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Home / Assay Kits / Biochemical Kits

Colorimetric DTT Assay kit

SKU : BHE16300282

This product includes 1 ml of 10x Assay buffer, 0.2 ml of 10 x Reagent A, 0.2 ml of 10 x Reagent B and 0.5 ml of 10x Reagent C.

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Mfr.No.	DTT100C
Description	DTT (Dithiothreitol) is a common reducing agent in biochemistry. Removal of DTT is required for Cys-based protein labeling and for disulfide bond formation in proteins. The Colorimetric DTT Assay Kit (Catalog number DTT100C) is designed for measurement of micromolar concentrations of DTT. The assay is based on measurement of light absorbance at 495 nm. The assay kit can be used for measurements DTT concentrations in biological samples, biochemical reactions and environmental water samples. The assay is compatible with common buffers. It is not compatible with NADH or NADPH. The Colorimetric DTT Assay Kit (catalog number DTT100C) includes 1 ml of 10 x Buffer, 0.2 ml of 10 x Reagent A, 0.2 ml of 10 x Reagent B and 1 ml of 10 x Reagent C. It is for measurement of 100 samples using 96-well plates. Cuvettes may also be used for measurements.
Concentration measurement	Salt and buffer components

Product Manual	Datasheet
Protocols Description	ASSAY PROTOCOL The following assay protocol is based on using a 96-well plate for the measurement. The sample volume is 100 µl and the final assay volume is 190 µl. For 384-well plate assays, the sample volume is 40 µl and the final assay volume is 76 µl. For assays using cuvette, the sample volume is 500 µl and the final assay volume is 950 µl. STANDARD CURVE 1. Sample preparation: Prepare 100 µl of DTT solutions in the wells of a clear 96-well plate with a two-fold serial dilution from 0.1 mM to zero in water or a 20 mM Tris-HCl, pH 8.0 buffer. The 10 x Reagent stock solutions are diluted 10 fold to make the 1 x Reagent solutions. 2. Detection: Add 20 µl of 1x Reagent A and 20 ul of 1 x Reagent B and incubate the mixture for 10 min. The add 50 µl of 1x Reagent C and read the light absorbance at 590 nm (A₅₉₀) 3. Data Analysis: Plot the A₅₉₀ values and the DTT concentration [DTT] to generate the linear standard curve. A₅₉₀ = a [DTT] + b Where the A₅₉₀ values are from experimental data, the a and b values are from the linear fitting between the A₅₉₀ values and the DTT concentrations. UNKNOWN SAMPLES Follow the same procedure to measure the light absorbance at 590 nm (A₅₉₀) values from the unknown samples. Calculate the DTT concentrations in the unknown samples using the A₅₉₀ values from the unknown samples and the a and b values from the standard curve. [DTT] = (A₅₉₀ – b) / a

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SKU	Supplier No.	Size	Your price	Quantity
BHE16300282	DTT100C	100 assays	$277.22		Add to Cart

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