Thiazole Green I Nucleic Acid Gel Stain, 10,000× in DMSO
Select the product you are interested in and add it to your cart:
Catalog Number Size Price Quantity
FLD0601 0.5 mL ¥1600.0
FLD0601-1 1 mL ¥2800.0
Thiazole Green I Nucleic Acid Gel Stain, 10,000× in DMSO | FLD0601 | 0.5 mL
¥1600.0
Thiazole Green I Nucleic Acid Gel Stain, 10,000× in DMSO | FLD0601-1 | 1 mL
¥2800.0
Order on other platforms:
Product Description

Thiazole Green I is a highly sensitive, low-toxicity, and stable green fluorescent dye designed for the detection of double-stranded DNA (dsDNA) in agarose and polyacrylamide gels. Upon binding to dsDNA, it exhibits a marked increase in fluorescence intensity, offering significantly higher sensitivity than traditional ethidium bromide (EtBr) and enabling the detection of low-abundance DNA at the picogram level. With strong affinity for dsDNA and exceptionally low background fluorescence, it delivers high signal-to-noise ratios, facilitating clear band visualization, image analysis, and DNA recovery assessment.

Staining Results

PCR products (1050 bp) stained with GelViewer and imaged using a blue-light transilluminator
DNA molecular weight ladder stained with Thiazole Green I and imaged using a 300 nm UV transilluminator
PCR products (1050 bp) stained with GelViewer and imaged using a blue-light transilluminator
Post-staining of a 1 % agarose gel with Thiazole Green I. Two-fold serial dilutions of λ-DNA/Hind III digest were loaded in amounts of 200, 100, 50, 25, 12.5, 6.25 and 3.125 ng from left to right
Spectral Profile

Excitation and emission spectra of Thiazole Green I nucleic acid gel stain
Excitation and emission spectra of Thiazole Green I nucleic acid gel stain
Related Products

Documents

Troubleshooting

Issue Solution
Smearing or trailing of DNA bands in pre-stained gels 1. Reduce the DNA loading amount to 1/2 or 1/3 of the original. Thiazole Green I is significantly more sensitive than ethidium bromide (EtBr), and overloading may cause overexposure or smearing of bands.
2. Consider switching to post-staining instead of pre-staining. Post-staining minimizes interference with DNA migration and improves imaging quality.
3. For high molecular weight DNA, use a lower percentage agarose gel. Smearing is more common with large DNA fragments.
4. Use TBE buffer instead of TAE. TBE provides stronger buffering capacity and is better suited for high-resolution electrophoresis.
5. Avoid using loading buffers containing SDS, as SDS can disrupt dye–DNA binding and alter migration patterns. If SDS is required, post-staining is strongly recommended for optimal results.
Altered DNA migration in pre-stained gels 1. Reduce the DNA loading amount to 1/2 or 1/3 of the original.
2. Lower the dye concentration; a 0.5× working concentration is recommended for in-gel staining.
3. Use post-staining instead of pre-staining to minimize interference with DNA migration and improve band resolution and imaging quality.
Reduced fluorescence intensity 1. The dye may have precipitated. Warm the solution at 40–50 °C for 1–2 minutes and vortex thoroughly to redissolve.
2. Store the dye at room temperature and protect it from light to prevent precipitation caused by low temperatures.
Copyright © 2025 MSBIO, Inc. All Rights Reserved.

Live Chat