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FASTKD1 antibody

FASTKD1 Reactivity: Human ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7236968
  • Target See all FASTKD1 products
    FASTKD1 (FAST Kinase Domains 1 (FASTKD1))
    Reactivity
    • 22
    • 15
    • 2
    • 2
    Human
    Host
    • 21
    • 1
    Rabbit
    Clonality
    • 22
    Polyclonal
    Conjugate
    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FASTKD1 antibody is un-conjugated
    Application
    • 13
    • 8
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human FASTKD1
    Isotype
    IgG
  • Application Notes
    IHC 1:100-1:300
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FASTKD1 (FAST Kinase Domains 1 (FASTKD1))
    Alternative Name
    FASTKD1 (FASTKD1 Products)
    Synonyms
    zgc:77397 antibody, fakd1 antibody, 5330408N05Rik antibody, mKIAA1800 antibody, RGD1563531 antibody, FAST kinase domains 1 antibody, FAST kinase domain-containing protein 1 antibody, FAST kinase domains 1 L homeolog antibody, fastkd1 antibody, fakd1 antibody, FASTKD1 antibody, Fastkd1 antibody, fastkd1.L antibody
    Background
    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.
    UniProt
    Q53R41
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