IDI1 anticorps (AA 71-645) (Fluoro594)

N° du produit ABIN8003502

L’anticorps anti-IDI1 Polyclonal Lapin est utilisé pour la détection de IDI1 dans des échantillons de Humain, Souris et Rat. Il a été validé pour FACS.

Aperçu rapide pour IDI1 anticorps (AA 71-645) (Fluoro594) (ABIN8003502)

Antigène: IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp IDI1 est conjugé à/à la Fluoro594

Application: Flow Cytometry (FACS)

Détail du produit anti-IDI1 anticorps (Fluoro594)

Épitope: AA 71-645

Fonction: Anti-IDI1 Antibody Fluoro594 Conjugated

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

Homologie: Human ATG7 shares 92.9% amino acid (aa) sequence identity with both mouse,rat ATG7.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human ATG7 recombinant protein (Position: D71-K645). Human ATG7 shares 92.9% amino acid (aa) sequence identity with both mouse and rat ATG7.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, 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, 0.02 % Sodium azide.

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

Date de péremption: 12 months

Détails sur IDI1

Antigène: IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))

Autre désignation: IDI1

Sujet:

Background: IDI1 encodes a peroxisomally-localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP), which are the substrates for the successive reaction that results in the synthesis of farnesyl diphosphate and, ultimately, cholesterol. It has been shown in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy that there is reduction in IPP isomerase activity.

Gene Full Name: isopentenyl-diphosphate delta isomerase 1

ID gène: 3422

UniProt: Q13907