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Porcine Fructose-1,6-Bisphosphatase 1 (FBP1) ELISA Kit-Sandwich

Cat. No.EK12F681

Product TypeAnimal Immunoassay Kits

Size

Product Overview

BioVenic Porcine Fructose-1,6-Bisphosphatase 1 (FBP1) ELISA Kit-Sandwich is designed for the quantitative determination of Porcine Fructose-1,6-Bisphosphatase 1 (FBP1) in serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids using a Sandwich ELISA method. For research use only.

Specifications

Assay Type ELISA-Sandwich
Specificity The assay kit is specific for Porcine FBP1.
Target Species Swine
Species Reactivity Swine
Reproducibility Intra-Assay: CV < 10%; Inter-Assay: CV < 10%
Assay Time Around 270 min
Sample Requirement Serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids.

Target Information

Fructose-1,6-Bisphosphatase 1 is encoded by the FBP1 gene in pigs. FBP1 is a key enzyme in the evolutionary conserved pathway of gluconeogenesis. It is the only distinct gluconeogenic enzyme in the upper part of the gluconeogenic pathway through which the flux of this pathway can be regulated. The fold of fructose-1,6-bisphosphatase from pigs is identical to that of inositol-1-phosphatase (IMPase).

Target/Biomarker Porcine FBP1
Target Synonym Fructose-1, 6-bisphosphatase 1; FBPase 1; D-fructose-1, 6-bisphosphate 1-phosphohydrolase 1; FBP1; FBP; 3.1.3.11
Gene ID 397038
UniProt ID P00636

Shipping and Storage

This product is shipped with gel ice packs. It is recommended to store at 2-8 °C (Up to 6 months).

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

  1. Ghanem, A. et al. Mutational analysis of fructose-1,6-bis-phosphatase FBP1 indicates partially independent functions in gluconeogenesis and sensitivity to genotoxic stress. Microbial cell (Graz, Austria). 2017, 4: 52-63.
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