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TEX37 anticorps

TEX37 Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7244336
  • Antigène Tous les produits TEX37
    TEX37 (Testis Expressed 37 (TEX37))
    Reactivité
    • 17
    • 1
    Humain
    Hôte
    • 17
    Lapin
    Clonalité
    • 17
    Polyclonal
    Conjugué
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp TEX37 est non-conjugé
    Application
    • 10
    • 8
    • 8
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human TEX37
    Isotype
    IgG
  • Indications d'application
    IHC 1:30-150, ELISA 1:2000-10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.8 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    TEX37 (Testis Expressed 37 (TEX37))
    Autre désignation
    TEX37 (TEX37 Produits)
    Synonymes
    anticorps C11H2orf51, anticorps TSC21, anticorps 1700011F03Rik, anticorps C2orf51, anticorps testis expressed 37, anticorps TEX37, anticorps Tex37
    Sujet
    The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
    NCBI Accession
    NP_689883
    UniProt
    Q96LM6
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