AASS anticorps (AA 37-865) (HRP)

N° du produit ABIN7968086

L’anticorps anti-AASS Polyclonal Lapin est utilisé pour la détection de AASS dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, ELISA et IHC.

Aperçu rapide pour AASS anticorps (AA 37-865) (HRP) (ABIN7968086)

Antigène: AASS (Aminoadipate Semialdehyde Synthase (AASS))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AASS est conjugé à/à la HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Détail du produit anti-AASS anticorps (HRP)

Épitope: AA 37-865

Fonction: Anti-AASS Antibody HRP Conjugated

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

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human AASS recombinant protein (Position: E37-N865).

Isotype: IgG

Information d'application

Indications d'application: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur AASS

Antigène: AASS (Aminoadipate Semialdehyde Synthase (AASS))

Autre désignation: AASS

Sujet:

Background: Alpha-aminoadipic semialdehyde synthase is an enzyme encoded by the AASS gene in humans and is involved in their major lysine degradation pathway. This gene encodes a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. The N-terminal and the C-terminal portions of this enzyme contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha-aminoadipic semialdehyde. Mutations in this gene are associated with familial hyperlysinemia.

Gene Full Name: aminoadipate-semialdehyde synthase

ID gène: 10157

UniProt: Q9UDR5

Pathways: SARS-CoV-2 Protein Interactome