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Thermo Scientific FastDigest BseJI restriction enzyme recognizes the GATNN^NNATC site and oxidizes in 5–15 minutes at 65°C using universal FastDigest buffer. Best cutting results. Iso-cleavage enzymes: BsaBI, Bse8I.

Thermo Scientific FastDigest BseJI is one of a series of high-end fast restriction enzymes that are 100% active in both Universal FastDigest Buffer and FastDigest Green Reaction Buffer.

Universal buffer can quickly complete DNA single, double or multiple enzyme digestion in 5–15 minutes without the need for buffer changes or subsequent DNA purification steps. For a table of enzymatic activities, heat inactivation, and incubation times for this and other FastDigest restriction enzymes, see Reaction conditions for FastDigest enzyme< /a>. DNA modifying enzymes (such as Klenow fragment, T4 DNA Ligase, alkaline phosphatase and T4 DNA Polymerase) are 100% active in FastDigest buffer. Therefore, enzymes used in downstream applications can be added directly to the FastDigest reaction mixture.

For convenience, FastDigest Green Buffer includes 1 density reagent and 2 tracking dyes for loading digestion reaction products directly onto the gel.

Shorter incubation times and optimized universal FastDigest buffer composition eliminate star activity effects.

Features

•100% activity of all FastDigest enzymes in universal buffers
•100% buffer compatibility with downstream applications
• Complete digestion in 5–15 minutes
• Load directly onto gel
• No star activity
• 176 FastDigest enzymes available

Applications< /b>

•Molecular cloning
•Restriction site mapping
•Genotyping
•Southern blot
•Restriction fragment length polymorphism (RFLP)
• SNP Analysis

Remarks: FastDigest Green Buffer has the same high performance as colorless FastDigest Buffer in DNA digestion reactions and downstream applications. For applications requiring product analysis by fluorescence excitation (eg determination of concentration under UV light), the use of colorless FastDigest buffer is recommended.

See product specifications for information on methylation sensitivity.