IDI1 anticorps (AA 31-130)
Aperçu rapide pour IDI1 anticorps (AA 31-130) (ABIN709271)
Antigène
Voir toutes IDI1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
-
-
Épitope
- AA 31-130
-
Fonction
- IDI1 Polyclonal Antibody
-
Réactivité croisée
- Humain, Souris
-
Homologie
- Rat,Cow,Pig,Rabbit
-
Purification
- Purified by Protein A.
-
Immunogène
- KLH conjugated synthetic peptide derived from human IDI1
-
Isotype
- IgG
-
-
-
-
Indications d'application
- WB(1:300-5000),
-
Restrictions
- For Research Use only
-
-
-
Format
- Liquid
-
Concentration
- 1 μg/μL
-
Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
-
Agent conservateur
- ProClin
-
Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Stock
- 4 °C,-20 °C
-
Stockage commentaire
- Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.
-
Date de péremption
- 12 months
-
-
- IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))
-
Autre désignation
- IDI1
-
Sujet
-
Synonyms: IDI1, IPP isomerase 1, IPPI1, Isopentenyl diphosphate Delta isomerase 1, isopentenyl diphosphate dimethylallyl diphosphate isomerase 1, Isopentenyl pyrophosphate isomerase 1, IDI1_HUMAN.
Background: IDI1 is a peroxisomally localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP). These are substrates for the reactions that ultimately result in the synthesis of cholesterol. There is reduction in IPP isomerase activity in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy.
-
ID gène
- 3422
-
UniProt
- Q13907
Antigène
-