IDI1 antibody (Isopentenyl-Diphosphate delta Isomerase 1) (Center) Primary Antibody
IDI1 Reactivity: Human IHC (p), WB Host: Rabbit Polyclonal
Catalog No. ABIN2856255
Plus shipping costs $45.00
local_shipping Shipping to: United States
Delivery in 3 to 4 Business Days
- Binding Specificity
- This IDI1 antibody is un-conjugated
- Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
- Mouse (Murine), Rat (Rattus), Xenopus laevis, Zebrafish (Danio rerio), Cow (Bovine), Xenopus tropicalis
- Cross-Reactivity (Details)
- Mouse (87 %), Rat (85 %), Xenopus laevis (80 %), Zebrafish (81 %), Bovine (89 %), Xenopus tropicalis (81 %)
- Rabbit polyclonal antibody to IDI1 (isopentenyl-diphosphate delta isomerase 1)
IDI1 antibody [N1C2]
- Purified by antigen-affinity chromatography.
- Recombinant protein encompassing a sequence within the center region of human IDI1. The exact sequence is proprietary.
- Application Notes
- Suggested dilution Reference IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceIHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Western blot1:500-1:3000*
Positive Control: 293T , Molt-4
- For Research Use only
- 0.65 mg/mL
- 0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
- Thimerosal (Merthiolate)
- Precaution of Use
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- -20 °C
- Storage Comment
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
- Alternative Name
- IDI1 (IDI1 Antibody Abstract)
- 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
- Molecular Weight
- 26 kDa
- Gene ID
You are here: