coding sequence [codon optimized for e. coli k12] Search Results


94
ATCC e coli strain k
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
E Coli Strain K, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Sino Biological human sectm1 / k12 protein
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
Human Sectm1 / K12 Protein, supplied by Sino Biological, 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 coding sequence [codon optimized for e. coli k12]
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
Coding Sequence [Codon Optimized For E. Coli K12], 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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coding sequence [codon optimized for e. coli k12] - by Bioz Stars, 2026-06
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GenScript corporation coding sequence
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
Coding Sequence, 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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coding sequence - by Bioz Stars, 2026-06
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93
Carolina Biological e coli k12
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
E Coli K12, supplied by Carolina Biological, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Addgene inc wild type e coli k12 mg1655
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
Wild Type E Coli K12 Mg1655, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
BASF polyvinylpyrrolidone k 12/25/30/90 (pvp k12/k25/k30/k90)
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
Polyvinylpyrrolidone K 12/25/30/90 (Pvp K12/K25/K30/K90), supplied by BASF, 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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93
Bio-Rad escherichia coli e coli k12 strain hb101
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
Escherichia Coli E Coli K12 Strain Hb101, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
KRUSS GmbH kruss k12 tensiometer
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
Kruss K12 Tensiometer, supplied by KRUSS GmbH, 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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KRUSS GmbH k-12 tensiometer
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
K 12 Tensiometer, supplied by KRUSS GmbH, 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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Promega cdna clone k12
Inhibition of <t>E.</t> <t>coli</t> mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).
Cdna Clone K12, supplied by Promega, 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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Inhibition of E. coli mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).

Journal:

Article Title: Peptide Nucleic Acid Antisense Oligomer as a Therapeutic Strategy against Bacterial Infection: Proof of Principle Using Mouse Intraperitoneal Infection

doi: 10.1128/AAC.49.8.3203-3207.2005

Figure Lengend Snippet: Inhibition of E. coli mutant SM101 growth in vitro by acpP-targeting PNA. PNA was added to cell cultures containing 5 × 105 CFU/ml SM101 to a final concentration of 4, 40, or 400 μM as indicated on the graph, with addition of an equal volume of water as a control (0 μM). Cultures were incubated as described in Materials and Methods. Aliquots of each culture were collected at 2 and 4 h, diluted, and plated for viable cell determination. Error bars indicate standard deviations of the results from three experiments (*, P < 0.01 relative to 2 h control; **, P < 0.001 relative to 4-h control [as determined by Student's t test]).

Article Snippet: E. coli strain K-12 was obtained from the American Type Culture Collection (ATCC 29425) and grown at 37°C in nutrient broth.

Techniques: Inhibition, Mutagenesis, In Vitro, Concentration Assay, Incubation

Inhibition of E. coli wild-type K-12 growth in vitro by acpP-targeting peptide-PNA conjugate. Peptide-PNA conjugate was added to cell cultures containing 5 × 105 CFU/ml E. coli strain K-12 to a final concentration of 0, 4, 40, or 400 μM as indicated on the graph. Cell cultures were grown, and viable cells were determined as described in the legend to Fig. ​Fig.1.1. Error bars indicate standard deviations of the results from two experiments (*, P < 0.001 relative to 2-h control; **, P < 0.005 relative to 4-h control [as determined by Student's t test]).

Journal:

Article Title: Peptide Nucleic Acid Antisense Oligomer as a Therapeutic Strategy against Bacterial Infection: Proof of Principle Using Mouse Intraperitoneal Infection

doi: 10.1128/AAC.49.8.3203-3207.2005

Figure Lengend Snippet: Inhibition of E. coli wild-type K-12 growth in vitro by acpP-targeting peptide-PNA conjugate. Peptide-PNA conjugate was added to cell cultures containing 5 × 105 CFU/ml E. coli strain K-12 to a final concentration of 0, 4, 40, or 400 μM as indicated on the graph. Cell cultures were grown, and viable cells were determined as described in the legend to Fig. ​Fig.1.1. Error bars indicate standard deviations of the results from two experiments (*, P < 0.001 relative to 2-h control; **, P < 0.005 relative to 4-h control [as determined by Student's t test]).

Article Snippet: E. coli strain K-12 was obtained from the American Type Culture Collection (ATCC 29425) and grown at 37°C in nutrient broth.

Techniques: Inhibition, In Vitro, Concentration Assay

Survival of K-12-infected mice due to treatment with acpP-targeting peptide-PNA conjugate. Six-week-old BALB/c mice were i.p. infected with 8 × 108 CFU E. coli strain K-12 in 500 μl PBS (LD90). Infected mice were treated with the peptide-PNA conjugate (100 or 500 nmol) 30 min postinfection; comparisons are made to untreated mice. Survival and general health of these animals was monitored every 6 to 12 h through 9 days.

Journal:

Article Title: Peptide Nucleic Acid Antisense Oligomer as a Therapeutic Strategy against Bacterial Infection: Proof of Principle Using Mouse Intraperitoneal Infection

doi: 10.1128/AAC.49.8.3203-3207.2005

Figure Lengend Snippet: Survival of K-12-infected mice due to treatment with acpP-targeting peptide-PNA conjugate. Six-week-old BALB/c mice were i.p. infected with 8 × 108 CFU E. coli strain K-12 in 500 μl PBS (LD90). Infected mice were treated with the peptide-PNA conjugate (100 or 500 nmol) 30 min postinfection; comparisons are made to untreated mice. Survival and general health of these animals was monitored every 6 to 12 h through 9 days.

Article Snippet: E. coli strain K-12 was obtained from the American Type Culture Collection (ATCC 29425) and grown at 37°C in nutrient broth.

Techniques: Infection

Reduction of  E. coli K-12  bacteremia in mice following treatment with peptide-PNA conjugate a

Journal:

Article Title: Peptide Nucleic Acid Antisense Oligomer as a Therapeutic Strategy against Bacterial Infection: Proof of Principle Using Mouse Intraperitoneal Infection

doi: 10.1128/AAC.49.8.3203-3207.2005

Figure Lengend Snippet: Reduction of E. coli K-12 bacteremia in mice following treatment with peptide-PNA conjugate a

Article Snippet: E. coli strain K-12 was obtained from the American Type Culture Collection (ATCC 29425) and grown at 37°C in nutrient broth.

Techniques: