Review



modified pet28a(+) vector  (Millipore)


Bioz Verified Symbol Millipore is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 90

    Structured Review

    Millipore modified pet28a(+) vector
    Modified Pet28a(+) 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/modified+pet28a(+)+vector/pet28a/bio_rxiv__2024__05__15__594396-53-15-17
    Average 90 stars, based on 1 article reviews
    modified pet28a(+) vector - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Clone Assay:

    Article Title: Oligoribonuclease functions as a diribonucleotidase to bypass a key bottleneck in RNA degradation
    Article Snippet: Orn genes from Vibrio cholerae O1 El Tor VC0341 (residues 1-181) and Homo sapiens REXO2 (residues 33-237) were synthesized by Geneart (Life Technologies). .. Genes were cloned by ligation between BamHI and NotI sites of a modified pET28a vector (Novagen) yielding N-terminally His 6 -tagged small ubiquitin-like modifier (SUMO) fusion proteins cleavable by recombinant Ulp-1 protease. .. Orn proteins were overexpressed in E. coli BL21 T7 Express cells (New England Biolabs).

    Article Title: Bacterial pathogens deliver water- and solute-permeable channels to plant cells.
    Article Snippet: Cloning, expression and purification of E. amylovora DspE and DspE(Δβ-barrel) in Escherichia coli The dspE gene was PCR-amplified from the genomic DNA of E. amylovora strain Ea273 using the KOD hot start polymerase (Millipore Sigma) and the following primer set: DspE_Forward_primer: 5′-ATGGAATTAAAATCACTGGGAACTGAACACAAG -3′; DspE_Reverse_ primer: 5′-GCTCTTCATTTCCAGCCCTTCCTTC-3′. .. The PCR product was cloned into a modified pET28a vector (Millipore Sigma) as a C-terminal fusion to maltose-binding protein (MBP) containing a His8 tag, a preScission protease cleavage site (PPX) and a Flag tag in the form of MBP–His8–PPX–Flag–DspE (hereinafter as MBP–DspE). ..

    Article Title: Campylobacter hyointestinalis Isolated from Pigs Produces Multiple Variants of Biologically Active Cytolethal Distending Toxin
    Article Snippet: The cdt-IIA, cdt-IIB, and cdt-IIC genes (open reading frames [ORFs] 11 to 13 in Fig. 2; also see Table S3 in the supplemental material) were PCR amplified using the genomic DNA of C. hyointestinalis strain ATCC 35217T as the template (see Table S1). .. Each of these amplified DNA fragments was digested with either EcoRI and HindIII or EcoRI and SacI (New England Biolabs Inc.) and cloned into the region downstream of the EcoRI site of the modified pET28a vector (Novagen, New Canaan, CT). .. This vector encoded His6 sequence and a tobacco etch virus protease cleavage (TEV) 4306 iai.asm.org November 2015 Volume 83 Number 11Infection and Immunity on O ctober 12, 2015 by U N IV O F N E B R A S K A -LIN C O LN http://iai.asm .org/ D ow nloaded from sequence upstream of the EcoRI restriction site.

    Article Title: Structural characterization of NrnC identifies unifying features of dinucleases
    Article Snippet: For protein expression in Escherichia coli , codon-optimized NrnC genes from B. henselae (BH02530) and B. melitensis (BMEI1828) were synthesized by Geneart (Life Technologies). .. Genes were cloned into a modified pET28a vector (Novagen) between BamHI and NotI sites using InFusion cloning (Takara Bio). ..

    Article Title: Molecular Analysis of the Interaction between Human PTPN21 and the Oncoprotein E7 from Human Papillomavirus Genotype 18
    Article Snippet: Each of the DNA fragments encoding the human PTPN21 (residues 873-1174, referred to as PTP PTPN21 ) and human PTPN14 (residues 886-1187, referred to as PTP PTPN14 ) PTP domains were cloned into the modified pPRoEX HTa plasmid (Invitrogen, USA) with an N-terminal (His) 10 -linked green fluorescent protein tag and the pET21a plasmid (Novagen, USA), respectively. .. Each of the E7 DNA fragments encoding CR3s of HPV18 (residues 54-105, referred to as CR3 18E7 ), HPV16 (residues 45-98), HPV1a (residues 39-93), and HPV11 (residues 45-98) were cloned into the modified pET28a vector (Novagen), with an N-terminal (His) 6 -linked maltose-binding protein tag. ..

    Article Title: Structure of succinyl-CoA:3-ketoacid CoA transferase from Drosophila melanogaster
    Article Snippet: .. The amplified fragments were then cloned into a modified pET28a vector (Novagen) with an additional 6×His coding sequence following a TEV protease cleavage site at the 5′ end of the gene. .. The recombinant Dm SCOT expression plasmid was identified by restriction-endonuclease digestion and was further verified using DNA sequencing at Sangon Biotech (Shanghai, People’s Republic of China).

    Ligation:

    Article Title: Oligoribonuclease functions as a diribonucleotidase to bypass a key bottleneck in RNA degradation
    Article Snippet: Orn genes from Vibrio cholerae O1 El Tor VC0341 (residues 1-181) and Homo sapiens REXO2 (residues 33-237) were synthesized by Geneart (Life Technologies). .. Genes were cloned by ligation between BamHI and NotI sites of a modified pET28a vector (Novagen) yielding N-terminally His 6 -tagged small ubiquitin-like modifier (SUMO) fusion proteins cleavable by recombinant Ulp-1 protease. .. Orn proteins were overexpressed in E. coli BL21 T7 Express cells (New England Biolabs).

    Modification:

    Article Title: Oligoribonuclease functions as a diribonucleotidase to bypass a key bottleneck in RNA degradation
    Article Snippet: Orn genes from Vibrio cholerae O1 El Tor VC0341 (residues 1-181) and Homo sapiens REXO2 (residues 33-237) were synthesized by Geneart (Life Technologies). .. Genes were cloned by ligation between BamHI and NotI sites of a modified pET28a vector (Novagen) yielding N-terminally His 6 -tagged small ubiquitin-like modifier (SUMO) fusion proteins cleavable by recombinant Ulp-1 protease. .. Orn proteins were overexpressed in E. coli BL21 T7 Express cells (New England Biolabs).

    Article Title: Bacterial pathogens deliver water- and solute-permeable channels to plant cells.
    Article Snippet: Cloning, expression and purification of E. amylovora DspE and DspE(Δβ-barrel) in Escherichia coli The dspE gene was PCR-amplified from the genomic DNA of E. amylovora strain Ea273 using the KOD hot start polymerase (Millipore Sigma) and the following primer set: DspE_Forward_primer: 5′-ATGGAATTAAAATCACTGGGAACTGAACACAAG -3′; DspE_Reverse_ primer: 5′-GCTCTTCATTTCCAGCCCTTCCTTC-3′. .. The PCR product was cloned into a modified pET28a vector (Millipore Sigma) as a C-terminal fusion to maltose-binding protein (MBP) containing a His8 tag, a preScission protease cleavage site (PPX) and a Flag tag in the form of MBP–His8–PPX–Flag–DspE (hereinafter as MBP–DspE). ..

    Article Title: Campylobacter hyointestinalis Isolated from Pigs Produces Multiple Variants of Biologically Active Cytolethal Distending Toxin
    Article Snippet: The cdt-IIA, cdt-IIB, and cdt-IIC genes (open reading frames [ORFs] 11 to 13 in Fig. 2; also see Table S3 in the supplemental material) were PCR amplified using the genomic DNA of C. hyointestinalis strain ATCC 35217T as the template (see Table S1). .. Each of these amplified DNA fragments was digested with either EcoRI and HindIII or EcoRI and SacI (New England Biolabs Inc.) and cloned into the region downstream of the EcoRI site of the modified pET28a vector (Novagen, New Canaan, CT). .. This vector encoded His6 sequence and a tobacco etch virus protease cleavage (TEV) 4306 iai.asm.org November 2015 Volume 83 Number 11Infection and Immunity on O ctober 12, 2015 by U N IV O F N E B R A S K A -LIN C O LN http://iai.asm .org/ D ow nloaded from sequence upstream of the EcoRI restriction site.

    Article Title: The endophilin curvature-sensitive motif requires electrostatic guidance to recycle synaptic vesicles in vivo.
    Article Snippet: .. To construct plasmids for recombinant protein expression, DNA fragments encoding genes of interest were inserted into a modified PET28A vector (Novagen, Madison, WA) containing a His6 tag to facilitate purification. .. BIN1_AH [8-33, H. sapiens] VTAGKIASNVQKKLTRAQEKVLQKL 5’-gtgactgctggaaaaatagcttcaaatgtccagaagaagttgactcgtgcccaagagaaggttctccaaaaactc-3’ ARF1_AH [1-17, H. sapiens] MGNIFANLFKGLFGKKE 5’-atgggtaacatctttgccaacctgtttaaaggtctttttggcaagaaggag-3’ NUP133_AH [245-267, H. sapiens] LPQGQGMLSGIGRKVSSLFGILS 5’-cttccacaaggtcagggcatgctcagtggaattggtagaaaagtatcttcattgttcggaatcctttca-3’ KES1_AH [7-29, S. cerevisiae] SSSWTSFLKSIASFNGDLSSLSA 5’-tcatcatcctggacatctttcctgaaatctatcgcttcctttaatggtgatttgtcgtcgctgagtgcc-3’ Sar1p_AH [1-23] MAGWDIFGWFRDVLASLGLWNKH 5’-atggccggatgggacatcttcggatggttccgtgacgtccttgcctcccttggactttggaacaagcac-3’ EPN1_AH [3-16, H. sapiens] TSSLRRQMKNIVHN 5’-acgtcttcccttcgaagacagatgaaaaacatagtacataac-3’ CPX-1_AH [115-135, C. elegans] LGLTEQVEKAKTMATGAFETV 5’-ctcgggctcacggagcaagtcgaaaaagcgaaaactatggcgaccggcgccttcgagaccgtc-3’ divIVA_AH [25-41, B. subtilis] VNEFLAQVRKDYEIVLR 5’-gtcaacgagttccttgcccaagtccgtaaggactacgagatcgtcctccgt-3’ alpha-synuclein [9-52, H. sapiens] SKAKEGVVAAAEKTKQGVAEAAGKTKEGVLYVGSKTKEGVVHGV 5’-tccaaggccaaggagggagtcgtcgccgctgctgagaagactaagcaaggagttgctgaggctgctggaaagactaaggaggg agttctttacgttggatctaagacca aggagggagtcgttcacggagtc-3’

    Article Title: Structural characterization of NrnC identifies unifying features of dinucleases
    Article Snippet: For protein expression in Escherichia coli , codon-optimized NrnC genes from B. henselae (BH02530) and B. melitensis (BMEI1828) were synthesized by Geneart (Life Technologies). .. Genes were cloned into a modified pET28a vector (Novagen) between BamHI and NotI sites using InFusion cloning (Takara Bio). ..

    Article Title: Molecular Analysis of the Interaction between Human PTPN21 and the Oncoprotein E7 from Human Papillomavirus Genotype 18
    Article Snippet: Each of the DNA fragments encoding the human PTPN21 (residues 873-1174, referred to as PTP PTPN21 ) and human PTPN14 (residues 886-1187, referred to as PTP PTPN14 ) PTP domains were cloned into the modified pPRoEX HTa plasmid (Invitrogen, USA) with an N-terminal (His) 10 -linked green fluorescent protein tag and the pET21a plasmid (Novagen, USA), respectively. .. Each of the E7 DNA fragments encoding CR3s of HPV18 (residues 54-105, referred to as CR3 18E7 ), HPV16 (residues 45-98), HPV1a (residues 39-93), and HPV11 (residues 45-98) were cloned into the modified pET28a vector (Novagen), with an N-terminal (His) 6 -linked maltose-binding protein tag. ..

    Article Title: Structure of succinyl-CoA:3-ketoacid CoA transferase from Drosophila melanogaster
    Article Snippet: .. The amplified fragments were then cloned into a modified pET28a vector (Novagen) with an additional 6×His coding sequence following a TEV protease cleavage site at the 5′ end of the gene. .. The recombinant Dm SCOT expression plasmid was identified by restriction-endonuclease digestion and was further verified using DNA sequencing at Sangon Biotech (Shanghai, People’s Republic of China).

    Ubiquitin Proteomics:

    Article Title: Oligoribonuclease functions as a diribonucleotidase to bypass a key bottleneck in RNA degradation
    Article Snippet: Orn genes from Vibrio cholerae O1 El Tor VC0341 (residues 1-181) and Homo sapiens REXO2 (residues 33-237) were synthesized by Geneart (Life Technologies). .. Genes were cloned by ligation between BamHI and NotI sites of a modified pET28a vector (Novagen) yielding N-terminally His 6 -tagged small ubiquitin-like modifier (SUMO) fusion proteins cleavable by recombinant Ulp-1 protease. .. Orn proteins were overexpressed in E. coli BL21 T7 Express cells (New England Biolabs).

    Recombinant:

    Article Title: Oligoribonuclease functions as a diribonucleotidase to bypass a key bottleneck in RNA degradation
    Article Snippet: Orn genes from Vibrio cholerae O1 El Tor VC0341 (residues 1-181) and Homo sapiens REXO2 (residues 33-237) were synthesized by Geneart (Life Technologies). .. Genes were cloned by ligation between BamHI and NotI sites of a modified pET28a vector (Novagen) yielding N-terminally His 6 -tagged small ubiquitin-like modifier (SUMO) fusion proteins cleavable by recombinant Ulp-1 protease. .. Orn proteins were overexpressed in E. coli BL21 T7 Express cells (New England Biolabs).

    Article Title: The endophilin curvature-sensitive motif requires electrostatic guidance to recycle synaptic vesicles in vivo.
    Article Snippet: .. To construct plasmids for recombinant protein expression, DNA fragments encoding genes of interest were inserted into a modified PET28A vector (Novagen, Madison, WA) containing a His6 tag to facilitate purification. .. BIN1_AH [8-33, H. sapiens] VTAGKIASNVQKKLTRAQEKVLQKL 5’-gtgactgctggaaaaatagcttcaaatgtccagaagaagttgactcgtgcccaagagaaggttctccaaaaactc-3’ ARF1_AH [1-17, H. sapiens] MGNIFANLFKGLFGKKE 5’-atgggtaacatctttgccaacctgtttaaaggtctttttggcaagaaggag-3’ NUP133_AH [245-267, H. sapiens] LPQGQGMLSGIGRKVSSLFGILS 5’-cttccacaaggtcagggcatgctcagtggaattggtagaaaagtatcttcattgttcggaatcctttca-3’ KES1_AH [7-29, S. cerevisiae] SSSWTSFLKSIASFNGDLSSLSA 5’-tcatcatcctggacatctttcctgaaatctatcgcttcctttaatggtgatttgtcgtcgctgagtgcc-3’ Sar1p_AH [1-23] MAGWDIFGWFRDVLASLGLWNKH 5’-atggccggatgggacatcttcggatggttccgtgacgtccttgcctcccttggactttggaacaagcac-3’ EPN1_AH [3-16, H. sapiens] TSSLRRQMKNIVHN 5’-acgtcttcccttcgaagacagatgaaaaacatagtacataac-3’ CPX-1_AH [115-135, C. elegans] LGLTEQVEKAKTMATGAFETV 5’-ctcgggctcacggagcaagtcgaaaaagcgaaaactatggcgaccggcgccttcgagaccgtc-3’ divIVA_AH [25-41, B. subtilis] VNEFLAQVRKDYEIVLR 5’-gtcaacgagttccttgcccaagtccgtaaggactacgagatcgtcctccgt-3’ alpha-synuclein [9-52, H. sapiens] SKAKEGVVAAAEKTKQGVAEAAGKTKEGVLYVGSKTKEGVVHGV 5’-tccaaggccaaggagggagtcgtcgccgctgctgagaagactaagcaaggagttgctgaggctgctggaaagactaaggaggg agttctttacgttggatctaagacca aggagggagtcgttcacggagtc-3’

    Polymerase Chain Reaction:

    Article Title: Bacterial pathogens deliver water- and solute-permeable channels to plant cells.
    Article Snippet: Cloning, expression and purification of E. amylovora DspE and DspE(Δβ-barrel) in Escherichia coli The dspE gene was PCR-amplified from the genomic DNA of E. amylovora strain Ea273 using the KOD hot start polymerase (Millipore Sigma) and the following primer set: DspE_Forward_primer: 5′-ATGGAATTAAAATCACTGGGAACTGAACACAAG -3′; DspE_Reverse_ primer: 5′-GCTCTTCATTTCCAGCCCTTCCTTC-3′. .. The PCR product was cloned into a modified pET28a vector (Millipore Sigma) as a C-terminal fusion to maltose-binding protein (MBP) containing a His8 tag, a preScission protease cleavage site (PPX) and a Flag tag in the form of MBP–His8–PPX–Flag–DspE (hereinafter as MBP–DspE). ..

    Article Title: Bacterial pathogens deliver water- and solute-permeable channels to plant cells
    Article Snippet: The dspE gene was PCR-amplified from the genomic DNA of E. amylovora strain Ea273 using the KOD hot start polymerase (Millipore Sigma) and the following primer set: DspE_Forward_primer: 5′-ATGGAATTAAAATCACTGGGAACTGAACACAAG -3′; DspE_Reverse_primer: 5′-GCTCTTCATTTCCAGCCCTTCCTTC-3′. .. The PCR product was cloned into a modified pET28a vector (Millipore Sigma) as a C-terminal fusion to maltose-binding protein (MBP) containing a His 8 tag, a preScission protease cleavage site (PPX) and a Flag tag in the form of MBP–His 8 –PPX–Flag–DspE (hereinafter as MBP–DspE). ..

    Plasmid Preparation:

    Article Title: Bacterial pathogens deliver water- and solute-permeable channels to plant cells.
    Article Snippet: Cloning, expression and purification of E. amylovora DspE and DspE(Δβ-barrel) in Escherichia coli The dspE gene was PCR-amplified from the genomic DNA of E. amylovora strain Ea273 using the KOD hot start polymerase (Millipore Sigma) and the following primer set: DspE_Forward_primer: 5′-ATGGAATTAAAATCACTGGGAACTGAACACAAG -3′; DspE_Reverse_ primer: 5′-GCTCTTCATTTCCAGCCCTTCCTTC-3′. .. The PCR product was cloned into a modified pET28a vector (Millipore Sigma) as a C-terminal fusion to maltose-binding protein (MBP) containing a His8 tag, a preScission protease cleavage site (PPX) and a Flag tag in the form of MBP–His8–PPX–Flag–DspE (hereinafter as MBP–DspE). ..

    Article Title: Structural characterization of NrnC identifies unifying features of dinucleases
    Article Snippet: For protein expression in Escherichia coli , codon-optimized NrnC genes from B. henselae (BH02530) and B. melitensis (BMEI1828) were synthesized by Geneart (Life Technologies). .. Genes were cloned into a modified pET28a vector (Novagen) between BamHI and NotI sites using InFusion cloning (Takara Bio). ..

    Article Title: Molecular Analysis of the Interaction between Human PTPN21 and the Oncoprotein E7 from Human Papillomavirus Genotype 18
    Article Snippet: Each of the DNA fragments encoding the human PTPN21 (residues 873-1174, referred to as PTP PTPN21 ) and human PTPN14 (residues 886-1187, referred to as PTP PTPN14 ) PTP domains were cloned into the modified pPRoEX HTa plasmid (Invitrogen, USA) with an N-terminal (His) 10 -linked green fluorescent protein tag and the pET21a plasmid (Novagen, USA), respectively. .. Each of the E7 DNA fragments encoding CR3s of HPV18 (residues 54-105, referred to as CR3 18E7 ), HPV16 (residues 45-98), HPV1a (residues 39-93), and HPV11 (residues 45-98) were cloned into the modified pET28a vector (Novagen), with an N-terminal (His) 6 -linked maltose-binding protein tag. ..

    Article Title: Bacterial pathogens deliver water- and solute-permeable channels to plant cells
    Article Snippet: The dspE gene was PCR-amplified from the genomic DNA of E. amylovora strain Ea273 using the KOD hot start polymerase (Millipore Sigma) and the following primer set: DspE_Forward_primer: 5′-ATGGAATTAAAATCACTGGGAACTGAACACAAG -3′; DspE_Reverse_primer: 5′-GCTCTTCATTTCCAGCCCTTCCTTC-3′. .. The PCR product was cloned into a modified pET28a vector (Millipore Sigma) as a C-terminal fusion to maltose-binding protein (MBP) containing a His 8 tag, a preScission protease cleavage site (PPX) and a Flag tag in the form of MBP–His 8 –PPX–Flag–DspE (hereinafter as MBP–DspE). ..

    Article Title: Structure of succinyl-CoA:3-ketoacid CoA transferase from Drosophila melanogaster
    Article Snippet: .. The amplified fragments were then cloned into a modified pET28a vector (Novagen) with an additional 6×His coding sequence following a TEV protease cleavage site at the 5′ end of the gene. .. The recombinant Dm SCOT expression plasmid was identified by restriction-endonuclease digestion and was further verified using DNA sequencing at Sangon Biotech (Shanghai, People’s Republic of China).

    FLAG-tag:

    Article Title: Bacterial pathogens deliver water- and solute-permeable channels to plant cells.
    Article Snippet: Cloning, expression and purification of E. amylovora DspE and DspE(Δβ-barrel) in Escherichia coli The dspE gene was PCR-amplified from the genomic DNA of E. amylovora strain Ea273 using the KOD hot start polymerase (Millipore Sigma) and the following primer set: DspE_Forward_primer: 5′-ATGGAATTAAAATCACTGGGAACTGAACACAAG -3′; DspE_Reverse_ primer: 5′-GCTCTTCATTTCCAGCCCTTCCTTC-3′. .. The PCR product was cloned into a modified pET28a vector (Millipore Sigma) as a C-terminal fusion to maltose-binding protein (MBP) containing a His8 tag, a preScission protease cleavage site (PPX) and a Flag tag in the form of MBP–His8–PPX–Flag–DspE (hereinafter as MBP–DspE). ..

    Article Title: Bacterial pathogens deliver water- and solute-permeable channels to plant cells
    Article Snippet: The dspE gene was PCR-amplified from the genomic DNA of E. amylovora strain Ea273 using the KOD hot start polymerase (Millipore Sigma) and the following primer set: DspE_Forward_primer: 5′-ATGGAATTAAAATCACTGGGAACTGAACACAAG -3′; DspE_Reverse_primer: 5′-GCTCTTCATTTCCAGCCCTTCCTTC-3′. .. The PCR product was cloned into a modified pET28a vector (Millipore Sigma) as a C-terminal fusion to maltose-binding protein (MBP) containing a His 8 tag, a preScission protease cleavage site (PPX) and a Flag tag in the form of MBP–His 8 –PPX–Flag–DspE (hereinafter as MBP–DspE). ..

    Amplification:

    Article Title: Campylobacter hyointestinalis Isolated from Pigs Produces Multiple Variants of Biologically Active Cytolethal Distending Toxin
    Article Snippet: The cdt-IIA, cdt-IIB, and cdt-IIC genes (open reading frames [ORFs] 11 to 13 in Fig. 2; also see Table S3 in the supplemental material) were PCR amplified using the genomic DNA of C. hyointestinalis strain ATCC 35217T as the template (see Table S1). .. Each of these amplified DNA fragments was digested with either EcoRI and HindIII or EcoRI and SacI (New England Biolabs Inc.) and cloned into the region downstream of the EcoRI site of the modified pET28a vector (Novagen, New Canaan, CT). .. This vector encoded His6 sequence and a tobacco etch virus protease cleavage (TEV) 4306 iai.asm.org November 2015 Volume 83 Number 11Infection and Immunity on O ctober 12, 2015 by U N IV O F N E B R A S K A -LIN C O LN http://iai.asm .org/ D ow nloaded from sequence upstream of the EcoRI restriction site.

    Article Title: Structure of succinyl-CoA:3-ketoacid CoA transferase from Drosophila melanogaster
    Article Snippet: .. The amplified fragments were then cloned into a modified pET28a vector (Novagen) with an additional 6×His coding sequence following a TEV protease cleavage site at the 5′ end of the gene. .. The recombinant Dm SCOT expression plasmid was identified by restriction-endonuclease digestion and was further verified using DNA sequencing at Sangon Biotech (Shanghai, People’s Republic of China).

    Construct:

    Article Title: The endophilin curvature-sensitive motif requires electrostatic guidance to recycle synaptic vesicles in vivo.
    Article Snippet: .. To construct plasmids for recombinant protein expression, DNA fragments encoding genes of interest were inserted into a modified PET28A vector (Novagen, Madison, WA) containing a His6 tag to facilitate purification. .. BIN1_AH [8-33, H. sapiens] VTAGKIASNVQKKLTRAQEKVLQKL 5’-gtgactgctggaaaaatagcttcaaatgtccagaagaagttgactcgtgcccaagagaaggttctccaaaaactc-3’ ARF1_AH [1-17, H. sapiens] MGNIFANLFKGLFGKKE 5’-atgggtaacatctttgccaacctgtttaaaggtctttttggcaagaaggag-3’ NUP133_AH [245-267, H. sapiens] LPQGQGMLSGIGRKVSSLFGILS 5’-cttccacaaggtcagggcatgctcagtggaattggtagaaaagtatcttcattgttcggaatcctttca-3’ KES1_AH [7-29, S. cerevisiae] SSSWTSFLKSIASFNGDLSSLSA 5’-tcatcatcctggacatctttcctgaaatctatcgcttcctttaatggtgatttgtcgtcgctgagtgcc-3’ Sar1p_AH [1-23] MAGWDIFGWFRDVLASLGLWNKH 5’-atggccggatgggacatcttcggatggttccgtgacgtccttgcctcccttggactttggaacaagcac-3’ EPN1_AH [3-16, H. sapiens] TSSLRRQMKNIVHN 5’-acgtcttcccttcgaagacagatgaaaaacatagtacataac-3’ CPX-1_AH [115-135, C. elegans] LGLTEQVEKAKTMATGAFETV 5’-ctcgggctcacggagcaagtcgaaaaagcgaaaactatggcgaccggcgccttcgagaccgtc-3’ divIVA_AH [25-41, B. subtilis] VNEFLAQVRKDYEIVLR 5’-gtcaacgagttccttgcccaagtccgtaaggactacgagatcgtcctccgt-3’ alpha-synuclein [9-52, H. sapiens] SKAKEGVVAAAEKTKQGVAEAAGKTKEGVLYVGSKTKEGVVHGV 5’-tccaaggccaaggagggagtcgtcgccgctgctgagaagactaagcaaggagttgctgaggctgctggaaagactaaggaggg agttctttacgttggatctaagacca aggagggagtcgttcacggagtc-3’

    Expressing:

    Article Title: The endophilin curvature-sensitive motif requires electrostatic guidance to recycle synaptic vesicles in vivo.
    Article Snippet: .. To construct plasmids for recombinant protein expression, DNA fragments encoding genes of interest were inserted into a modified PET28A vector (Novagen, Madison, WA) containing a His6 tag to facilitate purification. .. BIN1_AH [8-33, H. sapiens] VTAGKIASNVQKKLTRAQEKVLQKL 5’-gtgactgctggaaaaatagcttcaaatgtccagaagaagttgactcgtgcccaagagaaggttctccaaaaactc-3’ ARF1_AH [1-17, H. sapiens] MGNIFANLFKGLFGKKE 5’-atgggtaacatctttgccaacctgtttaaaggtctttttggcaagaaggag-3’ NUP133_AH [245-267, H. sapiens] LPQGQGMLSGIGRKVSSLFGILS 5’-cttccacaaggtcagggcatgctcagtggaattggtagaaaagtatcttcattgttcggaatcctttca-3’ KES1_AH [7-29, S. cerevisiae] SSSWTSFLKSIASFNGDLSSLSA 5’-tcatcatcctggacatctttcctgaaatctatcgcttcctttaatggtgatttgtcgtcgctgagtgcc-3’ Sar1p_AH [1-23] MAGWDIFGWFRDVLASLGLWNKH 5’-atggccggatgggacatcttcggatggttccgtgacgtccttgcctcccttggactttggaacaagcac-3’ EPN1_AH [3-16, H. sapiens] TSSLRRQMKNIVHN 5’-acgtcttcccttcgaagacagatgaaaaacatagtacataac-3’ CPX-1_AH [115-135, C. elegans] LGLTEQVEKAKTMATGAFETV 5’-ctcgggctcacggagcaagtcgaaaaagcgaaaactatggcgaccggcgccttcgagaccgtc-3’ divIVA_AH [25-41, B. subtilis] VNEFLAQVRKDYEIVLR 5’-gtcaacgagttccttgcccaagtccgtaaggactacgagatcgtcctccgt-3’ alpha-synuclein [9-52, H. sapiens] SKAKEGVVAAAEKTKQGVAEAAGKTKEGVLYVGSKTKEGVVHGV 5’-tccaaggccaaggagggagtcgtcgccgctgctgagaagactaagcaaggagttgctgaggctgctggaaagactaaggaggg agttctttacgttggatctaagacca aggagggagtcgttcacggagtc-3’

    Purification:

    Article Title: The endophilin curvature-sensitive motif requires electrostatic guidance to recycle synaptic vesicles in vivo.
    Article Snippet: .. To construct plasmids for recombinant protein expression, DNA fragments encoding genes of interest were inserted into a modified PET28A vector (Novagen, Madison, WA) containing a His6 tag to facilitate purification. .. BIN1_AH [8-33, H. sapiens] VTAGKIASNVQKKLTRAQEKVLQKL 5’-gtgactgctggaaaaatagcttcaaatgtccagaagaagttgactcgtgcccaagagaaggttctccaaaaactc-3’ ARF1_AH [1-17, H. sapiens] MGNIFANLFKGLFGKKE 5’-atgggtaacatctttgccaacctgtttaaaggtctttttggcaagaaggag-3’ NUP133_AH [245-267, H. sapiens] LPQGQGMLSGIGRKVSSLFGILS 5’-cttccacaaggtcagggcatgctcagtggaattggtagaaaagtatcttcattgttcggaatcctttca-3’ KES1_AH [7-29, S. cerevisiae] SSSWTSFLKSIASFNGDLSSLSA 5’-tcatcatcctggacatctttcctgaaatctatcgcttcctttaatggtgatttgtcgtcgctgagtgcc-3’ Sar1p_AH [1-23] MAGWDIFGWFRDVLASLGLWNKH 5’-atggccggatgggacatcttcggatggttccgtgacgtccttgcctcccttggactttggaacaagcac-3’ EPN1_AH [3-16, H. sapiens] TSSLRRQMKNIVHN 5’-acgtcttcccttcgaagacagatgaaaaacatagtacataac-3’ CPX-1_AH [115-135, C. elegans] LGLTEQVEKAKTMATGAFETV 5’-ctcgggctcacggagcaagtcgaaaaagcgaaaactatggcgaccggcgccttcgagaccgtc-3’ divIVA_AH [25-41, B. subtilis] VNEFLAQVRKDYEIVLR 5’-gtcaacgagttccttgcccaagtccgtaaggactacgagatcgtcctccgt-3’ alpha-synuclein [9-52, H. sapiens] SKAKEGVVAAAEKTKQGVAEAAGKTKEGVLYVGSKTKEGVVHGV 5’-tccaaggccaaggagggagtcgtcgccgctgctgagaagactaagcaaggagttgctgaggctgctggaaagactaaggaggg agttctttacgttggatctaagacca aggagggagtcgttcacggagtc-3’

    Cloning:

    Article Title: Structural characterization of NrnC identifies unifying features of dinucleases
    Article Snippet: For protein expression in Escherichia coli , codon-optimized NrnC genes from B. henselae (BH02530) and B. melitensis (BMEI1828) were synthesized by Geneart (Life Technologies). .. Genes were cloned into a modified pET28a vector (Novagen) between BamHI and NotI sites using InFusion cloning (Takara Bio). ..

    Sequencing:

    Article Title: Structure of succinyl-CoA:3-ketoacid CoA transferase from Drosophila melanogaster
    Article Snippet: .. The amplified fragments were then cloned into a modified pET28a vector (Novagen) with an additional 6×His coding sequence following a TEV protease cleavage site at the 5′ end of the gene. .. The recombinant Dm SCOT expression plasmid was identified by restriction-endonuclease digestion and was further verified using DNA sequencing at Sangon Biotech (Shanghai, People’s Republic of China).



    Similar Products

    90
    Millipore modified pet28a(+) vector
    Modified Pet28a(+) 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/modified+pet28a(+)+vector/pet28a/bio_rxiv__2024__05__15__594396-53-15-17
    Average 90 stars, based on 1 article reviews
    modified pet28a(+) vector - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

    90
    Millipore modified pet28a expression vector
    Modified Pet28a Expression 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/modified+pet28a(+)+vector/pet28a/pm38654065-241-22-25
    Average 90 stars, based on 1 article reviews
    modified pet28a expression vector - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

    90
    Millipore modified pet28a vector containing an n- terminal his6sumo- tag
    Modified Pet28a Vector Containing An N Terminal His6sumo Tag, 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/modified+pet28a(+)+vector/pet28a/10__7554_slash_elife__86847-362-47-22
    Average 90 stars, based on 1 article reviews
    modified pet28a vector containing an n- terminal his6sumo- tag - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

    90
    Millipore modified pet28a vector
    Modified Pet28a 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/modified+pet28a(+)+vector/pet28a/pm37704725-340-8-10
    Average 90 stars, based on 1 article reviews
    modified pet28a vector - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

    90
    Millipore modified pet28a vectors
    Modified Pet28a Vectors, 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/modified+pet28a(+)+vector/pet28a/pm36709343-266-18-20
    Average 90 stars, based on 1 article reviews
    modified pet28a vectors - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

    90
    Thermo Fisher modified pet28a expression vector
    Modified Pet28a Expression Vector, supplied by Thermo Fisher, 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/modified+pet28a(+)+vector/pm36333308-177-29-32
    Average 90 stars, based on 1 article reviews
    modified pet28a expression vector - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

    Image Search Results