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PPT1 antibody

This Rabbit Polyclonal antibody specifically detects PPT1 in WB, IHC (p) and FACS. It exhibits reactivity toward Human and Rat.
Catalog No. ABIN4952244
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 3 Business Days

Quick Overview for PPT1 antibody (ABIN4952244)

Target

See all PPT1 Antibodies
PPT1 (Palmitoyl-Protein Thioesterase 1 (PPT1))

Reactivity

  • 55
  • 21
  • 10
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Rat

Host

  • 49
  • 9
Rabbit

Clonality

  • 51
  • 7
Polyclonal

Conjugate

  • 39
  • 5
  • 4
  • 4
  • 3
  • 3
This PPT1 antibody is un-conjugated

Application

  • 47
  • 33
  • 27
  • 12
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Purification

    Antigen affinity

    Immunogen

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

    Isotype

    IgG
  • Application Notes

    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

    Restrictions

    For Research Use only
  • Buffer

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

    Storage

    -20 °C

    Storage Comment

    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))

    Alternative Name

    PPT1

    Background

    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 Interactome
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