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PGAP1 antibody (AA 166-904)

The Rabbit Polyclonal anti-PGAP1 antibody is suitable to detect PGAP1 in samples from Human. It has been validated for WB, ELISA and FACS.
Catalog No. ABIN7871160
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for PGAP1 antibody (AA 166-904) (ABIN7871160)

Target

See all PGAP1 Antibodies
PGAP1 (Post-GPI Attachment To Proteins 1 (PGAP1))

Reactivity

  • 9
  • 5
  • 4
  • 2
Human

Host

  • 6
  • 3
Rabbit

Clonality

  • 7
  • 2
Polyclonal

Conjugate

  • 9
This PGAP1 antibody is un-conjugated

Application

  • 7
  • 7
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 166-904

    Purpose

    PGAP1 Antibody

    Purification

    Antigen affinity chromatography

    Immunogen

    An E.coli-derived human recombinant protein (amino acids K166-R904) was used as the immunogen for the PGAP1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the PGAP1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

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

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the PGAP1 Antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    PGAP1 (Post-GPI Attachment To Proteins 1 (PGAP1))

    Alternative Name

    PGAP1

    Background

    Post-GPI attachment to proteins 1 is a protein that in humans is encoded by the PGAP1 gene. The protein encoded by this gene functions early in the glycosylphosphatidylinositol (GPI) biosynthetic pathway, catalyzing the inositol deacylation of GPI. The encoded protein is required for the production of GPI that can attach to proteins, and this may be an important factor in the transport of GPI-anchored proteins from the endoplasmic reticulum to the Golgi. Defects in this gene are a cause an autosomal recessive form of cognitive impairment.

    UniProt

    Q75T13

    Pathways

    Sensory Perception of Sound, Inositol Metabolic Process
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