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FASTKD1 antibody

The Rabbit Polyclonal anti-FASTKD1 antibody has been validated for IHC. It is suitable to detect FASTKD1 in samples from Human, Mouse and Rat.
Catalog No. ABIN7263405

Quick Overview for FASTKD1 antibody (ABIN7263405)

Target

FASTKD1 (FAST Kinase Domains 1 (FASTKD1))

Reactivity

  • 21
  • 14
  • 2
  • 1
Human, Mouse, Rat

Host

  • 20
  • 1
Rabbit

Clonality

  • 21
Polyclonal

Conjugate

  • 14
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FASTKD1 antibody is un-conjugated

Application

  • 13
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human FASTKD1 (NP_078898.3).

    Isotype

    IgG
  • 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

    FASTKD1 (FAST Kinase Domains 1 (FASTKD1))

    Alternative Name

    FASTKD1

    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.

    Gene ID

    79675

    UniProt

    Q53R41
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