The CpoI (RsrII) restriction enzyme recognizes CG^GWCCG sites and cuts best at 37°C in Tango buffer (Isoschizomers: CspI, Rsr2I, RsrII).

Safely eliminate DNA contamination from RNA samples

Ideal tool for clearing residual DNA

CAS: 9001-62-1

Optimize electrophoresis of both genomic and large supercoiled DNA in agarose and polyacrylamide gels with Thermo Scientific™ 50X TAE Buffer (Tris-acetate-EDTA).

Catalyze the removal of 5'- and 3'-phosphate groups from DNA, RNA, nucleotides, and proteins using this thermosensitive alkaline phosphatase .

Cut GAAGAC(2/6)^ sites with BpiI (BbsI) restriction enzyme, which performs best at 37°C in G buffer (Isoschizomers: BbsI, BpuAI, BstV2I).

Cut at GG^CGCGCC sites with Thermo Scientific™ FastDigest™ AscI (SgsI), which performs best at 37°C in 5-15 minutes using universal FastDigest Buffer (Isoschizomers: PalAI).

CORNING™ Supersome™ Human UGT2B10, 0.5 mL is prepared from insect cells infected with baculovirus containing human UGT2B10 cDNA

For PCR amplification of long strand and GC-rich DNA templates, cloning and cDNA amplification applications

Perform single-, double- or multiple DNA digestion within 5-15 minutes with this advanced line of restriction enzymes, 100% active in one universal buffer.

Enzymes and buffer in single mix

Perform single-, double- or multiple DNA digestion within 5-15 minutes withthis advanced line of restriction enzymes, 100% active in one universal buffer.

The FastDigest EcoRI restriction enzyme recognizes G^AATTC sites and cuts best at 37°C in 5-15 minutes using universal FastDigest Buffer.

Cut at Gm6A^TC sites with Thermo Scientific™ FastDigest™ DpnI, which performs best at 37°C in 5-15 minutes using universal FastDigest Buffer (Isoschizomers: MalI).

Cut at G^GTACC sites with Acc65I (Asp718I) restriction enzyme, which performs best at 37°C in O buffer (Isoschizomers: Asp718I).

Catalyzes the formation of phosphodiester bonds in the presence of ATP between double-stranded DNAs with 3' hydroxyl and 5' phosphate termini

Perform single-, double- or multiple DNA digestion within 5-15 minutes withthis advanced line of restriction enzymes, 100% active in one universal buffer.

Purified from bovine pancreas

Used as carrier for nucleic acid precipitation in ethanol

The PstI restriction enzyme recognizes CTGCA^G sites and cuts best at 37°C in O buffer (Isoschizomers: BspMAI).

RNase T1 is an endoribonuclease that specifically degrades single-stranded RNA at G residues.

Proteinase K highly active and stable endopeptidase used in wide range of applications purified from fungus T. album.

Degrade single-stranded DNA and RNA with this endonuclease.

Perform single-, double- or multiple DNA digestion within 5-15 minutes with this advanced line of restriction enzymes, 100% active in one universal buffer.

Perform single-, double- or multiple DNA digestion within 5-15 minutes withthis advanced line of restriction enzymes, 100% active in one universal buffer.

Catalyze the hydrolysis of inorganic pyrophosphate to two orthophosphates.

T4 DNA Ligase catalyzes the formation of a phosphodiester bond between juxtaposed 5'-phosphate and 3'-hydroxyl termini in duplex DNA or RNA.

Cut at CC^SGG sites with BcnI (NciI) restriction enzyme, which performs best at 37°C in Tango buffer (Isoschizomers: AsuC2I, BpuMI, NciI).