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KRT81 antibody

KRT81 Reactivity: Human IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7260917
  • Target See all KRT81 Antibodies
    KRT81 (Keratin 81 (KRT81))
    Reactivity
    • 40
    • 18
    • 1
    Human
    Host
    • 34
    • 5
    • 1
    Rabbit
    Clonality
    • 36
    • 4
    Polyclonal
    Conjugate
    • 19
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This KRT81 antibody is un-conjugated
    Application
    • 36
    • 16
    • 14
    • 14
    • 10
    • 7
    • 5
    • 5
    • 4
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human KRT81 (NP_002272.2).
    Isotype
    IgG
    Top Product
    Discover our top product KRT81 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    KRT81 (Keratin 81 (KRT81))
    Alternative Name
    KRT81 (KRT81 Products)
    Background
    The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. All hair keratins are expressed in the hair follicle, this hair keratin, as well as KRTHB3 and KRTHB6, is found primarily in the hair cortex. Mutations in this gene and KRTHB6 have been observed in patients with a rare dominant hair disease, monilethrix.
    Gene ID
    3887
    UniProt
    Q14533
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