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HPS3 Antikörper (C-Term)

Der Ziege Polyklonal Anti-HPS3-Antikörper wurde für WB validiert. Er ist geeignet, HPS3 in Proben von Human zu detektieren.
Produktnummer ABIN374450

Kurzübersicht für HPS3 Antikörper (C-Term) (ABIN374450)

Target

Alle HPS3 Antikörper anzeigen
HPS3 (Hermansky-Pudlak Syndrome 3 (HPS3))

Reaktivität

  • 19
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 17
  • 1
  • 1
Ziege

Klonalität

  • 19
Polyklonal

Konjugat

  • 14
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser HPS3 Antikörper ist unkonjugiert

Applikation

  • 19
  • 10
  • 4
  • 2
  • 2
  • 2
Western Blotting (WB)
  • Bindungsspezifität

    • 8
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    C-Term

    Sequenz

    PYLLYCSRKK PLT

    Spezifität

    This antibody recognizes HPS3/Cocoa

    Kreuzreaktivität (Details)

    Species reactivity (tested):Human.

    Aufreinigung

    Ammonium Sulphate Precipitation followed by antigen Affinity Chromatography using the immunizing peptide.

    Immunogen

    Peptide from the C Terminus of the protein sequence according to NP_115759
  • Applikationshinweise

    Peptide ELISA: > 1/32,000. Western Blot: 1-3 μg/mL. Detects a band of Approx 110 kDa in A431 cell lysate(Predicted Molecular Weight: 114 kDa).
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    0.5 mg/mL

    Buffer

    Tris saline, pH 7.3 containing 0.02 % Sodium Azide as preservative and 0.5 % BSA as stabilizer.

    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 freezing and thawing.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store the antibody (in aliquots) at -20 °C.
  • Target

    HPS3 (Hermansky-Pudlak Syndrome 3 (HPS3))

    Andere Bezeichnung

    HPS3

    Hintergrund

    HPS3 is involved in early stages of melanosome biogenesis and maturation. Defects in HPS3 are the cause of the cocoa (coa) mutant, and of Hermansky-Pudlak syndrome type 3 (HPS3). HPS3 is an autosomal recessive disorder, characterized by oculocutaneous albinism, bleeding due to platelet storage pool deficiency, and lysosomal storage defects. This syndrome results from defects of diverse cytoplasmic organelles including melanosomes, platelet dense granules and lysosomes. Ceroid storage in the lungs is associated with pulmonary fibrosis, a common cause of premature death in individuals with HPS.Synonyms: Hermansky-Pudlak syndrome 3

    Gen-ID

    84343

    NCBI Accession

    NP_115759

    UniProt

    Q969F9
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