ptwin1 vector (New England Biolabs)
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93
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New England Biolabs
ptwin1 vector
Ptwin1 Vector, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 93/100, based on 218 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ptwin1/pTWIN1+Vector+DNA/pmc12032424-132-25-27
Average 93 stars, based on 218 article reviews
Ptwin1 Vector, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 93/100, based on 218 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ptwin1/pTWIN1+Vector+DNA/pmc12032424-132-25-27
Average 93 stars, based on 218 article reviews
ptwin1 vector - by Bioz Stars,
2026-09
93/100 stars
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Related Articles
Plasmid Preparation:Article Title: Influence of RNA structural stability on the RNA chaperone activity of the Escherichia coli protein StpA Article Snippet: .. The plasmid used for cloning and purification of StpA and the respective mutant was Article Title: High-Yield Soluble Expression and Simple Purification of the Antimicrobial Peptide OG2 Using the Intein System in Escherichia coli Article Snippet: .. The two codon-optimized OG2 genes including C-OG2 (C-terminal fusion expression) gene and N-OG2 (N-terminal fusion expression) gene were amplified using splitting overlap extension (SOE) PCR and cloned into the Cloning:Article Title: Influence of RNA structural stability on the RNA chaperone activity of the Escherichia coli protein StpA Article Snippet: .. The plasmid used for cloning and purification of StpA and the respective mutant was Purification:Article Title: Influence of RNA structural stability on the RNA chaperone activity of the Escherichia coli protein StpA Article Snippet: .. The plasmid used for cloning and purification of StpA and the respective mutant was Mutagenesis:Article Title: Influence of RNA structural stability on the RNA chaperone activity of the Escherichia coli protein StpA Article Snippet: .. The plasmid used for cloning and purification of StpA and the respective mutant was Polymerase Chain Reaction:Article Title: Synthesis of L-nucleic acids by means of an enzyme Article Snippet: .. PCR product 2 was made using Article Title: Synthesis of L-nucleic acids by means of an enzyme Article Snippet: .. PCR product 2 was made using Article Title: Adenosine Triphosphate Stimulates Aquifex aeolicus MutL Endonuclease Activity Article Snippet: The forward and reverse primers incorporated NdeI and SapI restriction sites, respectively, for subcloning into the pTWIN1 vector (New England Biolabs, Inc.). .. The PCR product was digested with NdeI and SapI restriction endonucleases (New England Biolabs, Inc) and subcloned into the same sites in Expressing:Article Title: High-Yield Soluble Expression and Simple Purification of the Antimicrobial Peptide OG2 Using the Intein System in Escherichia coli Article Snippet: .. The two codon-optimized OG2 genes including C-OG2 (C-terminal fusion expression) gene and N-OG2 (N-terminal fusion expression) gene were amplified using splitting overlap extension (SOE) PCR and cloned into the Amplification:Article Title: High-Yield Soluble Expression and Simple Purification of the Antimicrobial Peptide OG2 Using the Intein System in Escherichia coli Article Snippet: .. The two codon-optimized OG2 genes including C-OG2 (C-terminal fusion expression) gene and N-OG2 (N-terminal fusion expression) gene were amplified using splitting overlap extension (SOE) PCR and cloned into the Overlap Extension Polymerase Chain Reaction:Article Title: High-Yield Soluble Expression and Simple Purification of the Antimicrobial Peptide OG2 Using the Intein System in Escherichia coli Article Snippet: .. The two codon-optimized OG2 genes including C-OG2 (C-terminal fusion expression) gene and N-OG2 (N-terminal fusion expression) gene were amplified using splitting overlap extension (SOE) PCR and cloned into the Clone Assay:Article Title: High-Yield Soluble Expression and Simple Purification of the Antimicrobial Peptide OG2 Using the Intein System in Escherichia coli Article Snippet: .. The two codon-optimized OG2 genes including C-OG2 (C-terminal fusion expression) gene and N-OG2 (N-terminal fusion expression) gene were amplified using splitting overlap extension (SOE) PCR and cloned into the other:Article Title: Regulation of hierarchical carbon substrate utilization, nitrogen fixation, and root colonization by the Hfq/Crc/CrcZY genes in Pseudomonas stutzeri Article Snippet: pTWIN1 , |