IDI1 anticorps

N° du produit ABIN2856255

Cet anticorps anti-IDI1 est un anticorps Lapin Polyclonal détectant IDI1 dans WB et IHC (p). Adapté pour Humain.

Aperçu rapide pour IDI1 anticorps (ABIN2856255)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp IDI1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-IDI1 anticorps

Réactivité croisée: Humain

Attributs du produit: Rabbit polyclonal antibody to IDI1 (isopentenyl-diphosphate delta isomerase 1)
IDI1 antibody [N1C2]

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human IDI1. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: Molt-4

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.65 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur IDI1

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

Autre désignation: isopentenyl-diphosphate delta isomerase 1

Sujet: 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.

Cellular Localization: Peroxisome

Poids moléculaire: 26 kDa

ID gène: 3422

UniProt: Q13907