BsaI
Description
Bsal is a type IIS restriction enzyme that recognizes a specific DNA sequence (5′-GGTCTC-3′) and cleaves DNA outside of this recognition site, typically leaving 4-base overhangs.
BsaI’s recognition and cleavage sites are:
5′ GGTCTCN↓ 3′
3′ CCAGAGNNNNN↑ 5′
BsaI is thermostable and can be used in various molecular biology applications, including generation of linear DNA templates for in vitro transcription to synthesize RNA. Type IIS restriction enzymes bind to asymmetric DNA recognition sites but cut the DNA at defined positions located outside of those sites.
The enzyme is provided 20 U/μL in storage buffer. It is also supplied with 1.25 mL of 10X RE Reaction Buffer (500 mM Tris, 1000 mM NaCl, 100 mM MgCl2, 1 mg/mL rHSA, pH 7.9 at 25°C).
Unit definition: The amount of BsaI required to digest 1 µg of pXba DNA in 1 hour at 37°C in a 50 µL reaction.
Product details
Catalog No | E-0099 |
Concentration | 20 U/µL |
Buffer | 10 mM Tris, 300 mM NaCl, 1 mM DTT, 0.1 mM EDTA, 0.5 g/L rHSA, 50% glycerol, pH 7.5 at 25°C |
Volume | 50 µL, 250 µL |
Host | E. coli |
Recommended Storage | -15 to -25°C |
Application | IVT template preparation, restriction digestion |
Product Grade | Molecular Biology |
Shipping Temp | Frozen |
Size | 1,000 U, 5,000 U |
Technical documents
- Safety Data Sheet Look-up open_in_new
- E-0099 Product Insert open_in_new
Product FAQs
ISO 13485 compliant.
Yes
Certificate of analysis
- Certificate of Analysis (CoA) open_in_new
Intellectual property
Products are for research use only, not for use in diagnostic or therapeutic procedures or for use in humans. Products are not for resale without express written permission from TriLink No license under any patent or other intellectual property right of TriLink or its licensors is granted or implied by the purchase unless otherwise provided in writing.
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