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KRT16 antibody

This Rabbit Polyclonal antibody specifically detects KRT16 in WB, IHC and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7242044

Quick Overview for KRT16 antibody (ABIN7242044)

Target

See all KRT16 Antibodies
KRT16 (Keratin 16 (KRT16))

Reactivity

  • 133
  • 36
  • 35
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 78
  • 53
  • 2
Rabbit

Clonality

  • 73
  • 60
Polyclonal

Conjugate

  • 54
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  • 7
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This KRT16 antibody is un-conjugated

Application

  • 64
  • 62
  • 28
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  • 14
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  • 5
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Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Synthetic peptide of human KRT16

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 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

    KRT16 (Keratin 16 (KRT16))

    Alternative Name

    CK-16

    Background

    The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains and are clustered in a region of chromosome 17q12-q21. This keratin has been coexpressed with keratin 14 in a number of epithelial tissues, including esophagus, tongue, and hair follicles. Mutations in this gene are associated with type 1 pachyonychia congenita, non-epidermolytic palmoplantar keratoderma and unilateral palmoplantar verrucous nevus.

    Molecular Weight

    51 kDa

    NCBI Accession

    NP_005548

    UniProt

    P08779
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