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COX3 Antikörper

Der Kaninchen Polyklonal Anti-COX3-Antikörper wurde für WB und ELISA validiert. Er ist geeignet, COX3 in Proben von Human zu detektieren.
Produktnummer ABIN2459381

Kurzübersicht für COX3 Antikörper (ABIN2459381)

Target

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

Reaktivität

  • 22
  • 18
  • 18
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
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA
  • Aufreinigung

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human COX3.
  • Applikationshinweise

    COX3 antibody can be used for detection of COX3 by ELISA at 1:1562500. COX3 antibody can be used for detection of COX3 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Konzentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handhabung

    As with any antibody avoid repeat freeze-thaw cycles.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store COX3 antibody 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

    Gen-ID

    4514

    NCBI Accession

    NP_536849

    UniProt

    P00414
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