PMS1 anticorps (AA 405-619)

N° du produit ABIN3023148

Détail du produit anti-PMS1 anticorps

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

Épitope: AA 405-619

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PMS1 est non-conjugé

Application: Western Blotting (WB)

Séquence: DCLNHQISIG DFGYGHCSSE ISNIDKNTKN AFQDISMSNV SWENSQTEYS KTCFISSVKH TQSENGNKDH IDESGENEEE AGLENSSEIS ADEWSRGNIL KNSVGENIEP VKILVPEKSL PCKVSNNNYP IPEQMNLNED SCNKKSNVID NKSGKVTAYD LLSNRVIKKP MSASALFVQD HRPQFLIENP KTSLEDATLQ IEELWKTLSE EEKLK

Réactivité croisée: Humain

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 405-619 of human PMS1 (NP_000525.1).

Isotype: IgG

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

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.

Conseil sur la manipulation: Avoid freeze / thaw cycles

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: 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.,PMS1,HNPCC3,MLH2,PMSL1,hPMS1,Epigenetics & Nuclear Signaling,DNA Damage & Repair,PMS1

Poids moléculaire: 62 kDa/86 kDa/101 kDa/105 kDa

ID gène: 5378

UniProt: P54277