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pet-28 b (+) vector  (Millipore)


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    Structured Review

    Millipore pet-28 b (+) vector
    Pet 28 B (+) Vector, supplied by Millipore, 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/pet-28(b)+vector/pet28a/pm33247466-61-8-12
    Average 90 stars, based on 1 article reviews
    pet-28 b (+) vector - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.

    Polymerase Chain Reaction:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.

    Amplification:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.

    Clone Assay:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.

    Expressing:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.

    In Vitro:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.

    Protein Purification:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.

    Centrifugation:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.

    Construct:

    Article Title: DNA-Mediated Signaling by Proteins with 4Fe–4S Clusters Is Necessary for Genomic Integrity
    Article Snippet: The dinG gene was amplified from E. coli and was inserted into a pET-28 b (+) vector (Novagen) as described previously.

    Article Title: Regulation of gene expression using chromatin remodelling factors
    Article Snippet: Generation of Deletion Mutants of bnKCP1 The two fragments, bnKCP11-160 and bnKCP11-80, and the entire coding region of bnKCP1 DNA encoding amino acids 1-80, 1-160 and 1-215, respectively, were amplified by PCR and cloned into the HindIII and XhoI sites of pET-28-b vector (Novagen, Madison, Wis.).

    Article Title: Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria.
    Article Snippet: Substrate binding to enzymes often follows a precise order where catalysis is accomplished through programmed conformational changes.. Short-chain dehydrogenase/reductase (SDR) enzymes follow sequential order ‘bi–bi’ reaction kinetics.. The mechanistic study of a SDR homolog, reductase (R) domain, from multifunctional enzymes, e.g. Nonribosomal Peptide Synthetases (NRPSs) and Polyketide Synthases (PKSs) has revealed that it reductively releases 40-phosphopantetheinyl arm-tethered peptidyl product.

    Article Title: Structural insights into the regulation of NADPH binding to reductase domains of nonribosomal peptide synthetases: A concerted loop movement model.
    Article Snippet: The termination module of nonribosomal peptide synthetases (NRPS) and polyketide synthases (PKS) offloads the final product as an acid (occasionally also accompanied by cyclization) upon hydrolysis by employing thioesterase domains (TE-domains).. Reductase domains (R-domains) of short-chain dehydrogenase/reductase (SDR) family offer an alternative offloading mechanism by reducing 4′-phosphopantetheine (4′-PPant) arm-tethered peptidyl chain, a thioester, to an aldehyde or an alcohol.. Recent studies have highlighted their functional importance, for instance in the glycopeptidolipid (GPL) biosynthesis of Mycobacterium smegmatis, where the resulting alcoholic group is the site for subsequent modifications such as glycosylations.

    Article Title: The heterologous expression of a plastocyanin in the diatom Phaeodactylum tricornutum improves cell growth under iron-deficient conditions.
    Article Snippet: The PCR product was then cloned into the pET-28 b (+) vector (Novagen) to obtain the pET-28 b_Fld plasmid for expressing the His-tagged protein in E. coli.

    Article Title: Recombinant expression, purification, and crystallization of the glutaminyl-tRNA synthetase from Toxoplasma gondii.
    Article Snippet: Aminoacyl tRNA synthetases play a critical role in protein synthesis by providing precursor transfer-RNA molecules correctly charged with their cognate amino-acids.. The essential nature of these enzymes make them attractive targets for designing new drugs against important pathogenic protozoans like Toxoplasma.. Because no structural data currently exists for a protozoan glutaminyl-tRNA synthetase (QRS), an understanding of its potential as a drug target and its function in the assembly of the Toxoplasma multi-aminoacyl tRNA (MARS) complex is therefore lacking.

    Article Title: Upstream sequence-dependent suppression and AtxA-dependent activation of protective antigens in Bacillus anthracis
    Article Snippet: To examine the interaction between AtxA and DNA sequences in vitro, the atxA gene was cloned into the expression vector pET 28-b (Novagen, Madison, WI, USA) with N- and C-terminal 6xHIS-tags and an internal FLAG-tag.

    Article Title: Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs
    Article Snippet: The LT-A2/LT-B (referred to as LTA2B) fragment from the plasmid pEnt [ ] was PCR amplified and cloned into an N-terminus His 6 tag containing expression vector, pET-28 b(+) (Novagen, EMD, Gibbstown, NJ), between restriction enzyme sites BamH1 and Sal1 using the following primers: LTA2B-BamH1-F.P: GCC CGT TGC GGA TCC G GGT GAT ACT TGT AAT GAG GAG and LTA2B- Sal1-R.P: GCG AGC CGA GTC GAC GTT TTT CAT ACT GAT TGC CGC.



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