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CA2 Antikörper

Dieses Anti-CA2-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von CA2 in WB, IHC (p) und FACS. Geeignet für Human, Ratte und Maus.
Produktnummer ABIN5647703

Kurzübersicht für CA2 Antikörper (ABIN5647703)

Target

Alle CA2 Antikörper anzeigen
CA2 (Carbonic Anhydrase II (CA2))

Reaktivität

  • 104
  • 51
  • 50
  • 15
  • 12
  • 12
  • 12
  • 10
  • 10
  • 5
  • 4
  • 4
  • 3
  • 2
  • 1
Human, Ratte, Maus

Wirt

  • 156
  • 16
  • 7
  • 3
  • 1
Kaninchen

Klonalität

  • 155
  • 27
Polyklonal

Konjugat

  • 97
  • 29
  • 10
  • 10
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser CA2 Antikörper ist unkonjugiert

Applikation

  • 148
  • 96
  • 55
  • 45
  • 40
  • 16
  • 13
  • 13
  • 12
  • 8
  • 8
  • 7
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Aufreinigung

    Antigen affinity purified

    Immunogen

    Amino acids S2-K260 from the human protein were used as the immunogen for the CA2 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Western blot: 0.5-1 μg/mL,IHC (FFPE): 1-2 μg/mL,FACS: 1-3 μg/10^6 cells

    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

    Prior to reconstitution, store at 4°C. After reconstitution, the CA2 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

    CA2 (Carbonic Anhydrase II (CA2))

    Andere Bezeichnung

    CA2 / Carbonic Anhydrase II

    Hintergrund

    CA2 is a cytosolic enzyme with the highest activity among all known CAs. The carbonic anhydrases (ACs) form a family of enzymes that catalyze the rapid interconversion of carbon dioxide and water to bicarbonate and protons (or vice versa), a reversible reaction that occurs relatively slowly in the absence of a catalyst. Mutations in the CA2 gene result in the CA II deficiency syndrome, an autosomal recessive disorder that produces osteopetrosis, renal tubular acidosis and cerebral calcification. This gene is mapped to 8q22.

    UniProt

    P00918
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