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CRX antibody (AA 265-299)

The Rabbit Polyclonal anti-CRX antibody has been validated for WB. It is suitable to detect CRX in samples from Human.
Catalog No. ABIN5647525

Quick Overview for CRX antibody (AA 265-299) (ABIN5647525)

Target

See all CRX Antibodies
CRX (Cone-Rod Homeobox (CRX))

Reactivity

  • 24
  • 23
  • 23
Human

Host

  • 32
  • 4
  • 1
  • 1
Rabbit

Clonality

  • 34
  • 4
Polyclonal

Conjugate

  • 17
  • 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

  • 15
  • 13
  • 13
  • 11
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 265-299

    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
  • 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)

    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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