Nicking Endonuclease Nb.BsrDI (Recognition Site: 5'-GCAATGNN-3', Bottom-Strand Nicking)
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Nicking Endonuclease Nb.BsrDI (Recognition Site: 5'-GCAATGNN-3', Bottom-Strand Nicking)

Cat.No: IVDRM-0163 Datasheet

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Product Name Nicking Endonuclease Nb.BsrDI (Recognition Site: 5'-GCAATGNN-3', Bottom-Strand Nicking)
Catalog No. IVDRM-0163
Description Nb.BsrDI is a nicking endonuclease that recognizes the sequence 5'-GCAATGNN-3' and cleaves only one strand (the bottom strand) of a double-stranded DNA substrate, generating a single-stranded nick without cutting the duplex through. With an optimal reaction temperature of 65°C, this enzyme is well suited for workflows that benefit from elevated incubation temperatures.
Intended Use For molecular cloning applications requiring site-specific nicking of double-stranded DNA.
Principle / Technology Nicking endonuclease: cleaves only one strand of the dsDNA substrate. Nb.BsrDI nicks the bottom strand two nucleotides downstream of its recognition site (3'-CGTTAC↑NN-5'), producing a nick rather than a double-strand break.
Sample Type Double-stranded DNA (dsDNA) substrates.
Performance Range / Specifications Concentration: 10 U/µL.
One unit (U) is the amount of enzyme required to completely convert 1 µg of supercoiled pUC19 DNA to the open circular form in 1 hour at 65°C in a 50 µL reaction.
Specificity Recognizes 5'-GCAATGNN-3' and nicks the bottom strand. Methylation effect: none.
Reaction Conditions / Protocol 1× reaction buffer; incubate at 65°C.
Heat inactivation: 80°C for 20 min.
Components / Formulation Nb.BsrDI nicking endonuclease, 10 U/µL; supplied with the recommended reaction buffer.
Storage Conditions Store at -25°C to -15°C.
Shelf Life 2 years when stored at -25°C to -15°C.
Package Specifications 2000 U
Concentration 10 U/µL
Activity / Unit Definition One unit (U) is defined as the amount of enzyme required to completely convert 1 µg of supercoiled pUC19 DNA into the open circular form within 1 hour at 65°C in a 50 µL reaction.
Expiration Date / Stability Stable for 2 years at -25°C to -15°C.
Recommended Buffer System 1× universal restriction enzyme reaction buffer (supplied).
Application Notes / Precautions Incubate reactions at 65°C for optimal activity.
Cleavage is not affected by common DNA methylation.
Inactivate the enzyme at 80°C for 20 min before downstream steps.
Avoid repeated freeze-thaw cycles; store at -25°C to -15°C.
Recognition Site 5'-GCAATGNN-3'
3'-CGTTAC↑NN-5'
(Nb.BsrDI cleaves the bottom strand, as indicated by ↑.)
Heat Inactivation 80°C for 20 min.
Methylation Sensitivity Not affected by methylation.

For research use only, not for clinical use.

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