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AGPS antibody

The Rabbit Polyclonal anti-AGPS antibody has been validated for WB. It is suitable to detect AGPS in samples from Human and Mouse.
Catalog No. ABIN6566949

Quick Overview for AGPS antibody (ABIN6566949)

Target

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

Reactivity

  • 21
  • 17
  • 3
Human, Mouse

Host

  • 34
  • 3
Rabbit

Clonality

  • 34
  • 3
Polyclonal

Conjugate

  • 12
  • 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
  • 11
  • 11
  • 7
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Purification

    Affinity purification

    Immunogen

    Recombinant protein of human AGPS

    Isotype

    IgG
  • Application Notes

    WB 1:1000 - 1:2000

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    AGPS (Alkylglycerone Phosphate Synthase (AGPS))

    Alternative Name

    AGPS

    Background

    Synonyms: AAG5,ADAP-S,ADAS,ADAS,ADHAPS,ADPS,Aging associated gene 5 protein,Aging-associated gene 5 protein,aging-associated protein 5,AGPS,ALDHPSY,Alkyl-DHAP synthase,Alkyldihydroxyacetonephosphate synthase,Alkyldihydroxyacetonephosphate synthase,peroxisomal,Alkylglycerone phosphate synthase,Alkylglycerone-phosphate synthase,peroxisomal,RCDP3

    Background: This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome.

    Molecular Weight

    Observed_MW: 60-73kDa

    Calculated_MW: 72kDa

    Gene ID

    8540

    UniProt

    O00116

    Pathways

    SARS-CoV-2 Protein Interactome
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