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DKC1 antibody

The Rabbit Polyclonal anti-DKC1 antibody has been validated for IHC and IF. It is suitable to detect DKC1 in samples from Human, Mouse and Rat.
Catalog No. ABIN7259883
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$457.98
$538.80
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Quick Overview for DKC1 antibody (ABIN7259883)

Target

See all DKC1 Antibodies
DKC1 (Dyskeratosis Congenita 1, Dyskerin (DKC1))

Reactivity

  • 88
  • 52
  • 44
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 88
  • 3
  • 1
Rabbit

Clonality

  • 61
  • 31
Polyclonal

Conjugate

  • 37
  • 7
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DKC1 antibody is un-conjugated

Application

  • 73
  • 39
  • 31
  • 26
  • 21
  • 13
  • 13
  • 10
  • 10
  • 3
  • 3
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human DKC1 (NP_001354.1).

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200 IF 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

    DKC1 (Dyskeratosis Congenita 1, Dyskerin (DKC1))

    Alternative Name

    DKC1

    Background

    This gene functions in two distinct complexes. It plays an active role in telomerase stabilization and maintenance, as well as recognition of snoRNAs containing H/ACA sequences which provides stability during biogenesis and assembly into H/ACA small nucleolar RNA ribonucleoproteins (snoRNPs). This gene is highly conserved and widely expressed, and may play additional roles in nucleo-cytoplasmic shuttling, DNA damage response, and cell adhesion. Mutations have been associated with X-linked dyskeratosis congenita. Alternative splicing results in multiple transcript variants.

    Gene ID

    1736

    UniProt

    O60832

    Pathways

    Telomere Maintenance
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