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CEP290 antibody (AA 2429-2479)

CEP290 Reactivity: Human WB, IP, IF/ICC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7453386
  • Target See all CEP290 Antibodies
    CEP290 (Centrosomal Protein 290kDa (CEP290))
    Binding Specificity
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2429-2479
    Reactivity
    • 27
    • 8
    • 3
    • 1
    • 1
    Human
    Host
    • 25
    • 2
    Rabbit
    Clonality
    • 27
    Polyclonal
    Conjugate
    • 17
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CEP290 antibody is un-conjugated
    Application
    • 13
    • 13
    • 6
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP), Immunofluorescence (fixed cells) (IF/ICC)
    Purpose
    Rabbit anti-CEP290 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    between AA 2429 and 2479
    Isotype
    IgG
    Top Product
    Discover our top product CEP290 Primary Antibody
  • 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 (CEP290 Products)
    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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