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AGPS antibody (AA 158-384)

This Mouse Monoclonal antibody specifically detects AGPS in WB and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN5540330

Quick Overview for AGPS antibody (AA 158-384) (ABIN5540330)

Target

See all AGPS Antibodies
AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Reactivity

  • 22
  • 17
  • 4
Human

Host

  • 34
  • 4
Mouse

Clonality

  • 34
  • 4
Monoclonal

Conjugate

  • 13
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This AGPS antibody is un-conjugated

Application

  • 13
  • 13
  • 12
  • 10
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
Western Blotting (WB), Flow Cytometry (FACS)

Clone

AGPS-03
  • Binding Specificity

    • 15
    • 5
    • 2
    • 1
    • 1
    • 1
    AA 158-384

    Specificity

    This antibody recognizes AGPS (alkykglycerone phosphate synthase), an peroxisomal enzyme important for lipid biosynthesis.

    Purification

    Protein-A affinity chromatography (>95% pure by SDS-PAGE)

    Immunogen

    Recombinant human AGPS (amino acids 158-384)

    Isotype

    IgG2a
  • Application Notes

    Flow cytometry. Western blot.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    95 % pure by SDS-PAGE) Buffer System: Phosphate buffered saline (PBS) Preservatives: 15 mM sodium azide, approx. pH 7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C

    Storage Comment

    Store undiluted at 2-8°C. DO NOT FREEZE! Shelf life: one year from despatch.

    Expiry Date

    12 months
  • Target

    AGPS (Alkylglycerone Phosphate Synthase (AGPS))

    Alternative Name

    agps,aag5

    Background

    AGPS (alkylglycerone phosphate synthase), is an enzyme that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetone phosphate (acyl-DHAP) is converted to alkyl-DHAP by addition of a long chain alcohol and removal of a long-chain acid anion. The protein is localized to the inner side of the peroxisomal membrane and requires FAD as a cofactor. Mutations in AGPS gene have been associated with type 3 of rhizomelic chondrodysplasia punctata (RCDP3), and Zellweger syndrome. Higher expression of AGPS was observed in BCR/ABL positive leukemias and it was also described to be associated with higher risk of relapse.

    UniProt

    O00116

    Pathways

    SARS-CoV-2 Protein Interactome
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