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CEP290 antibody (AA 2429-2479)

This anti-CEP290 antibody is a Rabbit Polyclonal antibody detecting CEP290 in WB, IP and IF/ICC. Suitable for Human.
Catalog No. ABIN7453386

Quick Overview for CEP290 antibody (AA 2429-2479) (ABIN7453386)

Target

See all CEP290 Antibodies
CEP290 (Centrosomal Protein 290kDa (CEP290))

Reactivity

  • 29
  • 25
  • 3
  • 1
  • 1
Human

Host

  • 42
  • 2
Rabbit

Clonality

  • 44
Polyclonal

Conjugate

  • 20
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  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CEP290 antibody is un-conjugated

Application

  • 17
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  • 13
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  • 6
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  • 5
  • 4
  • 4
  • 2
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Western Blotting (WB), Immunoprecipitation (IP), Immunofluorescence (fixed cells) (IF/ICC)
  • Binding Specificity

    • 15
    • 5
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    • 2
    • 2
    • 2
    • 1
    • 1
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    • 1
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    • 1
    AA 2429-2479

    Purpose

    Rabbit anti-CEP290 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 2429 and 2479

    Isotype

    IgG
  • Application Notes

    ICC-IF: 1:250 - 1:1,000. Formaldehyde fixation is recommended. Permeabilization with Triton-X 100 is recommended for formaldehyde-fixed cells.

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

    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

    4 °C

    Expiry Date

    12 months
  • Target

    CEP290 (Centrosomal Protein 290kDa (CEP290))

    Alternative Name

    CEP290

    Background

    Background: Centrosomal protein 290 (CEP290) is a member of the nephrocystins, a family of proteins involved in renal cystic diseases. CEP290 and the nephrocystins appear to play a role in cilia and basal body function. Loss-of-function mutations in CEP290 result in Joubert syndrome and related disorders characterized by brain malformations, developmental delay, ataxia, irregular breathing, renal disease, and hepatic fibrosis.

    Gene ID

    80184

    NCBI Accession

    NP_079390

    UniProt

    O15078

    Pathways

    cAMP Metabolic Process, M Phase
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