AGPS anticorps (AA 154-658)

N° du produit ABIN7600146

L’anticorps anti-AGPS Polyclonal Lapin est utilisé pour la détection de AGPS dans des échantillons de Humain. Il a été validé pour WB, ELISA, IHC, FACS, ICC et IF.

Aperçu rapide pour AGPS anticorps (AA 154-658) (ABIN7600146)

Antigène: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AGPS est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunocytochemistry (ICC), Immunofluorescence (IF)

Détail du produit anti-AGPS anticorps

Épitope: AA 154-658

Fonction: Anti-AGPS Antibody

Réactivité croisée (Details): No cross-reactivity with other proteins.

Attributs du produit: Anti-AGPS Antibody. Tested in ELISA, Flow Cytometry, IF, IHC, ICC, WB applications. This antibody reacts with Human.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human AGPS recombinant protein (Position: D154-L658).

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.1-0.25 μg/mL, Human Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x10^6 cells, Human ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur AGPS

Antigène: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Autre désignation: AGPS

Sujet:

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.

Gene Full Name: alkylglycerone phosphate synthase

Poids moléculaire: 73 kDa

ID gène: 8540

UniProt: O00116

Pathways: SARS-CoV-2 Protein Interactome