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CRX antibody (AA 265-299)

CRX Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5647525
  • Target See all CRX Antibodies
    CRX (Cone-Rod Homeobox (CRX))
    Binding Specificity
    • 15
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 265-299
    Reactivity
    • 24
    • 23
    • 22
    Human
    Host
    • 31
    • 4
    • 1
    • 1
    Rabbit
    Clonality
    • 34
    • 3
    Polyclonal
    Conjugate
    • 16
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CRX antibody is un-conjugated
    Application
    • 14
    • 13
    • 13
    • 11
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity purified
    Immunogen
    Amino acids 265-299 (DSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL) from the human protein were used as the immunogen for the CRX antibody.
    Isotype
    IgG
    Top Product
    Discover our top product CRX Primary Antibody
  • Application Notes
    Optimal dilution of the CRX antibody should be determined by the researcher.\. WB: 0.5-1 μg/mL
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Storage
    -20 °C
    Storage Comment
    After reconstitution, the CRX antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target
    CRX (Cone-Rod Homeobox (CRX))
    Alternative Name
    CRX (Cone-rod homeobox) (CRX Products)
    Background
    Cone-rod homeobox protein is a protein that in humans is encoded by the CRX gene. The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.
    UniProt
    O43186
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