AGPS antibody

Catalog No. ABIN2854324

This Rabbit Polyclonal antibody specifically detects AGPS in WB. It exhibits reactivity toward Human.

Quick Overview for AGPS antibody (ABIN2854324)

Target: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This AGPS antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-AGPS Antibody

Cross-Reactivity: Human

Characteristics: Rabbit Polyclonal antibody to Alkyl-DHAP synthase (alkylglycerone phosphate synthase)
Alkyl-DHAP synthase antibody

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human Alkyl-DHAP synthase. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: human AGPS-transfected 293T cells , MDA-MB-231

Validation: Overexpression

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for AGPS

Target: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Alternative Name: alkylglycerone phosphate synthase

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.

Cellular Localization: Peroxisome membrane

Molecular Weight: 73 kDa

Gene ID: 8540

UniProt: O00116

Pathways: SARS-CoV-2 Protein Interactome