e coli reference gene Search Results


90
ATCC e coli strain atcc pta
E Coli Strain Atcc Pta, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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91
ATCC e coli strain atcc
E Coli Strain Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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e coli strain atcc - by Bioz Stars, 2026-09
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Genlantis inc e. coli cytosine deaminase (cd) gene
E. Coli Cytosine Deaminase (Cd) Gene, supplied by Genlantis inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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e. coli cytosine deaminase (cd) gene - by Bioz Stars, 2026-09
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Gene Bridges Inc quick & easy e. coli gene deletion kit
Quick & Easy E. Coli Gene Deletion Kit, supplied by Gene Bridges Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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quick & easy e. coli gene deletion kit - by Bioz Stars, 2026-09
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90
GenScript corporation gene encoding e. coli lpla
Gene Encoding E. Coli Lpla, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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gene encoding e. coli lpla - by Bioz Stars, 2026-09
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Celtek Bioscience LLC e. coli codon-optimized wild-type caspase-6 gene with a 6xhis at c-terminus
E. Coli Codon Optimized Wild Type Caspase 6 Gene With A 6xhis At C Terminus, supplied by Celtek Bioscience LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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e. coli codon-optimized wild-type caspase-6 gene with a 6xhis at c-terminus - by Bioz Stars, 2026-09
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GenScript corporation e. coli codon-optimized gene encoding prpta ii 1
E. Coli Codon Optimized Gene Encoding Prpta Ii 1, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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e. coli codon-optimized gene encoding prpta ii 1 - by Bioz Stars, 2026-09
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90
Gene Bridges Inc e. coli shuffle® express host cell
E. Coli Shuffle® Express Host Cell, supplied by Gene Bridges Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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e. coli shuffle® express host cell - by Bioz Stars, 2026-09
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Gene Bridges Inc e. coli t7e2 cells
E. Coli T7e2 Cells, supplied by Gene Bridges Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GenScript corporation e. coli thioesterase gene tesa
a Schematic illustration of FFA production pathway. The truncated acyl-CoA <t>thioesterase</t> gene (‘ <t>tesA</t> ), under control of P clac143 inducible promoter, was inserted into the chromosome with simultaneous knockout of the endogenous long-chain-fatty-acid--CoA ligase ( fadD ). ‘TesA converts fatty acyl-ACP to free fatty acid and its reconversion to fatty acyl-CoA is negated by knocking out the endogenous fadD . Comparison of the growth and FFA productivity of the engineered Synechococcus sp. PCC 11901 and PCC 7002 strains using regular AD7 ( b ) and MAD ( c ) medium. Filled and dashed lines indicate growth (OD 730 measurements) of the induced and non-induced cultures respectively, while the column bars correspond to the FFA production. Arrows indicate addition of IPTG inducer and light intensity increase. d Comparison of growth and FFA production by the WT (dashed lines and columns) and Δ fadD knockout control (filled lines and columns) strains. e Analysis of FFA production by the engineered PCC 11901 strain induced at OD 730 ≈ 8. FFA were extracted either directly from the culture or from the medium supernatant. For OD 730 measurements data points with error bars represent mean of n = 3 biological replicates ±standard deviation (for PCC 11901 Δ fadD :: tesA strain n = 2 in panels b and c and n = 3 in panel e ). FFA concentration as mean of n = 6 replicates (three biological and two technical) ±standard deviation (for 11901 Δ fadD :: tesA strain n = 4 in panels b and c and n = 6 in panel e ). f Detail of WT and engineered PCC 11901 strain cultures centrifuged after 7 days of cultivation. g Lipidomic profiles of the FFA from PCC 11901 and PCC 7002 FFA producer strains: C12:0 (lauric acid), C14:0 (myristic acid), C16:0 (palmitic acid), C18:0 (stearic acid) and C18:1n9t (elaidic acid).
E. Coli Thioesterase Gene Tesa, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/e+coli+reference+gene/e++coli+thioesterase+gene+tesa/pmc07205611-264-5-23
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e. coli thioesterase gene tesa - by Bioz Stars, 2026-09
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90
Sigma-Genosys panorama e. coli gene arrays
a Schematic illustration of FFA production pathway. The truncated acyl-CoA <t>thioesterase</t> gene (‘ <t>tesA</t> ), under control of P clac143 inducible promoter, was inserted into the chromosome with simultaneous knockout of the endogenous long-chain-fatty-acid--CoA ligase ( fadD ). ‘TesA converts fatty acyl-ACP to free fatty acid and its reconversion to fatty acyl-CoA is negated by knocking out the endogenous fadD . Comparison of the growth and FFA productivity of the engineered Synechococcus sp. PCC 11901 and PCC 7002 strains using regular AD7 ( b ) and MAD ( c ) medium. Filled and dashed lines indicate growth (OD 730 measurements) of the induced and non-induced cultures respectively, while the column bars correspond to the FFA production. Arrows indicate addition of IPTG inducer and light intensity increase. d Comparison of growth and FFA production by the WT (dashed lines and columns) and Δ fadD knockout control (filled lines and columns) strains. e Analysis of FFA production by the engineered PCC 11901 strain induced at OD 730 ≈ 8. FFA were extracted either directly from the culture or from the medium supernatant. For OD 730 measurements data points with error bars represent mean of n = 3 biological replicates ±standard deviation (for PCC 11901 Δ fadD :: tesA strain n = 2 in panels b and c and n = 3 in panel e ). FFA concentration as mean of n = 6 replicates (three biological and two technical) ±standard deviation (for 11901 Δ fadD :: tesA strain n = 4 in panels b and c and n = 6 in panel e ). f Detail of WT and engineered PCC 11901 strain cultures centrifuged after 7 days of cultivation. g Lipidomic profiles of the FFA from PCC 11901 and PCC 7002 FFA producer strains: C12:0 (lauric acid), C14:0 (myristic acid), C16:0 (palmitic acid), C18:0 (stearic acid) and C18:1n9t (elaidic acid).
Panorama E. Coli Gene Arrays, supplied by Sigma-Genosys, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/e+coli+reference+gene/panorama+e++coli+gene+arrays/10__1128_slash_jb__186__16__5432___5441__2004-73-24-29
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panorama e. coli gene arrays - by Bioz Stars, 2026-09
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90
Synbio Technologies LLC gene cloning and expression in e. coli genes
a Schematic illustration of FFA production pathway. The truncated acyl-CoA <t>thioesterase</t> gene (‘ <t>tesA</t> ), under control of P clac143 inducible promoter, was inserted into the chromosome with simultaneous knockout of the endogenous long-chain-fatty-acid--CoA ligase ( fadD ). ‘TesA converts fatty acyl-ACP to free fatty acid and its reconversion to fatty acyl-CoA is negated by knocking out the endogenous fadD . Comparison of the growth and FFA productivity of the engineered Synechococcus sp. PCC 11901 and PCC 7002 strains using regular AD7 ( b ) and MAD ( c ) medium. Filled and dashed lines indicate growth (OD 730 measurements) of the induced and non-induced cultures respectively, while the column bars correspond to the FFA production. Arrows indicate addition of IPTG inducer and light intensity increase. d Comparison of growth and FFA production by the WT (dashed lines and columns) and Δ fadD knockout control (filled lines and columns) strains. e Analysis of FFA production by the engineered PCC 11901 strain induced at OD 730 ≈ 8. FFA were extracted either directly from the culture or from the medium supernatant. For OD 730 measurements data points with error bars represent mean of n = 3 biological replicates ±standard deviation (for PCC 11901 Δ fadD :: tesA strain n = 2 in panels b and c and n = 3 in panel e ). FFA concentration as mean of n = 6 replicates (three biological and two technical) ±standard deviation (for 11901 Δ fadD :: tesA strain n = 4 in panels b and c and n = 6 in panel e ). f Detail of WT and engineered PCC 11901 strain cultures centrifuged after 7 days of cultivation. g Lipidomic profiles of the FFA from PCC 11901 and PCC 7002 FFA producer strains: C12:0 (lauric acid), C14:0 (myristic acid), C16:0 (palmitic acid), C18:0 (stearic acid) and C18:1n9t (elaidic acid).
Gene Cloning And Expression In E. Coli Genes, supplied by Synbio Technologies LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/e+coli+reference+gene/gene+cloning+and+expression+in+e++coli+genes/10__3389_slash_fenrg__2021__680313-129-0-15
Average 90 stars, based on 1 article reviews
gene cloning and expression in e. coli genes - by Bioz Stars, 2026-09
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Image Search Results


a Schematic illustration of FFA production pathway. The truncated acyl-CoA thioesterase gene (‘ tesA ), under control of P clac143 inducible promoter, was inserted into the chromosome with simultaneous knockout of the endogenous long-chain-fatty-acid--CoA ligase ( fadD ). ‘TesA converts fatty acyl-ACP to free fatty acid and its reconversion to fatty acyl-CoA is negated by knocking out the endogenous fadD . Comparison of the growth and FFA productivity of the engineered Synechococcus sp. PCC 11901 and PCC 7002 strains using regular AD7 ( b ) and MAD ( c ) medium. Filled and dashed lines indicate growth (OD 730 measurements) of the induced and non-induced cultures respectively, while the column bars correspond to the FFA production. Arrows indicate addition of IPTG inducer and light intensity increase. d Comparison of growth and FFA production by the WT (dashed lines and columns) and Δ fadD knockout control (filled lines and columns) strains. e Analysis of FFA production by the engineered PCC 11901 strain induced at OD 730 ≈ 8. FFA were extracted either directly from the culture or from the medium supernatant. For OD 730 measurements data points with error bars represent mean of n = 3 biological replicates ±standard deviation (for PCC 11901 Δ fadD :: tesA strain n = 2 in panels b and c and n = 3 in panel e ). FFA concentration as mean of n = 6 replicates (three biological and two technical) ±standard deviation (for 11901 Δ fadD :: tesA strain n = 4 in panels b and c and n = 6 in panel e ). f Detail of WT and engineered PCC 11901 strain cultures centrifuged after 7 days of cultivation. g Lipidomic profiles of the FFA from PCC 11901 and PCC 7002 FFA producer strains: C12:0 (lauric acid), C14:0 (myristic acid), C16:0 (palmitic acid), C18:0 (stearic acid) and C18:1n9t (elaidic acid).

Journal: Communications Biology

Article Title: Newly discovered Synechococcus sp. PCC 11901 is a robust cyanobacterial strain for high biomass production

doi: 10.1038/s42003-020-0910-8

Figure Lengend Snippet: a Schematic illustration of FFA production pathway. The truncated acyl-CoA thioesterase gene (‘ tesA ), under control of P clac143 inducible promoter, was inserted into the chromosome with simultaneous knockout of the endogenous long-chain-fatty-acid--CoA ligase ( fadD ). ‘TesA converts fatty acyl-ACP to free fatty acid and its reconversion to fatty acyl-CoA is negated by knocking out the endogenous fadD . Comparison of the growth and FFA productivity of the engineered Synechococcus sp. PCC 11901 and PCC 7002 strains using regular AD7 ( b ) and MAD ( c ) medium. Filled and dashed lines indicate growth (OD 730 measurements) of the induced and non-induced cultures respectively, while the column bars correspond to the FFA production. Arrows indicate addition of IPTG inducer and light intensity increase. d Comparison of growth and FFA production by the WT (dashed lines and columns) and Δ fadD knockout control (filled lines and columns) strains. e Analysis of FFA production by the engineered PCC 11901 strain induced at OD 730 ≈ 8. FFA were extracted either directly from the culture or from the medium supernatant. For OD 730 measurements data points with error bars represent mean of n = 3 biological replicates ±standard deviation (for PCC 11901 Δ fadD :: tesA strain n = 2 in panels b and c and n = 3 in panel e ). FFA concentration as mean of n = 6 replicates (three biological and two technical) ±standard deviation (for 11901 Δ fadD :: tesA strain n = 4 in panels b and c and n = 6 in panel e ). f Detail of WT and engineered PCC 11901 strain cultures centrifuged after 7 days of cultivation. g Lipidomic profiles of the FFA from PCC 11901 and PCC 7002 FFA producer strains: C12:0 (lauric acid), C14:0 (myristic acid), C16:0 (palmitic acid), C18:0 (stearic acid) and C18:1n9t (elaidic acid).

Article Snippet: A synthetic version of the E. coli thioesterase gene tesA lacking its cognate signal sequence ( ‘tesA ) was codon-optimised for Syn7002 (by GenScript, Hong Kong, Ltd). pAcsA_cpt_YFP and pAcsA_cLac143_YFP vector templates for PCR were a kind gift from Prof. Brian Pfleger, University of Wisconsin-Madison, USA and pDF-trc was a kind gift from Prof. Patrik Jones, Imperial College London, UK.

Techniques: Control, Knock-Out, Comparison, Standard Deviation, Concentration Assay

FFA production yields achieved by engineered photoautotrophic and heterotrophic hosts having similar modifications.

Journal: Communications Biology

Article Title: Newly discovered Synechococcus sp. PCC 11901 is a robust cyanobacterial strain for high biomass production

doi: 10.1038/s42003-020-0910-8

Figure Lengend Snippet: FFA production yields achieved by engineered photoautotrophic and heterotrophic hosts having similar modifications.

Article Snippet: A synthetic version of the E. coli thioesterase gene tesA lacking its cognate signal sequence ( ‘tesA ) was codon-optimised for Syn7002 (by GenScript, Hong Kong, Ltd). pAcsA_cpt_YFP and pAcsA_cLac143_YFP vector templates for PCR were a kind gift from Prof. Brian Pfleger, University of Wisconsin-Madison, USA and pDF-trc was a kind gift from Prof. Patrik Jones, Imperial College London, UK.

Techniques: Modification