

Add to Cart
FT3
FT3 ELISA TEST KIT
Free Triiodothyronine 96 tests
1. Intended use
Immunoassay for the in vitro quantitative determination of free
triiodothyronine in human serum.
2. Summary
3. Materials provided
• Coated Microplate, 8 x 12 strips, 96 wells, pre-coated with T3
derivant.
• Calibrators, 6 vials, 1 ml each, ready to use; Concentrations:
0(A), 2(B), 5(C), 10(D), 20(E) and 50(F) pmol/L.
• Enzyme Conjugate, 1 vial, 6.0 ml of HRP (horseradish peroxidase)
labeled sheep monoclonal Anti-T3 in Tris-NaCl buffer containing BSA
(bovine serum albumin). Contains 0.2% ProClin300 preservative.
• Substrate, 1 vial, 11ml, ready to use, (tetramethylbenzidine)
TMB.
• Stop Solution, 1 vial, 6.0 ml of 1 mol/l sulfuric acid.
• Wash Solution Concentrate, 1 vial, 25 ml (40X concentrated),
PBS-Tween wash solution.
• IFU, 1 copy.
• Plate Lid: 1 piece.
Materials required (but not provided)
• Microplate reader with 450nm and 620nm wavelength absorbent
capability.
• Microplate washer.
• Incubator.
• Plate shaker.
• Micropipettes and multichannel micropipettes delivering 50μl with
a precision of better than 1.5%.
• Absorbent paper.
• Distilled water.
4. Test Produce
Ensure the patients’ samples, calibrators, and controls are at ambient temperature (18-25 ℃) before measurement. Mix all reagents through gently inverting prior to use.
• Use only the number of wells required and format the microplates’ wells for each calibrator and sample to be assayed. • Add 50 µL of calibrators or samples to each well.
• Add 50 µL of enzyme conjugate to each well.
• Shake the microplate gently for 30 seconds to mix.
• Cover the plate with a plate lid and incubate at 37 ℃ for 60 minutes.
• Discard the contents of the micro plate by decantation or aspiration. If decanting, tap and blot the plate dry with absorbent paper.
• Add 350 µL of wash solution, decant (tap and blot) or aspirate. Repeat 4 additional times for a total of 5 washes. An automated microplate strip washer can be used. At the end of washing, invert the plate and tap out any residual wash solution onto absorbent paper. • Add 100 µL of substrate to each well.
• Cover and incubate at ambient temperature (18-25℃)in the dark for reaction for 20 minutes. Do not shake the plate after substate addition. • Add 50 µL of stop solution to each well.
• Shake for 15-20 seconds to mix the liquid within the wells. It is important to ensure that the blue color changes to yellow completely. • Read the absorbance of each well at 450 nm ( using 620 to 630 nm as the reference wavelength to minimize well imperfections) in a micro plate reader.The results should be read within 30 minutes of adding the stop solution.