ul contiennent 0,1% de BSA. | 
Informations générales
MLH1, also named as COCA2, belongs to the DNA mismatch repair mutL/hexB family. It heterodimerizes with PMS2 to form MutL alpha which is a component of the post-replicative DNA mismatch repair system (MMR). MutL 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. MLH1 also implicated in DNA damage signaling, a process which induces cell cycle arrest and can lead to apoptosis in case of major DNA damages. MLH1 heterodimerizes with MLH3 to form MutL gamma which plays a role in meiosis.(PMID: 16873062, PMID: 18206974) Defects in MLH1 are the cause of hereditary non-polyposis colorectal cancer type 2 (HNPCC2). Defects in MLH1 are a cause of mismatch repair cancer syndrome (MMRCS). Defects in MLH1 are a cause of Muir-Torre syndrome (MTS). Defects in MLH1 are a cause of susceptibility to endometrial cancer. Western blot analysis with an MLH1 antibody detected a 85-100 kDa band. Full-length human MLH1 is specifically cleaved into degradation products of 40-45 kDa by caspase-3 (PMID: 15087450, PMID: 19603033). This antibody is specific to MLH1.



