Nucleic Acid

G-Biosciences&rsquo FastPure&trade Spin Columns (Mini and Midi) are designed for easy and efficient small scale protein purification. These versatile spin columns are made of biocompatible polypropylene and are compatible with all chromatography

G-Biosciences&rsquo FastPure&trade Spin Columns (Mini and Midi) are designed for easy and efficient small scale protein purification. These versatile spin columns are made of biocompatible polypropylene and are compatible with all chromatography

G-Biosciences&rsquo FastPure&trade Spin Columns (Mini and Midi) are designed for easy and efficient small scale protein purification. These versatile spin columns are made of biocompatible polypropylene and are compatible with all chromatography

G-Biosciences&rsquo FastPure&trade Spin Columns (Mini and Midi) are designed for easy and efficient small scale protein purification. These versatile spin columns are made of biocompatible polypropylene and are compatible with all chromatography

The Bio Basic Inc. deionized formamide is suitable for laboratory and research use. Application: For Laboratory Research Only

For nucleic acid hybridization and sequencing.

For nucleic acid hybridization and sequencing.

Gel and PCR Extraction System (100 preps): The Gel and PCR Extraction System provides a simple and efficient method for extraction of DNA from agarose gels, and purification of DNA from enzymatic reactions such as PCR or restriction enzyme

Gel and PCR Extraction System (100 preps): The Gel and PCR Extraction System provides a simple and efficient method for extraction of DNA from agarose gels, and purification of DNA from enzymatic reactions such as PCR or restriction enzyme

Gel Extraction Kit (100 preps): Bio Basic Gel Extraction Kit is an excellent tool offering a rapid and economic method to extract DNA from an agarose gel. This technology is based on binding DNA to silica-based membrane, followed by subsequent wash

Gel Extraction Kit (100 preps): Bio Basic Gel Extraction Kit is an excellent tool offering a rapid and economic method to extract DNA from an agarose gel. This technology is based on binding DNA to silica-based membrane, followed by subsequent wash

These preparations contain genomic DNA extracted from defined microorganisms at low passage. The DNA starting material was analysed with standardised methods to determine the DNA&rsquos integrity and quantity.