2025-06-03
T4 UvsX Recombinase
RPA001, T4 UvsX Recombinase The T4 UvsX Recombinase is derived from the T4 bacteriophage and is a homolog of the RecA/Rad51 family. It plays an important role in the repair of double stranded DNA breaks and the reactivation of replication forks. T4 UvsX recombinase can combine with
2025-05-27
tinzyme-endonuclease-exonuclease
SspDI (KasI)
RE0585, SspDI (KasI). SspDI belongs to the conventional restriction enzyme series and can recognize G ^ GCGCC sequences. Unlike the Thunder series of rapid endonucleases, SspDI requires a longer time for enzyme cleavage to achieve complete cleavage of the DNA substrate, but this
2025-05-27
tinzyme-endonuclease-exonuclease
BstXI
RE0584, BstXI. BstXI belongs to the Type IIP restriction enzyme and recognizes palindrome sequences. The optimized reaction buffer maximizes the functionality of BstXI, while the reaction buffer contains recombinant albumin, which enhances the stability of various enzymes.
2025-05-27
tinzyme-endonuclease-exonuclease
BspQI
RE0583, BspQI. BspQI belongs to the Type IIS restriction enzyme, which recognizes non palindromic sequences and performs cleavage outside of the recognized sequence. It is commonly used for Golden Gate assembly. The optimized reaction buffer maximizes the functionality
2025-05-27
tinzyme-endonuclease-exonuclease
BsmBI
RE0581, BsmBI BsmBI belongs to the Type IIs restriction enzyme, which can recognize non palindromic sequences and perform cleavage outside of the recognized sequence. It is commonly used for Golden Gate assembly. The optimized reaction buffer maximizes the functionality
2025-05-27
tinzyme-endonuclease-exonuclease
BsiWI
RE0580, BsiWI. BsiWI belongs to the Type IIP restriction enzyme and recognizes palindrome sequences. The optimized reaction buffer maximizes the functionality of BsiWI, while the reaction buffer contains recombinant albumin, which enhances the stability of various enzymes.
2025-05-27
tinzyme-endonuclease-exonuclease
SgeI
RE0579, SgeI. SgeI can cleave DNA targets containing 5-methylcytosine on single or double stranded DNA. SgeI restriction endonuclease can recognize the m5CNNG (9/13) ^ site and has the best cleavage effect at 37°C in its unique buffer. To ensure consistent performance,
2025-05-27
tinzyme-endonuclease-exonuclease
FlashCut™ XhoI
RE0578, FlashCut™ XhoI FlashCut™ Rapid endonucleases are a series of genetically engineered restriction endonucleases that are suitable for rapid enzymatic cleavage of plasmid DNA, PCR products, or genomic DNA. All FlashCut™ Rapid endonucleases have excellent activity in
2025-05-27
RE0577 FlashCut XcmI 480
FlashCut™ XcmI
RE0577, FlashCut™ XcmI. FlashCut™Rapid endonucleases are a series of genetically engineered restriction endonucleases that are suitable for rapid enzymatic cleavage of plasmid DNA, PCR products, or genomic DNA. All FlashCut™ Rapid endonucleases have excellent activity in
2025-05-27
tinzyme-endonuclease-exonuclease
FlashCut™ XbaI
RE0576, FlashCut™ XbaI FlashCut™ Rapid endonucleases are a series of genetically engineered restriction endonucleases that are suitable for rapid enzymatic cleavage of plasmid DNA, PCR products, or genomic DNA. All FlashCut™ Rapid endonucleases have excellent activity in
2025-05-27
tinzyme-endonuclease-exonuclease
FlashCut™ Tsp45I
RE0575, FlashCut™ Tsp45I. FlashCut™ Rapid endonucleases are a series of genetically engineered restriction endonucleases that are suitable for rapid enzymatic cleavage of plasmid DNA, PCR products, or genomic DNA. All FlashCut™ Rapid endonucleases have excellent activity in
2025-05-27
tinzyme-endonuclease-exonuclease
FlashCut™ TaqI
RE0574, FlashCut™ TaqI FlashCut™ Rapid endonucleases are a series of genetically engineered restriction endonucleases that are suitable for rapid enzymatic cleavage of plasmid DNA, PCR products, or genomic DNA. All FlashCut™ Rapid endonucleases have excellent activity in
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