Anticorps Monoclonal anti-PMS1
PMS1 Monoclonal Antibody for WB, IF/ICC, ELISA
Hôte / Isotype
Mouse / IgG2a
Réactivité testée
Humain
Applications
WB, IF/ICC, ELISA
Conjugaison
Non conjugué
CloneNo.
1A6G3
N° de cat : 68413-1-PBS
Synonymes
Galerie de données de validation
Informations sur le produit
68413-1-PBS cible PMS1 dans les applications de WB, IF/ICC, ELISA et montre une réactivité avec des échantillons Humain
Réactivité | Humain |
Hôte / Isotype | Mouse / IgG2a |
Clonalité | Monoclonal |
Type | Anticorps |
Immunogène | PMS1 Protéine recombinante Ag28127 |
Nom complet | PMS1 postmeiotic segregation increased 1 (S. cerevisiae) |
Poids moléculaire observé | 106 kDa |
Numéro d’acquisition GenBank | BC096331 |
Symbole du gène | PMS1 |
Identification du gène (NCBI) | 5378 |
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
PMS1 Homolog 1 is a member of the DNA mismatch repair enzymes (MMREs) which is to eliminate the mismatch of insertions and deletions as a consequence of DNA polymerase errors at DNA synthesis in eukaryotes. PMS1 and MLH1 could form a heterodimer MutLβ that belongs to MMREs (PMID:25619773). In the MMR system, the MutS complex recognizes the DNA mispairs firstly, and then the Mlh1-Pms1 and other associated proteins such as PCNA, RFC, ExoI were recruited, inducing Exonuclease 1 (Exo1)-dependent and -independent MMR pathways (PMID:24981171). Mutations in this gene cause hereditary nonpolyposis colorectal cancer(HNPCC), which is also known as Lynch syndrome. It was reported that PMS1 is a widely expressed protein and located in the nucleus. Alternative splicing allows for 4 isoforms of PMS1 protein.