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TEFM anticorps (Transcription Elongation Factor, Mitochondrial) (Alexa Fluor 594) Primary Antibody

TEFM Reactivité: Humain, Souris, Rat IF (p) Hôte: Lapin Polyclonal Alexa Fluor 594
N° du produit ABIN2810602
$442.20
Plus shipping costs $45.00
100 μL
local_shipping Destination: Etats-Unis
Envoi sous 11 à 16 jours ouvrables
  • Antigène
    TEFM
    Reactivité
    Humain, Souris, Rat
    • 18
    • 14
    • 14
    • 2
    • 1
    • 1
    Hôte
    Lapin
    Clonalité
    Polyclonal
    Conjugué
    Cet anticorp TEFM est conjugé à/à la Alexa Fluor 594
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Application
    Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    • 12
    • 7
    • 3
    • 1
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C17orf42
    Isotype
    IgG
  • Indications d'application
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
    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
    Stockage commentaire
    Store at 4°C
    Date de péremption
    12 months
  • Antigène
    TEFM
    Autre désignation
    C17orf42 (TEFM Antibody Extrait)
    Synonymes
    C17orf42, TEFM, zgc:153083, RGD1306595, transcription elongation factor, mitochondrial, TEFM, tefm, Tefm
    Sujet

    C17orf42 is a 360 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene mapping to human chromosome 17. 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, 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-Dube syndrome and Canavan disease are also associated with chromosome 17.

    Synonyms: Chromosome 17 open reading frame 42, FLJ22729, Hypothetical protein LOC79736, MGC24674, UPF0629 protein C17orf42, TEFM_HUMAN.

    ID gène
    79736
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