e coli jm109 cells (TaKaRa)
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e coli jm109 cells
E Coli Jm109 Cells, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 345 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/e+coli+jm109/Monoclonal+Anti-mouse+P-cadherin/pm41518045-21-13-17
Average 95 stars, based on 345 article reviews
E Coli Jm109 Cells, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 345 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/e+coli+jm109/Monoclonal+Anti-mouse+P-cadherin/pm41518045-21-13-17
Average 95 stars, based on 345 article reviews
e coli jm109 cells - by Bioz Stars,
2026-09
95/100 stars
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Construct:Article Title: From phenotype to receptor: validating physiological clustering of Escherichia coli phages through comprehensive receptor analysis. Article Snippet: .. The resulting constructs were initially transformed into Article Title: Engineering of acyl ligase domain in non-ribosomal peptide synthetases to change fatty acid moieties of lipopeptides Article Snippet: .. Second, we constructed a pUC19-based plasmid (pUC19-mycU-erm-PrplGB-fenF-ituAL-mycACP-mycAD) using an In-Fusion® HD Cloning Kit (New England Biolabs, Ipswich, MA, USA) and Article Title: Engineering of acyl ligase domain in NRPS to design fatty acid moieties of lipopeptides Article Snippet: .. 616 Second, we constructed a pUC19-based plasmid (pUC19-mycU-erm-PrplGB-fenF-ituAL-617 mycACP-mycAD) using an In-Fusion® HD Cloning Kit (New England Biolabs, Ipswich, MA, 618 USA) and Article Title: Method for enzymatically producing maytansinol Article Snippet: .. Mutant enzyme library fragments were amplified by inverse PCR using primers FpnbA_A107X and RpnbA_A107X (SEQ ID NOS: 7 and 8) and pCDF-capA-bspnbA as the template, cyclized by using T4 kinase (Toyobo) and Ligation high (Toyobo), and used to transform Transformation Assay:Article Title: From phenotype to receptor: validating physiological clustering of Escherichia coli phages through comprehensive receptor analysis. Article Snippet: .. The resulting constructs were initially transformed into Plasmid Preparation:Article Title: Engineering of acyl ligase domain in non-ribosomal peptide synthetases to change fatty acid moieties of lipopeptides Article Snippet: .. Second, we constructed a pUC19-based plasmid (pUC19-mycU-erm-PrplGB-fenF-ituAL-mycACP-mycAD) using an In-Fusion® HD Cloning Kit (New England Biolabs, Ipswich, MA, USA) and Article Title: Engineering of acyl ligase domain in NRPS to design fatty acid moieties of lipopeptides Article Snippet: .. 616 Second, we constructed a pUC19-based plasmid (pUC19-mycU-erm-PrplGB-fenF-ituAL-617 mycACP-mycAD) using an In-Fusion® HD Cloning Kit (New England Biolabs, Ipswich, MA, 618 USA) and Cloning:Article Title: Engineering of acyl ligase domain in non-ribosomal peptide synthetases to change fatty acid moieties of lipopeptides Article Snippet: .. Second, we constructed a pUC19-based plasmid (pUC19-mycU-erm-PrplGB-fenF-ituAL-mycACP-mycAD) using an In-Fusion® HD Cloning Kit (New England Biolabs, Ipswich, MA, USA) and Article Title: Engineering of acyl ligase domain in NRPS to design fatty acid moieties of lipopeptides Article Snippet: .. 616 Second, we constructed a pUC19-based plasmid (pUC19-mycU-erm-PrplGB-fenF-ituAL-617 mycACP-mycAD) using an In-Fusion® HD Cloning Kit (New England Biolabs, Ipswich, MA, 618 USA) and Control:Article Title: Biosynthesis of High Toughness Poly(3‐Hydroxypropionate)‐Based Block Copolymers With Poly(D‐2‐Hydroxybutyrate) and Poly(D‐Lactate) Segments Using Evolved Monomer Sequence‐Regulating Polyester Synthase Article Snippet: .. Article Title: Biosynthesis of High Toughness Poly(3-Hydroxypropionate)-Based Block Copolymers With Poly(D-2-Hydroxybutyrate) and Poly(D-Lactate) Segments Using Evolved Monomer Sequence-Regulating Polyester Synthase. Article Snippet: This study synthesized poly(3hydroxypropionate) [P(3HP)]containing polyhydroxyalkanoate (PHA) block copolymers, P(3HP)bP[2hydroxybutyrate (2HB)] and P(3HP)bP(Dlactate) (PDLA), using Escherichia coli.. The cells expressing an evolved sequenceregulating PHA synthase, PhaCARNDFH, and propionylCoA transferase were cultured with the supplementation of the corresponding monomer precursors in the medium.. The block structure of P(3HP)bPDLA was confirmed by proton nuclear magnetic resonance analysis and solvent fractionation. Mutagenesis:Article Title: Biosynthesis of High Toughness Poly(3‐Hydroxypropionate)‐Based Block Copolymers With Poly(D‐2‐Hydroxybutyrate) and Poly(D‐Lactate) Segments Using Evolved Monomer Sequence‐Regulating Polyester Synthase Article Snippet: .. Article Title: Biosynthesis of High Toughness Poly(3-Hydroxypropionate)-Based Block Copolymers With Poly(D-2-Hydroxybutyrate) and Poly(D-Lactate) Segments Using Evolved Monomer Sequence-Regulating Polyester Synthase. Article Snippet: This study synthesized poly(3hydroxypropionate) [P(3HP)]containing polyhydroxyalkanoate (PHA) block copolymers, P(3HP)bP[2hydroxybutyrate (2HB)] and P(3HP)bP(Dlactate) (PDLA), using Escherichia coli.. The cells expressing an evolved sequenceregulating PHA synthase, PhaCARNDFH, and propionylCoA transferase were cultured with the supplementation of the corresponding monomer precursors in the medium.. The block structure of P(3HP)bPDLA was confirmed by proton nuclear magnetic resonance analysis and solvent fractionation. Article Title: Method for enzymatically producing maytansinol Article Snippet: .. Mutant enzyme library fragments were amplified by inverse PCR using primers FpnbA_A107X and RpnbA_A107X (SEQ ID NOS: 7 and 8) and pCDF-capA-bspnbA as the template, cyclized by using T4 kinase (Toyobo) and Ligation high (Toyobo), and used to transform Amplification:Article Title: Method for enzymatically producing maytansinol Article Snippet: .. Mutant enzyme library fragments were amplified by inverse PCR using primers FpnbA_A107X and RpnbA_A107X (SEQ ID NOS: 7 and 8) and pCDF-capA-bspnbA as the template, cyclized by using T4 kinase (Toyobo) and Ligation high (Toyobo), and used to transform Inverse PCR:Article Title: Method for enzymatically producing maytansinol Article Snippet: .. Mutant enzyme library fragments were amplified by inverse PCR using primers FpnbA_A107X and RpnbA_A107X (SEQ ID NOS: 7 and 8) and pCDF-capA-bspnbA as the template, cyclized by using T4 kinase (Toyobo) and Ligation high (Toyobo), and used to transform Ligation:Article Title: Method for enzymatically producing maytansinol Article Snippet: .. Mutant enzyme library fragments were amplified by inverse PCR using primers FpnbA_A107X and RpnbA_A107X (SEQ ID NOS: 7 and 8) and pCDF-capA-bspnbA as the template, cyclized by using T4 kinase (Toyobo) and Ligation high (Toyobo), and used to transform Article Title: Optogenetic control of Corynebacterium glutamicum gene expression. Article Snippet: .. The 10 μL ligation system was used to transform competent cells of Bacteria:Article Title: Method for enzymatically producing maytansinol Article Snippet: .. Mutant enzyme library fragments were amplified by inverse PCR using primers FpnbA_A107X and RpnbA_A107X (SEQ ID NOS: 7 and 8) and pCDF-capA-bspnbA as the template, cyclized by using T4 kinase (Toyobo) and Ligation high (Toyobo), and used to transform Incubation:Article Title: Method for enzymatically producing maytansinol Article Snippet: .. Mutant enzyme library fragments were amplified by inverse PCR using primers FpnbA_A107X and RpnbA_A107X (SEQ ID NOS: 7 and 8) and pCDF-capA-bspnbA as the template, cyclized by using T4 kinase (Toyobo) and Ligation high (Toyobo), and used to transform |
