Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

Lipase A Antikörper

Der Maus Monoklonal anti-Lipase A Antikörper (Klon 9G7F12-7G6D7) (ABIN3210008) detektiert spezifisch Lipase A in WB und ELISA. Dieser Antikörper reagiert spezifisch mit Proben aus Human.
Produktnummer ABIN3210008
1.184,92 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μL
Lieferung nach: Deutschland
Lieferung in 20 bis 27 Werktagen

Kurzübersicht für Lipase A Antikörper (ABIN3210008)

Target

Alle Lipase A (LIPA) Antikörper anzeigen
Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))

Reaktivität

  • 33
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 28
  • 6
Maus

Klonalität

  • 29
  • 6
Monoklonal

Konjugat

  • 20
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Lipase A Antikörper ist unkonjugiert

Applikation

  • 23
  • 15
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA

Klon

9G7F12-7G6D7
  • Aufreinigung

    Purified antibody.

    Immunogen

    LAL antibody was raised in Mouse using a purified recombinant fragment of LAL expressed in E. coli as the immunogen.

    Isotyp

    IgG2a
  • Applikationshinweise

    ELISA: 1:10,000, WB: 1:500-1:2000,
    Optimal conditions should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    Lot specific

    Buffer

    Purified antibody supplied in PBS containing 0.03 % sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium Azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Handhabung

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

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at 4 °C for short term storage. Store at -20 °C for long term storage.
  • Target

    Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))

    Andere Bezeichnung

    LAL

    Hintergrund

    LAL functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides which are taken up by receptor-mediated endocytosis. An inherited deficiency or low activity of human lysosomal acid lipase results in the intralysosomal storage of the respective lipid substrates. So it is also responsible for the rare conditions of Wolman disease and cholesteryl ester storage disease (CESD). As the enzyme is synthesized by all nucleated cells, lipid-laden cells are found in all organs, particularly in liver, spleen, the adrenal and the hemopoietic system, and in the intestine as well as in the lymph nodes, lungs, testes, and ovaries. Synonyms: Monoclonal LAL antibody, Anti-LAL antibody, Lysosomal acid lipase antibody.
Sie sind hier:
Blank Blank Blank Blank
Blank Blank Blank Blank
Chat with us!