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TTC38 Antikörper

TTC38 Reaktivität: Human, Maus ELISA, IHC, WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7253539
  • Target Alle TTC38 Antikörper anzeigen
    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))
    Reaktivität
    Human, Maus
    Wirt
    • 13
    • 1
    Kaninchen
    Klonalität
    • 14
    Polyklonal
    Konjugat
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TTC38 Antikörper ist unkonjugiert
    Applikation
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Fusion protein of human TTC38
    Isotyp
    IgG
    Top Product
    Discover our top product TTC38 Primärantikörper
  • Applikationshinweise
    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.5 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))
    Andere Bezeichnung
    TTC38 (TTC38 Produkte)
    Synonyme
    9030019H09 antikoerper, fb96d09 antikoerper, si:ch211-249g22.2 antikoerper, wu:fb96d09 antikoerper, zgc:112407 antikoerper, tetratricopeptide repeat domain 38 antikoerper, tetratricopeptide repeat domain 38 S homeolog antikoerper, TTC38 antikoerper, Ttc38 antikoerper, ttc38.S antikoerper, ttc38 antikoerper
    Hintergrund
    TTC38 (tetratricopeptide repeat domain 38) is a 469 amino acid protein that contains three TPR repeats and belongs to the TTC38 family. The gene that encodes TTC38 consists of over 26,000 bases and maps to 22q13. Housing over 500 genes, chromosome 22 is the second smallest chromosome in the human genome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. In addition, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
    Molekulargewicht

    Observed_MW: Refer to figures

    Calculated_MW: 53 kDa

    UniProt
    Q5R3I4
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