■ Silica-membrane technology ensures fast and ready-to-use high-quality DNA. ■ High DNA yield, excellent repeatability. ■ This kit significantly removes contaminants and inhibitors, facilitating downstream applications
■ Excellent compatibility that fulfils the needs of purification of DNA fragments from both gels and solutions. ■ Stable process plus pH indicator allow the easy determination of the optimal pH for DNA binding.
■ High-quality virus RNA can be obtained within one hour. ■ No phenol / chloroform extraction and ethanol precipitation. ■ High RNA yield and excellent repeatability. ■ Complete removal of contaminants and inhibitors, facilitating downstream applications.
■ Optimized buffers for plant samples make the process more convenience. ■ Unique DNase I minimizes genomic DNA contamination. ■ Unique filtration column CS eliminates other contaminations. ■ High-purity ready-to-use RNA, suited for sensitive downstream
■ Optimized buffers and protocols for cultured cells and bacteria samples make the process simple and convenient. ■ Unique DNase I minimizes genomic DNA contamination. ■ Unique RNase-free Filtration Columns CS eliminates other contaminations.
■ Optimized buffers for animal tissue samples make the process simple and convenient. ■ Unique DNase I minimizes genomic DNA contamination. ■ Higher-purity ready-to-use RNA, suitable for sensitive downstream applications. ■ No phenol / chloroform extracti
Isolate pure DNA from all soil samples and difficult sample types, such as flower bed soil, potting soil, farmland soil, forest soil, sludge, red soil, black soil, dust and many other kinds of soil samples. The whole experimental procedure could be finish
■ Silica membrane technology ensures simple and rapid purification of highquality DNA from swab. ■ The purified DNA from swabs is ready-to-use in downstream applications. ■ 0.5 - 3.5 μg genomic DNA can be isolated from one swab sample.
■ Rapid purification of high-quality DNA. ■ No phenol / chloroform extraction is required. ■ Carrier RNA enhances binding of micro DNA to spin column membrane. ■ Complete removal of contaminants and inhibitors, facilitating downstream applications.
■ High quality virus DNA/RNA can be purified from samples of various virus including HBV, HPV, HCV and enteroviruses within one hour. ■ No phenol/chloroform extraction. ■ High yield, excellent repeatability and totally free from contaminants and inhibitor
■ Specially developed for marine animal samples. ■ No phenol / chloroform extraction. ■ High-quality purified DNA can be obtained in 1 to 2 hours. The high pure genomic DNA can be used directly in downstream applications.
■ The procedure is fast, convenient, and can be finished within one hour. ■ No phenol/chloroform extraction. ■ 3-30 μg genomic DNA can be purified from 100 mg plant samples. ■ OD260/OD280 value is within the range of 1.7 - 1.9.
■ High efficiency: Blend of DNA polymerases allow for automatic “hot-start” ■ High Fidelity: especially for high-specificity, high-fidelity DNA amplification