PMS1 anticorps

N° du produit ABIN5963927

Détail du produit anti-PMS1 anticorps

Antigène: PMS1 (PMS1 Postmeiotic Segregation Increased 1 (S. Cerevisiae) (PMS1))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PMS1 est non-conjugé

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogène: Recombinant protein of human PMS1

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur PMS1

Antigène: PMS1 (PMS1 Postmeiotic Segregation Increased 1 (S. Cerevisiae) (PMS1))

Autre désignation: PMS1 (PMS1 Produits)

Synonymes: anticorps PMSL1, anticorps si:dz72b14.2, anticorps si:dz164h20.2, anticorps PMS1, anticorps DKFZp468M105, anticorps pms1, anticorps HNPCC3, anticorps hPMS1, anticorps PMS1 homolog 1, mismatch repair system component, anticorps PMS1 homolog 1, mismatch repair system component S homeolog, anticorps PMS1, anticorps Pms1, anticorps pms1, anticorps pms1.S

Sujet:

Synonyms: DNA mismatch repair protein PMS1,FLJ98259,HNPCC3,hPMS1,Human homolog of yeast mutL,Mismatch repair gene PMSL1,pms1,PMS1 postmeiotic segregation increased 1 (S. cerevisiae),PMS1 postmeiotic segregation increased 1,PMS1 protein homolog 1,PMS1,PMSL1,Rhabdomyosarcoma antigen MU RMS 40.10B,Rhabdomyosarcoma antigen MU RMS 40.10E

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.

Poids moléculaire:

Observed_MW: 65kDa

Calculated_MW: 62kDa/86kDa/101kDa/105kDa

ID gène: 5378

UniProt: P54277