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pet30a expression vector  (New England Biolabs)


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    New England Biolabs pet30a expression vector
    Pet30a Expression Vector, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 4837 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pet30a+expression+vector/NdeI/pmc11125983-59-46-53
    Average 99 stars, based on 4837 article reviews
    pet30a expression vector - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Amplification:

    Article Title: Development of a Gold Nanoparticle Vaccine against Enterohemorrhagic Escherichia coli O157:H7
    Article Snippet: EHEC (EDL933) DNA was isolated via the use of a Qiagen DNeasy blood and tissue kit, following the manufacturer’s directions. .. Sequences encoding LomW (GenBank protein accession no. 12514345) and EscC (GenBank protein accession no. 12518466) were amplified via the use of Phusion polymerase (New England BioLabs) and cloned into a pET30a( ) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Article Title: Development of a Gold Nanoparticle Vaccine against Enterohemorrhagic Escherichia coli O157:H7
    Article Snippet: EHEC (EDL933) DNA was isolated via the use of a Qiagen DNeasy blood and tissue kit, following the manufacturer’s directions. .. Sequences encoding LomW (GenBank protein accession no. 12514345 ) and EscC (GenBank protein accession no. 12518466 ) were amplified via the use of Phusion polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Article Title: Use of Reverse Vaccinology in the Design and Construction of Nanoglycoconjugate Vaccines against Burkholderia pseudomallei
    Article Snippet: 321 322 Cloning and Expression of Burkholderia Antigens 323 B. mallei ATCC 23344 DNA was isolated via QIAGEN® DNeasy® Blood and Tissue Kit, 324 according to manufacturer’s directions. .. Sequences encoding OmpW (BMA2010/ BPSL2704), 325 Porin OpcP1 (BMAA1122/BPSS0708), Hemagglutinin (BMAA1324/BPSS0908), Hcp1 326 (BMAA0742/BPSS1498), FlgD (BMA3327/BPSL0272), OpcP porin (BMAA1353/ BPSS0879), 327 porin (BMAA0599/BPSS0757) and FlgL (BMA3336/BPSL0281) were amplified via Phusion® 328 polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI 329 and XhoI or HindIII-HF® (New England BioLabs) restriction sites (Table S2). ..

    Article Title: Optimization of Multivalent Gold Nanoparticle Vaccines Eliciting Humoral and Cellular Immunity in an In Vivo Model of Enterohemorrhagic Escherichia coli O157:H7 Colonization
    Article Snippet: EHEC (EDL933) genomic DNA was isolated via a Qiagen DNeasy blood and tissue kit according to the manufacturer’s directions. .. Sequences encoding LomW (GI:12514345), EscC (GI:12518466), LpfA1 (GI:12518278), and LpfA2 (GI:12518581) were amplified via Phusion polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Clone Assay:

    Article Title: Development of a Gold Nanoparticle Vaccine against Enterohemorrhagic Escherichia coli O157:H7
    Article Snippet: EHEC (EDL933) DNA was isolated via the use of a Qiagen DNeasy blood and tissue kit, following the manufacturer’s directions. .. Sequences encoding LomW (GenBank protein accession no. 12514345) and EscC (GenBank protein accession no. 12518466) were amplified via the use of Phusion polymerase (New England BioLabs) and cloned into a pET30a( ) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Article Title: Development of a Gold Nanoparticle Vaccine against Enterohemorrhagic Escherichia coli O157:H7
    Article Snippet: EHEC (EDL933) DNA was isolated via the use of a Qiagen DNeasy blood and tissue kit, following the manufacturer’s directions. .. Sequences encoding LomW (GenBank protein accession no. 12514345 ) and EscC (GenBank protein accession no. 12518466 ) were amplified via the use of Phusion polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Article Title: Use of Reverse Vaccinology in the Design and Construction of Nanoglycoconjugate Vaccines against Burkholderia pseudomallei
    Article Snippet: 321 322 Cloning and Expression of Burkholderia Antigens 323 B. mallei ATCC 23344 DNA was isolated via QIAGEN® DNeasy® Blood and Tissue Kit, 324 according to manufacturer’s directions. .. Sequences encoding OmpW (BMA2010/ BPSL2704), 325 Porin OpcP1 (BMAA1122/BPSS0708), Hemagglutinin (BMAA1324/BPSS0908), Hcp1 326 (BMAA0742/BPSS1498), FlgD (BMA3327/BPSL0272), OpcP porin (BMAA1353/ BPSS0879), 327 porin (BMAA0599/BPSS0757) and FlgL (BMA3336/BPSL0281) were amplified via Phusion® 328 polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI 329 and XhoI or HindIII-HF® (New England BioLabs) restriction sites (Table S2). ..

    Article Title: Efficacy of EHEC gold nanoparticle vaccines evaluated with the Shiga toxin-producing Citrobacter rodentium mouse model.
    Article Snippet: EHEC (EDL933) DNA was isolated with a DNeasy Blood and Tissue Kit (Qiagen), following the manufacturer’s directions. .. To improve recombinant protein solubility, the N-termi nus signal sequences of EscC (GenBank protein accession no. 12518466) and LomW (GenBank protein accession no. 12514345) were predicted using the SignalP 6.0 server, and the DNA segments without the predicted signal sequences were cloned into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs) restriction sites. ..

    Article Title: Optimization of Multivalent Gold Nanoparticle Vaccines Eliciting Humoral and Cellular Immunity in an In Vivo Model of Enterohemorrhagic Escherichia coli O157:H7 Colonization
    Article Snippet: EHEC (EDL933) genomic DNA was isolated via a Qiagen DNeasy blood and tissue kit according to the manufacturer’s directions. .. Sequences encoding LomW (GI:12514345), EscC (GI:12518466), LpfA1 (GI:12518278), and LpfA2 (GI:12518581) were amplified via Phusion polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Article Title: Efficacy of EHEC gold nanoparticle vaccines evaluated with the Shiga toxin-producing Citrobacter rodentium mouse model
    Article Snippet: EHEC (EDL933) DNA was isolated with a DNeasy Blood and Tissue Kit (Qiagen), following the manufacturer’s directions. .. To improve recombinant protein solubility, the N-terminus signal sequences of EscC (GenBank protein accession no. 12518466) and LomW (GenBank protein accession no. 12514345) were predicted using the SignalP 6.0 server, and the DNA segments without the predicted signal sequences were cloned into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs) restriction sites. ..

    Expressing:

    Article Title: Development of a Gold Nanoparticle Vaccine against Enterohemorrhagic Escherichia coli O157:H7
    Article Snippet: EHEC (EDL933) DNA was isolated via the use of a Qiagen DNeasy blood and tissue kit, following the manufacturer’s directions. .. Sequences encoding LomW (GenBank protein accession no. 12514345) and EscC (GenBank protein accession no. 12518466) were amplified via the use of Phusion polymerase (New England BioLabs) and cloned into a pET30a( ) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Article Title: Development of a Gold Nanoparticle Vaccine against Enterohemorrhagic Escherichia coli O157:H7
    Article Snippet: EHEC (EDL933) DNA was isolated via the use of a Qiagen DNeasy blood and tissue kit, following the manufacturer’s directions. .. Sequences encoding LomW (GenBank protein accession no. 12514345 ) and EscC (GenBank protein accession no. 12518466 ) were amplified via the use of Phusion polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Article Title: Use of Reverse Vaccinology in the Design and Construction of Nanoglycoconjugate Vaccines against Burkholderia pseudomallei
    Article Snippet: 321 322 Cloning and Expression of Burkholderia Antigens 323 B. mallei ATCC 23344 DNA was isolated via QIAGEN® DNeasy® Blood and Tissue Kit, 324 according to manufacturer’s directions. .. Sequences encoding OmpW (BMA2010/ BPSL2704), 325 Porin OpcP1 (BMAA1122/BPSS0708), Hemagglutinin (BMAA1324/BPSS0908), Hcp1 326 (BMAA0742/BPSS1498), FlgD (BMA3327/BPSL0272), OpcP porin (BMAA1353/ BPSS0879), 327 porin (BMAA0599/BPSS0757) and FlgL (BMA3336/BPSL0281) were amplified via Phusion® 328 polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI 329 and XhoI or HindIII-HF® (New England BioLabs) restriction sites (Table S2). ..

    Article Title: Efficacy of EHEC gold nanoparticle vaccines evaluated with the Shiga toxin-producing Citrobacter rodentium mouse model.
    Article Snippet: EHEC (EDL933) DNA was isolated with a DNeasy Blood and Tissue Kit (Qiagen), following the manufacturer’s directions. .. To improve recombinant protein solubility, the N-termi nus signal sequences of EscC (GenBank protein accession no. 12518466) and LomW (GenBank protein accession no. 12514345) were predicted using the SignalP 6.0 server, and the DNA segments without the predicted signal sequences were cloned into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs) restriction sites. ..

    Article Title: Further Evaluation of Enterohemorrhagic Escherichia coli Gold Nanoparticle Vaccines Utilizing Citrobacter rodentium as the Model Organism
    Article Snippet: Briefly, DNA from EHEC strain EDL933 was extracted with a DNeasy Blood and Tissue kit (Qiagen, Germantown, MD, USA), according to the manufacturer’s instructions. .. To enhance solubility of recombinant EscC (GenBank protein accession no. 12518466), the N-terminal signal sequence of the protein was predicted using the SignalP 6.0 program, and the DNA segment without the predicted signal sequence was inserted in-frame with an ^X His-tag at the C-terminus into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs, Ipswich, MA, USA). ..

    Article Title: Crystal Structure of H227A Mutant of Arginine Kinase in Daphnia magna Suggests the Importance of Its Stability
    Article Snippet: These PCR products, containing mutated gene, was extracted by QIAquick Gel Extraction Kit (Hilden, Germany, QIAGEN) and utilized to second PCR step as primer with primer Dm AK-NdeI-F (Forward) and Dm AK-NotI-R, which didn’t use at first PCR. .. The mutated genes, after second PCR, were inserted into the pET30a expression vector (Ipswich, MA, USA, New England Biolabs) using a restriction enzyme of Nde I and Not I (Kusatsu, Japan, Takara). .. The recombinant plasmids of Dm AK histidine mutants (H90A, H227A, H284A and H315A) were induced to express in BL21(DE3) Escherichia coli ( E. coli ) system with 0.5 mM isopropyl β-D-1-thiogalactopyranoside (IPTG) (Haarlem, Netherlands, Duchefa Biochemie) for overnight at 20 °C and 170 rpm.

    Article Title: Optimization of Multivalent Gold Nanoparticle Vaccines Eliciting Humoral and Cellular Immunity in an In Vivo Model of Enterohemorrhagic Escherichia coli O157:H7 Colonization
    Article Snippet: EHEC (EDL933) genomic DNA was isolated via a Qiagen DNeasy blood and tissue kit according to the manufacturer’s directions. .. Sequences encoding LomW (GI:12514345), EscC (GI:12518466), LpfA1 (GI:12518278), and LpfA2 (GI:12518581) were amplified via Phusion polymerase (New England BioLabs) and cloned into a pET30a(+) expression vector using NdeI and XhoI or HindIII-HF (New England BioLabs) restriction sites. ..

    Article Title: Efficacy of EHEC gold nanoparticle vaccines evaluated with the Shiga toxin-producing Citrobacter rodentium mouse model
    Article Snippet: EHEC (EDL933) DNA was isolated with a DNeasy Blood and Tissue Kit (Qiagen), following the manufacturer’s directions. .. To improve recombinant protein solubility, the N-terminus signal sequences of EscC (GenBank protein accession no. 12518466) and LomW (GenBank protein accession no. 12514345) were predicted using the SignalP 6.0 server, and the DNA segments without the predicted signal sequences were cloned into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs) restriction sites. ..

    Recombinant:

    Article Title: Efficacy of EHEC gold nanoparticle vaccines evaluated with the Shiga toxin-producing Citrobacter rodentium mouse model.
    Article Snippet: EHEC (EDL933) DNA was isolated with a DNeasy Blood and Tissue Kit (Qiagen), following the manufacturer’s directions. .. To improve recombinant protein solubility, the N-termi nus signal sequences of EscC (GenBank protein accession no. 12518466) and LomW (GenBank protein accession no. 12514345) were predicted using the SignalP 6.0 server, and the DNA segments without the predicted signal sequences were cloned into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs) restriction sites. ..

    Article Title: Further Evaluation of Enterohemorrhagic Escherichia coli Gold Nanoparticle Vaccines Utilizing Citrobacter rodentium as the Model Organism
    Article Snippet: Briefly, DNA from EHEC strain EDL933 was extracted with a DNeasy Blood and Tissue kit (Qiagen, Germantown, MD, USA), according to the manufacturer’s instructions. .. To enhance solubility of recombinant EscC (GenBank protein accession no. 12518466), the N-terminal signal sequence of the protein was predicted using the SignalP 6.0 program, and the DNA segment without the predicted signal sequence was inserted in-frame with an ^X His-tag at the C-terminus into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs, Ipswich, MA, USA). ..

    Article Title: Efficacy of EHEC gold nanoparticle vaccines evaluated with the Shiga toxin-producing Citrobacter rodentium mouse model
    Article Snippet: EHEC (EDL933) DNA was isolated with a DNeasy Blood and Tissue Kit (Qiagen), following the manufacturer’s directions. .. To improve recombinant protein solubility, the N-terminus signal sequences of EscC (GenBank protein accession no. 12518466) and LomW (GenBank protein accession no. 12514345) were predicted using the SignalP 6.0 server, and the DNA segments without the predicted signal sequences were cloned into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs) restriction sites. ..

    Solubility:

    Article Title: Efficacy of EHEC gold nanoparticle vaccines evaluated with the Shiga toxin-producing Citrobacter rodentium mouse model.
    Article Snippet: EHEC (EDL933) DNA was isolated with a DNeasy Blood and Tissue Kit (Qiagen), following the manufacturer’s directions. .. To improve recombinant protein solubility, the N-termi nus signal sequences of EscC (GenBank protein accession no. 12518466) and LomW (GenBank protein accession no. 12514345) were predicted using the SignalP 6.0 server, and the DNA segments without the predicted signal sequences were cloned into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs) restriction sites. ..

    Article Title: Further Evaluation of Enterohemorrhagic Escherichia coli Gold Nanoparticle Vaccines Utilizing Citrobacter rodentium as the Model Organism
    Article Snippet: Briefly, DNA from EHEC strain EDL933 was extracted with a DNeasy Blood and Tissue kit (Qiagen, Germantown, MD, USA), according to the manufacturer’s instructions. .. To enhance solubility of recombinant EscC (GenBank protein accession no. 12518466), the N-terminal signal sequence of the protein was predicted using the SignalP 6.0 program, and the DNA segment without the predicted signal sequence was inserted in-frame with an ^X His-tag at the C-terminus into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs, Ipswich, MA, USA). ..

    Article Title: Efficacy of EHEC gold nanoparticle vaccines evaluated with the Shiga toxin-producing Citrobacter rodentium mouse model
    Article Snippet: EHEC (EDL933) DNA was isolated with a DNeasy Blood and Tissue Kit (Qiagen), following the manufacturer’s directions. .. To improve recombinant protein solubility, the N-terminus signal sequences of EscC (GenBank protein accession no. 12518466) and LomW (GenBank protein accession no. 12514345) were predicted using the SignalP 6.0 server, and the DNA segments without the predicted signal sequences were cloned into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs) restriction sites. ..

    Sequencing:

    Article Title: Further Evaluation of Enterohemorrhagic Escherichia coli Gold Nanoparticle Vaccines Utilizing Citrobacter rodentium as the Model Organism
    Article Snippet: Briefly, DNA from EHEC strain EDL933 was extracted with a DNeasy Blood and Tissue kit (Qiagen, Germantown, MD, USA), according to the manufacturer’s instructions. .. To enhance solubility of recombinant EscC (GenBank protein accession no. 12518466), the N-terminal signal sequence of the protein was predicted using the SignalP 6.0 program, and the DNA segment without the predicted signal sequence was inserted in-frame with an ^X His-tag at the C-terminus into a pET30a(+) expression vector using NdeI and XhoI (New England BioLabs, Ipswich, MA, USA). ..

    Polymerase Chain Reaction:

    Article Title: Crystal Structure of H227A Mutant of Arginine Kinase in Daphnia magna Suggests the Importance of Its Stability
    Article Snippet: These PCR products, containing mutated gene, was extracted by QIAquick Gel Extraction Kit (Hilden, Germany, QIAGEN) and utilized to second PCR step as primer with primer Dm AK-NdeI-F (Forward) and Dm AK-NotI-R, which didn’t use at first PCR. .. The mutated genes, after second PCR, were inserted into the pET30a expression vector (Ipswich, MA, USA, New England Biolabs) using a restriction enzyme of Nde I and Not I (Kusatsu, Japan, Takara). .. The recombinant plasmids of Dm AK histidine mutants (H90A, H227A, H284A and H315A) were induced to express in BL21(DE3) Escherichia coli ( E. coli ) system with 0.5 mM isopropyl β-D-1-thiogalactopyranoside (IPTG) (Haarlem, Netherlands, Duchefa Biochemie) for overnight at 20 °C and 170 rpm.



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