FDPS Recombinant Rabbit Monoclonal Antibody (HL2123), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEMA550388-Each-of-1 | In Stock | ₹ 41,385.00 |
FEMA550388 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 41,385.00
GST (18%): ₹ 7,449.30
Total Price: ₹ 48,834.30
Antigen
FDPS
Classification
Recombinant Monoclonal
Concentration
1 mg/mL
Formulation
PBS with no preservative
Gene Accession No.
P05369, P14324, Q920E5
Gene Symbols
FDPS
Immunogen
Recombinant fragment of human FDPS.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Clone
HL2123
Conjugate
Unconjugated
Gene
FDPS
Gene Alias
(2E,6E)-farnesyl diphosphate synthase, 6030492I17Rik, Ac2-125, AI256750, cholesterol-regulated 39 kDa protein, CR 39, dimethylallyltranstransferase, Farnesyl diphosphate synthase, farnesyl diphosphate synthase (farnesyl pyrophosphate synthetase, dimethylallyltranstransferase, geranyltranstransferase), farnesyl diphosphate synthetase, farnesyl pyrophosphate synthase, farnesyl pyrophosphate synthetase, farnesyl pyrophosphate synthetase, dimethylallyltranstransferase, geranyltranstransferase, Fdps, Fdpsl1, FPP synthase, FPP synthetase, FPPS, FPS, geranyltranstransferase, KIAA1293, mKIAA1293, POROK9, testis-specific farnesyl pyrophosphate synthetase
Host Species
Rabbit
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
110196, 2224, 83791
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Isotype
IgG
Related Products
Description
- The isoprene biosynthetic pathway supply the cell with cholesterol, ubiquinone, and various nonsterol metabolites
- The farnesylpyrophosphate synthetase enzyme catalyzes the formation of geranyl and farnesylpyrophosphate from isopentenylpyrophosphate and dimethylallyl pyrophosphate
- Analysis of FDPS activity and protein in rat liver, accompanied by immunofluorescence and immunoelectron microscopy studies, demonstrated that FDPS is predominantly localized in peroxisomes
- 1 Liver tissue from patients with the peroxisomal deficiency diseases Zellweger syndrome and neonatal adrenoleukodystrophy exhibit diminished activities of FDPS and subsequent isoprenoid synthesis.