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PPT1 Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch PPT1 in WB, IHC (p) und FACS. Er zeigt eine Reaktivität gegenüber Human und Ratte.
Produktnummer ABIN4952244

Kurzübersicht für PPT1 Antikörper (ABIN4952244)

Target

Alle PPT1 Antikörper anzeigen
PPT1 (Palmitoyl-Protein Thioesterase 1 (PPT1))

Reaktivität

  • 54
  • 20
  • 9
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Ratte

Wirt

  • 49
  • 8
Kaninchen

Klonalität

  • 51
  • 6
Polyklonal

Konjugat

  • 38
  • 5
  • 4
  • 4
  • 3
  • 3
Dieser PPT1 Antikörper ist unkonjugiert

Applikation

  • 48
  • 33
  • 29
  • 11
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Aufreinigung

    Antigen affinity

    Immunogen

    Amino acids KEDVYRNHSIFLADINQERGINESYKKNLMALKK of human PPT1 were used as the immunogen for the PPT1 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the PPT1 antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL,IHC (Paraffin): 0.5-1 μg/mL,FACS: 1-3 μg/10^6 cells

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    -20 °C

    Informationen zur Lagerung

    After reconstitution, the PPT1 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    PPT1 (Palmitoyl-Protein Thioesterase 1 (PPT1))

    Andere Bezeichnung

    PPT1

    Hintergrund

    Palmitoyl-protein thioesterase 1 (PPT-1), also known as palmitoyl-protein hydrolase 1, is an enzyme that in humans is encoded by the PPT1 gene. PPT-1 is a member of the palmitoyl protein thioesterase family. The protein encoded by this gene is a small glycoprotein involved in the catabolism of lipid-modified proteins during lysosomal degradation. The encoded enzyme removes thioester-linked fatty acyl groups such as palmitate from cysteine residues. Defects in this gene are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1, or INCL) and neuronal ceroid lipofuscinosis 4 (CLN4). Two transcript variants encoding different isoforms have been found for this gene.

    UniProt

    P50897

    Pathways

    SARS-CoV-2 Protein Interaktom
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