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CRX Antikörper (AA 265-299)

Der Kaninchen Polyklonal Anti-CRX-Antikörper wurde für WB validiert. Er ist geeignet, CRX in Proben von Human zu detektieren.
Produktnummer ABIN5647525

Kurzübersicht für CRX Antikörper (AA 265-299) (ABIN5647525)

Target

Alle CRX Antikörper anzeigen
CRX (Cone-Rod Homeobox (CRX))

Reaktivität

  • 24
  • 23
  • 23
Human

Wirt

  • 32
  • 4
  • 1
  • 1
Kaninchen

Klonalität

  • 34
  • 4
Polyklonal

Konjugat

  • 17
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser CRX Antikörper ist unkonjugiert

Applikation

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

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

    Aufreinigung

    Antigen affinity purified

    Immunogen

    Amino acids 265-299 (DSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL) from the human protein were used as the immunogen for the CRX antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the CRX antibody should be determined by the researcher.\. WB: 0.5-1 μg/mL

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    -20 °C

    Informationen zur Lagerung

    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))

    Andere Bezeichnung

    CRX (Cone-rod homeobox)

    Hintergrund

    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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