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COX3 Antikörper (C-Term)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch COX3 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN635599

Kurzübersicht für COX3 Antikörper (C-Term) (ABIN635599)

Target

Alle COX3 (COX-3) Antikörper anzeigen
COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))

Reaktivität

  • 23
  • 18
  • 17
Human

Wirt

  • 34
  • 2
Kaninchen

Klonalität

  • 34
  • 2
Polyklonal

Konjugat

  • 14
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser COX3 Antikörper ist unkonjugiert

Applikation

  • 34
  • 13
  • 13
  • 13
  • 4
  • 4
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 15
    • 9
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Spezifität

    COX3 antibody was raised against the C terminal of COX3

    Aufreinigung

    Affinity purified

    Immunogen

    COX3 antibody was raised using the C terminal of COX3 corresponding to a region with amino acids FESPFTISDGIYGSTFFVATGFHGLHVIIGSTFLTICFIRQLMFHFTSKH
  • Applikationshinweise

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Kommentare

    COX3 Blocking Peptide, catalog no. 33R-2880, is also available for use as a blocking control in assays to test for specificity of this COX3 antibody

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of COX3 antibody in PBS

    Konzentration

    Lot specific

    Buffer

    PBS

    Handhabung

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))

    Andere Bezeichnung

    COX3

    Hintergrund

    COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.

    Molekulargewicht

    29 kDa (MW of target protein)
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