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MSH6 anticorps (AA 357-388)

L’anticorps Lapin Polyclonal anti-MSH6 a été validé pour WB, ELISA, IF, FACS et ICC. Il convient pour détecter MSH6 dans des échantillons de Humain.
N° du produit ABIN7601449

Aperçu rapide pour MSH6 anticorps (AA 357-388) (ABIN7601449)

Antigène

Voir toutes MSH6 Anticorps
MSH6 (MutS Homolog 6 (E. Coli) (MSH6))

Reactivité

  • 109
  • 36
  • 28
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 59
  • 47
  • 3
Lapin

Clonalité

  • 63
  • 45
  • 1
Polyclonal

Conjugué

  • 53
  • 7
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
Cet anticorp MSH6 est non-conjugé

Application

  • 75
  • 59
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  • 33
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  • 14
  • 13
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Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS), Immunocytochemistry (ICC)
  • Épitope

    • 38
    • 15
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
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    • 1
    • 1
    • 1
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    • 1
    • 1
    • 1
    AA 357-388

    Fonction

    Anti-MSH6 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-MSH6 Antibody Picoband® (ABIN7601449). Tested in ELISA, Flow Cytometry, IF, ICC, WB applications. This antibody reacts with Human. 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.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human MSH6 recombinant protein (Position: D357-H388).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.25 μg/mL, Human
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Kariola, R., Raevaara, T. E., Lonnqvist, K. E., Nystrom-Lahti, M. Functional analysis of MSH6 mutations linked to kindreds with putative hereditary non-polyposis colorectal cancer syndrome. Hum. Molec. Genet. 11: 1303-1310, 2002. 2. Verma, L., Kane, M. F., Brassett, C., Schmeits, J., Evans, D. G. R., Kolodner, R. D., Maher, E. R. Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer. J. Med. Genet. 36: 678-682, 1999.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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 freezing and thawing.
  • Antigène

    MSH6 (MutS Homolog 6 (E. Coli) (MSH6))

    Autre désignation

    MSH6

    Sujet

    Synonyms: UDP-glucose 4-epimerase

    Tissue Specificity: Colocalizes with SMARCA4/BRG1 in E-cadherin-negative cells from established lines, and stroma of normal colon as well as in de-differentiated epithelial cells at the invasion front of colorectal carcinomas (at protein level). Expressed in heart and skeletal muscle, but not in liver, spleen, or pancreas.

    Background: MSH6 or mutS homolog 6 is a gene that codes for DNA mismatch repair protein Msh6 in the budding yeast Saccharomyces cerevisiae. This gene encodes a member of the DNA mismatch repair MutS family. In E. coli, the MutS protein helps in the recognition of mismatched nucleotides prior to their repair. A highly conserved region of approximately 150 aa, called the Walker-A adenine nucleotide binding motif, exists in MutS homologs. The encoded protein heterodimerizes with MSH2 to form a mismatch recognition complex that functions as a biional molecular switch that exchanges ADP and ATP as DNA mismatches are bound and dissociated. Mutations in this gene may be associated with hereditary nonpolyposis colon cancer, colorectal cancer, and endometrial cancer. Transcripts variants encoding different isoforms have been described.

    Poids moléculaire

    160 kDa

    ID gène

    2956

    UniProt

    P52701

    Pathways

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