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PMS2 anticorps (AA 656-767)

Cet anticorps Lapin Polyclonal détecte spécifiquement PMS2 dans WB et ELISA. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN5693181

Aperçu rapide pour PMS2 anticorps (AA 656-767) (ABIN5693181)

Antigène

Voir toutes PMS2 Anticorps
PMS2 (PMS2 Postmeiotic Segregation Increased 2 (S. Cerevisiae) (PMS2))

Reactivité

  • 58
  • 11
  • 8
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 45
  • 15
Lapin

Clonalité

  • 34
  • 26
Polyclonal

Conjugué

  • 43
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp PMS2 est non-conjugé

Application

  • 38
  • 26
  • 14
  • 14
  • 9
  • 7
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 5
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 656-767

    Fonction

    Anti-PMS2 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-PMS2 Antibody Picoband® (ABIN5693181). Tested in ELISA, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Immunogène

    E. coli-derived human PMS2 recombinant protein (Position: E656-L767).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.5 μg/mL
    ELISA, 0.1-0.5 μg/mL
    1. "Entrez Gene: PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)". 2. Nicolaides NC, Papadopoulos N, Liu B, Wei YF, Carter KC, Ruben SM, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM (Sep 1994). "Mutations of two PMS homologues in hereditary nonpolyposis colon cancer". Nature. 371 (6492): 75-80.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg NaN3.

    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

    4 °C,-20 °C

    Stockage commentaire

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Antigène

    PMS2 (PMS2 Postmeiotic Segregation Increased 2 (S. Cerevisiae) (PMS2))

    Autre désignation

    PMS2

    Sujet

    Synonyms: Mismatch repair endonuclease PMS2 , DNA mismatch repair protein PMS2, PMS1 protein homolog 2, PMS2

    Tissue Specificity: Predominantly expressed in dendritic cells and in DC-residing tissues. Also found in placental macrophages, endothelial cells of placental vascular channels, peripheral blood mononuclear cells, and THP-1 monocytes.

    Background: Mismatch repair endonuclease PMS2 is an enzyme that in humans is encoded by the PMS2 gene. The protein encoded by this gene is a key component of the mismatch repair system that functions to correct DNA mismatches and small insertions and deletions that can occur during DNA replication and homologous recombination. This protein forms heterodimers with the gene product of the mutL homolog 1 (MLH1) gene to form the MutL-alpha heterodimer. The MutL-alpha heterodimer possesses an endonucleolytic activity that is activated following recognition of mismatches and insertion/deletion loops by the MutS-alpha and MutS-beta heterodimers, and is necessary for removal of the mismatched DNA. There is a DQHA (X)2E (X)4E motif found at the C-terminus of the protein encoded by this gene that forms part of the active site of the nuclease. Mutations in this gene have been associated with hereditary nonpolyposis colorectal cancer (HNPCC, also known as Lynch syndrome) and Turcot syndrome.

    Poids moléculaire

    115 kDa

    ID gène

    5395

    UniProt

    P54278

    Pathways

    Réparation de l'ADN, Production of Molecular Mediator of Immune Response
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