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CEP290 antibody (AA 2429-2479)

The Rabbit Polyclonal anti-CEP290 antibody has been validated for IF/ICC. It is suitable to detect CEP290 in samples from Human.
Catalog No. ABIN7448387

Quick Overview for CEP290 antibody (AA 2429-2479) (ABIN7448387)

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
  • 3
  • 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
  • 16
  • 13
  • 13
  • 6
  • 5
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
Immunofluorescence (fixed cells) (IF/ICC)
  • Binding Specificity

    • 15
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2429-2479

    Purpose

    Rabbit anti-CEP290 IHC Antibody, affinity purified

    Predicted Reactivity

    Horse,Orangutan,Monkey,Gorilla,Northern white-cheeked gibbon,Small-eared galago,African elephant

    Purification

    Affinity Purified

    Immunogen

    Between AA 2429 and 2479

    Isotype

    IgG
  • Application Notes

    1:100 - 1:500

    Restrictions

    For Research Use only
  • Concentration

    500 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 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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