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CEP164 antibody (AA 10-903)

The Rabbit Polyclonal anti-CEP164 antibody (ABIN7869718) specifically detects CEP164 in WB, ELISA, FACS and IF. The antibody is reactive with Human samples.
Catalog No. ABIN7869718
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for CEP164 antibody (AA 10-903) (ABIN7869718)

Target

See all CEP164 Antibodies
CEP164 (Centrosomal Protein 164kDa (CEP164))

Reactivity

  • 21
  • 3
  • 2
  • 1
Human

Host

  • 20
  • 1
Rabbit

Clonality

  • 20
  • 1
Polyclonal

Conjugate

  • 13
  • 2
  • 2
  • 2
  • 1
  • 1
This CEP164 antibody is un-conjugated

Application

  • 17
  • 14
  • 11
  • 6
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunofluorescence (IF)
  • Binding Specificity

    • 10
    • 4
    • 4
    • 1
    • 1
    AA 10-903

    Purpose

    CEP164 Antibody / Centrosomal protein of 164 kDa

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids D10-R903) was used as the immunogen for the CEP164 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the CEP164 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the CEP164 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    CEP164 (Centrosomal Protein 164kDa (CEP164))

    Alternative Name

    CEP164

    Background

    Centrosomal protein of 164 kDa, also known as CEP164, is a protein that in humans is encoded by the CEP164 gene. This gene encodes a centrosomal protein involved in microtubule organization, DNA damage response, and chromosome segregation. The encoded protein is required for assembly of primary cilia and localizes to mature centrioles. Defects in this gene are a cause of nephronophthisis-related ciliopathies. Two transcript variants encoding different isoforms have been found for this gene.

    UniProt

    Q9UPV0

    Pathways

    M Phase
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