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Manufacturer: Finetest

This kit is based on Double antibody-Sandwich ELISA detection method and takes 4h assay time. The microplate provided in this kit has been precoated with anti TNFSF11/RANKL antibody. Read the O.D. absorbance at 450nm in a microplate reader. Calculate the concentration of TNFSF11/RANKL in the sample by plotting standard curve. The concentration of the target substance is proportional to the OD450 value.

Manufacturer: Finetest

This kit is based on Double antibody-Sandwich ELISA detection method and takes 4h assay time. The microplate provided in this kit has been precoated with anti PTGS2/COX-2 antibody. Read the O.D. absorbance at 450nm in a microplate reader. Calculate the concentration of PTGS2/COX-2 in the sample by plotting standard curve. The concentration of the target substance is proportional to the OD450 value.

Manufacturer: Finetest

This kit is based on Double antibody-Sandwich ELISA detection method and takes 4h assay time. The microplate provided in this kit has been precoated with anti FETUA antibody. Read the O.D. absorbance at 450nm in a microplate reader. Calculate the concentration of FETUA in the sample by plotting standard curve. The concentration of the target substance is proportional to the OD450 value.

Manufacturer: Finetest

The Rat PRL (Prolactin) ELISA Kit from FineTest is designed for the quantitative measurement of prolactin levels in rat serum, plasma, and other biological fluids. This assay utilizes the sandwich ELISA principle, employing specific antibodies to detect prolactin with high sensitivity and specificity. The kit includes pre-coated 96-well plates, standards, detection reagents, and all necessary components for the assay. It offers a user-friendly protocol with an assay time of approximately 3 hours. The detection range typically spans from 15.6 pg/mL to 1000 pg/mL, with a sensitivity of less than 9.4 pg/mL. This kit is suitable for research applications involving prolactin-related studies in rats.

Manufacturer: Finetest

This kit is based on Double antibody-Sandwich ELISA detection method and takes 4h assay time. The microplate provided in this kit has been precoated with anti COL2 antibody. Read the O.D. absorbance at 450nm in a microplate reader. Calculate the concentration of COL2 in the sample by plotting standard curve. The concentration of the target substance is proportional to the OD450 value.

Manufacturer: Finetest

This kit is based on Double antibody-Sandwich ELISA detection method and takes 4h assay time. The microplate provided in this kit has been precoated with anti TIMP-1 antibody. Read the O.D. absorbance at 450nm in a microplate reader. Calculate the concentration of TIMP-1 in the sample by plotting standard curve. The concentration of the target substance is proportional to the OD450 value.

Manufacturer: Finetest

This kit is based on Competitive-ELISA detection method and takes 2h assay time. The microplate provided in this kit has been precoated with COR. COR in the sample or standard competes with a fixed amount of biotin-labeled COR for sites on a pre-coated antibody specific to COR. Read the O.D. absorbance at 450nm in a microplate reader. Compare OD450 value of sample with the standard curve through curve fitting software to determine the concentration of COR in the sample. The concentration of the target substance is inversely proportional to the OD450 value.

Manufacturer: Finetest

This kit is based on Double antibody-Sandwich ELISA detection method and takes 4h assay time. The microplate provided in this kit has been precoated with anti Hspa5 antibody. Add standard and properly diluted sample into relevant well respectively. Read the O.D. absorbance at 450nm in a microplate reader. Calculate the concentration of Hspa5 in the sample by plotting standard curve. The concentration of the target substance is proportional to the OD450 value.

Manufacturer: Finetest

This kit is based on Double antibody-Sandwich ELISA detection method and takes 4h assay time. The microplate provided in this kit has been precoated with anti KL antibody. Add standard and properly diluted sample into relevant well respectively. Read the O.D. absorbance at 450nm in a microplate reader. Calculate the concentration of KL in the sample by plotting standard curve. The concentration of the target substance is proportional to the OD450 value.