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SKU: EG15565S

SacI restriction enzyme recognizes the DNA sequence 5′-GAGCTC-3′ and cleaves to generate cohesive sticky ends. LightNing® SacI is suitable for fast restriction digestion in molecular cloning, plasmid construction, vector preparation, restriction mapping, and analysis of PCR products. A practical option for researchers looking for reliable SacI digestion performance and a cost-effective restriction enzyme for routine molecular biology workflows.

SacI Restriction Enzyme Protocol (PDF)

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€42.00
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SacI Restriction Enzyme for Fast DNA Digestion

SacI restriction enzyme is used for sequence-specific DNA digestion at GAGCTC sites in cloning, plasmid construction, vector preparation and restriction analysis workflows.

  • Product: LightNing® SacI
  • Recognition sequence: 5′-GAGCTC-3′
  • Cleavage pattern: 5’…GAGCT↓C…3′ / 3’…C↑TCGAG…5′
  • Sticky end: 5′ GAGCT overhang
  • Isoschizomers: Psp124BI, SstI
  • Neoschizomers: Ecl136II, EcoICRI, Eco53kI
  • Reaction condition: 1× CutOne® Buffer
  • Incubation temperature: 37°C
  • Digestion time: within 15 minutes
  • Heat inactivation: 80°C for 20 minutes
  • Storage: -20°C
  • Supplied concentration: 20 U/μl
  • Components: LightNing® SacI, 10× CutOne® Buffer, 10× CutOne® Color Buffer

LightNing® enzymes are a series of engineered restriction enzymes that are capable of fast DNA digestion. All LightNing® enzymes show superior activity in the universal CutOne® and CutOne® Color Buffer, and are able to digest DNA in 5~15 minutes. This enables any combination of restriction enzymes to work simultaneously in one reaction tube and eliminates the need for sequential digestions. LightNing® enzymes have passed multiple strict quality controls, and can be used to digest plasmid, genomic and viral DNA as well as PCR products.
CutOne® Color Buffer includes a density reagent along with red and yellow tracking dyes that allow for direct loading of the reaction mixtures on a gel. The red dye of the CutOne® Color Buffer migrates with 2.5 kb double-strand DNA fragments in a 1% agarose gel, and the yellow dye migrates with 10 bp double-strand DNA fragments in a 1% agarose gel.

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