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TMIGD1 anticorps (AA 160-200)

L’anticorps Lapin Polyclonal anti-TMIGD1 a été validé pour WB, IHC (p) et IF (p). Il convient pour détecter TMIGD1 dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN1387070

Aperçu rapide pour TMIGD1 anticorps (AA 160-200) (ABIN1387070)

Antigène

Voir toutes TMIGD1 Anticorps
TMIGD1 (Transmembrane and Immunoglobulin Domain Containing 1 (TMIGD1))

Reactivité

Humain, Souris, Rat

Hôte

  • 1
  • 1
Lapin

Clonalité

  • 1
  • 1
Polyclonal

Conjugué

  • 2
Cet anticorp TMIGD1 est non-conjugé

Application

  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Épitope

    • 1
    • 1
    AA 160-200

     Réactivité croisée

    Humain, Souris, Rat

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human TMIGD1

    Isotype

    IgG
  • Indications d'application

    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Agent conservateur

    ProClin

    Précaution d'utilisation

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    Date de péremption

    12 months
  • Antigène

    TMIGD1 (Transmembrane and Immunoglobulin Domain Containing 1 (TMIGD1))

    Autre désignation

    TMIGD1

    Sujet

    Synonyms: TMIGD, UNQ9372, Transmembrane and immunoglobulin domain-containing protein 1, TMIGD1, UNQ9372/PRO34164

    Background: Chromosome 17 makes up over 2.5 % of the human genome with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, though specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. Chromosome 17 is also linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth. Alexander disease, Birt-Hogg-Dub? syndrome and Canavan disease are also associated with chromosome 17.

    ID gène

    388364

    UniProt

    Q6UXZ0
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