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ACP6 Antikörper

Dieses Anti-ACP6-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von ACP6 in IHC und ELISA. Geeignet für Human.
Produktnummer ABIN7237330

Kurzübersicht für ACP6 Antikörper (ABIN7237330)

Target

Alle ACP6 Antikörper anzeigen
ACP6 (Acid Phosphatase 6, Lysophosphatidic (ACP6))

Reaktivität

  • 25
  • 9
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 28
  • 2
Kaninchen

Klonalität

  • 30
Polyklonal

Konjugat

  • 20
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ACP6 Antikörper ist unkonjugiert

Applikation

  • 20
  • 10
  • 7
  • 6
  • 6
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant protein of human ACP6

    Isotyp

    IgG
  • Applikationshinweise

    IHC 1:50-1:200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.2 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    ACP6 (Acid Phosphatase 6, Lysophosphatidic (ACP6))

    Andere Bezeichnung

    ACP6

    Hintergrund

    Lysophosphatidic acid phosphatase type 6 (ACP6), also designated acid phosphatase-like protein 1 (ACPL1) or lysophosphatidic acid phosphatase (LPAP), is a 428 amino acid secreted protein that hydrolyzes lysophosphatidic acid to monoacylglycerol. ACP6 is highly expressed in kidney, heart, small intestine, muscle, liver, prostate, testis, ovary and exists as two isoforms as a result of alternative splicing events. The gene encoding ACP6 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene of human chromosome 1, which encodes lamin A. Stickler syndrome, Parkinsons, Gaucher disease, familial adenomatous polyposis and Usher syndrome are also associated with chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

    UniProt

    Q9NPH0
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