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FASTKD1 Antikörper

FASTKD1 Reaktivität: Human, Maus, Ratte IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7263405
  • Target Alle FASTKD1 Produkte
    FASTKD1 (FAST Kinase Domains 1 (FASTKD1))
    Reaktivität
    • 21
    • 14
    • 2
    • 1
    Human, Maus, Ratte
    Wirt
    • 20
    • 1
    Kaninchen
    Klonalität
    • 21
    Polyklonal
    Konjugat
    • 14
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser FASTKD1 Antikörper ist unkonjugiert
    Applikation
    • 13
    • 8
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human FASTKD1 (NP_078898.3).
    Isotyp
    IgG
  • Applikationshinweise
    IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    FASTKD1 (FAST Kinase Domains 1 (FASTKD1))
    Andere Bezeichnung
    FASTKD1 (FASTKD1 Produkte)
    Synonyme
    zgc:77397 antikoerper, fakd1 antikoerper, 5330408N05Rik antikoerper, mKIAA1800 antikoerper, RGD1563531 antikoerper, FAST kinase domains 1 antikoerper, FAST kinase domain-containing protein 1 antikoerper, FAST kinase domains 1 L homeolog antikoerper, fastkd1 antikoerper, fakd1 antikoerper, FASTKD1 antikoerper, Fastkd1 antikoerper, fastkd1.L antikoerper
    Hintergrund
    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.
    Gen-ID
    79675
    UniProt
    Q53R41
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