zrai (New England Biolabs)
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New England Biolabs manufactures this product 
92
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Name:
ZraI
Description:
ZraI 1 000 units
Catalog Number:
r0659l
Price:
269
Category:
Restriction Enzymes
Size:
1 000 units
|
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Structured Review
New England Biolabs
zrai
ZraI 1 000 units
https://www.bioz.com/result/zrai/product/New England Biolabs
Average 92 stars, based on 1 article reviews
Price from $9.99 to $1999.99
ZraI 1 000 units
https://www.bioz.com/result/zrai/product/New England Biolabs
Average 92 stars, based on 1 article reviews
Price from $9.99 to $1999.99
zrai - by Bioz Stars,
2021-03
92/100 stars
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Related Articles
Introduce:Article Title: Small secreted proteins enable biofilm development in the cyanobacterium Synechococcus elongatus Article Snippet: .. Vectors used to introduce the WT and mutated complementation DNA fragments into NS1 were generated using the GeneArt® Seamless Cloning and Assembly Kit (Life Technologies) on PCR-generated cloning fragments and standardized devices (a chloramphenicol resistance device and a NS1 device with tetracycline resistance) derived via Generated:Article Title: Small secreted proteins enable biofilm development in the cyanobacterium Synechococcus elongatus Article Snippet: .. Vectors used to introduce the WT and mutated complementation DNA fragments into NS1 were generated using the GeneArt® Seamless Cloning and Assembly Kit (Life Technologies) on PCR-generated cloning fragments and standardized devices (a chloramphenicol resistance device and a NS1 device with tetracycline resistance) derived via Clone Assay:Article Title: Small secreted proteins enable biofilm development in the cyanobacterium Synechococcus elongatus Article Snippet: .. Vectors used to introduce the WT and mutated complementation DNA fragments into NS1 were generated using the GeneArt® Seamless Cloning and Assembly Kit (Life Technologies) on PCR-generated cloning fragments and standardized devices (a chloramphenicol resistance device and a NS1 device with tetracycline resistance) derived via Polymerase Chain Reaction:Article Title: Small secreted proteins enable biofilm development in the cyanobacterium Synechococcus elongatus Article Snippet: .. Vectors used to introduce the WT and mutated complementation DNA fragments into NS1 were generated using the GeneArt® Seamless Cloning and Assembly Kit (Life Technologies) on PCR-generated cloning fragments and standardized devices (a chloramphenicol resistance device and a NS1 device with tetracycline resistance) derived via Derivative Assay:Article Title: Small secreted proteins enable biofilm development in the cyanobacterium Synechococcus elongatus Article Snippet: .. Vectors used to introduce the WT and mutated complementation DNA fragments into NS1 were generated using the GeneArt® Seamless Cloning and Assembly Kit (Life Technologies) on PCR-generated cloning fragments and standardized devices (a chloramphenicol resistance device and a NS1 device with tetracycline resistance) derived via Expressing:Article Title: Variation in Mutation Spectra Among CRISPR/Cas9 Mutagenized Poplars Article Snippet: Next, the promoter, sgRNA, and terminator cassettes (with one or two sgRNAs) in the modified AtU6-26SK vectors and the 35S-Cas9-SK vector were digested with HindIII (NEB) and ligated together using T4 ligase (NEB). .. Then, the plant expression vector pK2GW7 was digested with KpnI-HF (NEB) and Article Title: Variation in Mutation Spectra Among CRISPR/Cas9 Mutagenized Poplars Article Snippet: Then, the plant expression vector pK2GW7 was digested with KpnI-HF (NEB) and ZraI (NEB). .. The entire piece containing the sgRNA expression cassette(s) and the Cas9 expression cassette in the modified 35S-Cas9-SK vector was digested with KpnI-HF (NEB) and SmaI (NEB) and ligated into the KpnI and Plasmid Preparation:Article Title: Variation in Mutation Spectra Among CRISPR/Cas9 Mutagenized Poplars Article Snippet: Next, the promoter, sgRNA, and terminator cassettes (with one or two sgRNAs) in the modified AtU6-26SK vectors and the 35S-Cas9-SK vector were digested with HindIII (NEB) and ligated together using T4 ligase (NEB). .. Then, the plant expression vector pK2GW7 was digested with KpnI-HF (NEB) and Article Title: Variation in Mutation Spectra Among CRISPR/Cas9 Mutagenized Poplars Article Snippet: The entire piece containing the sgRNA expression cassette(s) and the Cas9 expression cassette in the modified 35S-Cas9-SK vector was digested with KpnI-HF (NEB) and SmaI (NEB) and ligated into the KpnI and ZraI sites in the already digested pK2GW7 using T4 ligase (NEB). .. For the empty-vector control construct, the Cas9 cassette was digested using KpnI-HF (NEB) and SmaI (NEB) from the 35S-Cas9-SK vector and ligated into the pK2GW7 already digested with KpnI and Article Title: Genetic Transformation of a C. trachomatis Ocular Isolate With the Functional Tryptophan Synthase Operon Confers an Indole-Rescuable Phenotype Article Snippet: The 2.7 Kb trpRBA operon was isolated by gel extraction using the Wizard® SV Gel and PCR Clean-Up System (Promega). .. The pCDS5KO shuttle vector (Wang et al., ) was digested with Article Title: Variation in Mutation Spectra Among CRISPR/Cas9 Mutagenized Poplars Article Snippet: Then, the plant expression vector pK2GW7 was digested with KpnI-HF (NEB) and ZraI (NEB). .. The entire piece containing the sgRNA expression cassette(s) and the Cas9 expression cassette in the modified 35S-Cas9-SK vector was digested with KpnI-HF (NEB) and SmaI (NEB) and ligated into the KpnI and Construct:Article Title: Variation in Mutation Spectra Among CRISPR/Cas9 Mutagenized Poplars Article Snippet: The entire piece containing the sgRNA expression cassette(s) and the Cas9 expression cassette in the modified 35S-Cas9-SK vector was digested with KpnI-HF (NEB) and SmaI (NEB) and ligated into the KpnI and ZraI sites in the already digested pK2GW7 using T4 ligase (NEB). .. For the empty-vector control construct, the Cas9 cassette was digested using KpnI-HF (NEB) and SmaI (NEB) from the 35S-Cas9-SK vector and ligated into the pK2GW7 already digested with KpnI and Modification:Article Title: Variation in Mutation Spectra Among CRISPR/Cas9 Mutagenized Poplars Article Snippet: Then, the plant expression vector pK2GW7 was digested with KpnI-HF (NEB) and ZraI (NEB). .. The entire piece containing the sgRNA expression cassette(s) and the Cas9 expression cassette in the modified 35S-Cas9-SK vector was digested with KpnI-HF (NEB) and SmaI (NEB) and ligated into the KpnI and |