AGPS Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2714463

Détail du produit

Antigène: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette AGPS protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human AGPS / AAG5 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

Antigène: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Autre désignation: Agps,aag5 (AGPS Produits)

Synonymes: fd16e06 Protein, zgc:56718 Protein, wu:fd16e06 Protein, ADAP-S Protein, ADAS Protein, ADHAPS Protein, ADPS Protein, ALDHPSY Protein, 5832437L22 Protein, 9930035G10Rik Protein, AW123847 Protein, Adaps Protein, Adas Protein, Adhaps Protein, Adps Protein, Aldhpsy Protein, bs2 Protein, Adap-s Protein, Ads Protein, alkylglycerone phosphate synthase Protein, alkylglycerone phosphate synthase L homeolog Protein, agps Protein, AGPS Protein, agps.L Protein, Agps Protein

Sujet: 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.

Poids moléculaire: 67 kDa

NCBI Accession: NP_003650

Pathways: SARS-CoV-2 Protein Interactome