AGPS anticorps (AA 379-658)

N° du produit ABIN6136644

Cet anticorps anti-AGPS est un anticorps Lapin Polyclonal détectant AGPS dans WB. Adapté pour Humain.

Aperçu rapide pour AGPS anticorps (AA 379-658) (ABIN6136644)

Antigène: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AGPS est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-AGPS anticorps

Épitope: AA 379-658

Séquence: IKIRPVPEYQ KYGSVAFPNF EQGVACLREI AKQRCAPASI RLMDNKQFQF GHALKPQVSS IFTSFLDGLK KFYITKFKGF DPNQLSVATL LFEGDREKVL QHEKQVYDIA AKFGGLAAGE DNGQRGYLLT YVIAYIRDLA LEYYVLGESF ETSAPWDRVV DLCRNVKERI TRECKEKGVQ FAPFSTCRVT QTYDAGACIY FYFAFNYRGI SDPLTVFEQT EAAAREEILA NGGSLSHHHG VGKLRKQWLK ESISDVGFGM LKSVKEYVDP NNIFGNRNLL

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 379-658 of human AGPS (NP_003650.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:1000 - 1:2000

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur AGPS

Antigène: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Autre désignation: AGPS

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.,AGPS,ADAP-S,ADAS,ADHAPS,ADPS,ALDHPSY,RCDP3,Neuroscience,AGPS

Poids moléculaire: 72 kDa

ID gène: 8540

UniProt: O00116

Pathways: SARS-CoV-2 Protein Interactome