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AGPS Antikörper

Der Kaninchen Polyklonal Anti-AGPS-Antikörper wurde für WB validiert. Er ist geeignet, AGPS in Proben von Human und Maus zu detektieren.
Produktnummer ABIN6566949

Kurzübersicht für AGPS Antikörper (ABIN6566949)

Target

Alle AGPS Antikörper anzeigen
AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Reaktivität

  • 21
  • 17
  • 3
Human, Maus

Wirt

  • 34
  • 3
Kaninchen

Klonalität

  • 34
  • 3
Polyklonal

Konjugat

  • 12
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser AGPS Antikörper ist unkonjugiert

Applikation

  • 13
  • 13
  • 11
  • 11
  • 7
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Aufreinigung

    Affinity purification

    Immunogen

    Recombinant protein of human AGPS

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:1000 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    1 mg/mL

    Buffer

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    AGPS (Alkylglycerone Phosphate Synthase (AGPS))

    Andere Bezeichnung

    AGPS

    Hintergrund

    Synonyms: AAG5,ADAP-S,ADAS,ADAS,ADHAPS,ADPS,Aging associated gene 5 protein,Aging-associated gene 5 protein,aging-associated protein 5,AGPS,ALDHPSY,Alkyl-DHAP synthase,Alkyldihydroxyacetonephosphate synthase,Alkyldihydroxyacetonephosphate synthase,peroxisomal,Alkylglycerone phosphate synthase,Alkylglycerone-phosphate synthase,peroxisomal,RCDP3

    Background: This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome.

    Molekulargewicht

    Observed_MW: 60-73kDa

    Calculated_MW: 72kDa

    Gen-ID

    8540

    UniProt

    O00116

    Pathways

    SARS-CoV-2 Protein Interaktom
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