pet21e vector (Millipore)
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90
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Millipore
pet21e vector
Pet21e 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/pet21+vector/pet28a/pmc10974603-254-1-9
Average 90 stars, based on 1 article reviews
Pet21e 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/pet21+vector/pet28a/pmc10974603-254-1-9
Average 90 stars, based on 1 article reviews
pet21e vector - by Bioz Stars,
2026-09
90/100 stars
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Expressing:Article Title: Therapeutic compounds and methods Article Snippet: .. Protein Expression and Purification The catalytic domain (Gly106-Gly263) of human macrophage metalloelastase (hMMP-12), was expressed by cloning the gene into a Article Title: Complete 1 H, 13 C, 15 N resonance assignments and secondary structure of the Vpr binding region of hHR23A (residues 223-363) Article Snippet: .. The expression construct encodes the C-terminal region (residues 223–363) of hHR23A, inserted into the Article Title: Three-stage biochemical selection: cloning of prototype class IIS/IIC/IIG restriction endonuclease-methyltransferase TsoI from the thermophile Thermus scotoductus Article Snippet: .. The expression vector pET21NS (Fermentas) was a modification of the Article Title: Crystal structure of an FIV/HIV chimeric protease complexed with the broad-based inhibitor, TL-3 Article Snippet: .. All protease constructs were over-expressed in E. coli strain BL21.DE3/pLysS using T7-driven expression in the context of the Article Title: Dual role of the colonization factor CD2831 in Clostridium difficile pathogenesis Article Snippet: .. For the expression of recombinant CD2831, the corresponding full-length sequences (aa 32–940) was amplified by PCR using chromosomal DNA from C. difficile as template (primers listed in table ) and cloned into Purification:Article Title: Therapeutic compounds and methods Article Snippet: .. Protein Expression and Purification The catalytic domain (Gly106-Gly263) of human macrophage metalloelastase (hMMP-12), was expressed by cloning the gene into a Cloning:Article Title: Therapeutic compounds and methods Article Snippet: .. Protein Expression and Purification The catalytic domain (Gly106-Gly263) of human macrophage metalloelastase (hMMP-12), was expressed by cloning the gene into a Article Title: Computationally-guided design and affinity improvement of a protein binder targeting a specific site on HER2 Article Snippet: Computationally designed repebody genes and primers used for phage display library were synthesized from Integrated DNA Technologies (Coralville, IA, USA). .. Synthesized gene fragments went through cloning process after overnight digestion with restriction enzymes (Nde I, Xho I) at 37 °C and ligation (T4 DNA Ligase, Takara Bio, Shiga, Japan) into Article Title: Therapeutic Targeting of MMP-12 for the Treatment of Chronic Obstructive Pulmonary Disease Article Snippet: .. The catalytic domain (Gly106-Gly263) of human macrophage metalloelastase (hMMP-12), was expressed by cloning the gene into a Plasmid Preparation:Article Title: Therapeutic compounds and methods Article Snippet: .. Protein Expression and Purification The catalytic domain (Gly106-Gly263) of human macrophage metalloelastase (hMMP-12), was expressed by cloning the gene into a Article Title: Complete 1 H, 13 C, 15 N resonance assignments and secondary structure of the Vpr binding region of hHR23A (residues 223-363) Article Snippet: .. The expression construct encodes the C-terminal region (residues 223–363) of hHR23A, inserted into the Article Title: Crystal structure of an FIV/HIV chimeric protease complexed with the broad-based inhibitor, TL-3 Article Snippet: .. All protease constructs were over-expressed in E. coli strain BL21.DE3/pLysS using T7-driven expression in the context of the Article Title: Therapeutic Targeting of MMP-12 for the Treatment of Chronic Obstructive Pulmonary Disease Article Snippet: .. The catalytic domain (Gly106-Gly263) of human macrophage metalloelastase (hMMP-12), was expressed by cloning the gene into a Transfection:Article Title: Therapeutic compounds and methods Article Snippet: .. Protein Expression and Purification The catalytic domain (Gly106-Gly263) of human macrophage metalloelastase (hMMP-12), was expressed by cloning the gene into a Article Title: Therapeutic Targeting of MMP-12 for the Treatment of Chronic Obstructive Pulmonary Disease Article Snippet: .. The catalytic domain (Gly106-Gly263) of human macrophage metalloelastase (hMMP-12), was expressed by cloning the gene into a Synthesized:Article Title: Computationally-guided design and affinity improvement of a protein binder targeting a specific site on HER2 Article Snippet: Computationally designed repebody genes and primers used for phage display library were synthesized from Integrated DNA Technologies (Coralville, IA, USA). .. Synthesized gene fragments went through cloning process after overnight digestion with restriction enzymes (Nde I, Xho I) at 37 °C and ligation (T4 DNA Ligase, Takara Bio, Shiga, Japan) into Ligation:Article Title: Computationally-guided design and affinity improvement of a protein binder targeting a specific site on HER2 Article Snippet: Computationally designed repebody genes and primers used for phage display library were synthesized from Integrated DNA Technologies (Coralville, IA, USA). .. Synthesized gene fragments went through cloning process after overnight digestion with restriction enzymes (Nde I, Xho I) at 37 °C and ligation (T4 DNA Ligase, Takara Bio, Shiga, Japan) into Clone Assay:Article Title: Methods and kits for using recombinant microorganisms as direct reagents in biological applications Article Snippet: .. For some experiments, the coding sequences for wildtype and exonuclease deficient versions of RTX were cloned downstream of the T7 promoter in the Article Title: Dual role of the colonization factor CD2831 in Clostridium difficile pathogenesis Article Snippet: .. For the expression of recombinant CD2831, the corresponding full-length sequences (aa 32–940) was amplified by PCR using chromosomal DNA from C. difficile as template (primers listed in table ) and cloned into Construct:Article Title: Complete 1 H, 13 C, 15 N resonance assignments and secondary structure of the Vpr binding region of hHR23A (residues 223-363) Article Snippet: .. The expression construct encodes the C-terminal region (residues 223–363) of hHR23A, inserted into the Article Title: Crystal structure of an FIV/HIV chimeric protease complexed with the broad-based inhibitor, TL-3 Article Snippet: .. All protease constructs were over-expressed in E. coli strain BL21.DE3/pLysS using T7-driven expression in the context of the Modification:Article Title: Three-stage biochemical selection: cloning of prototype class IIS/IIC/IIG restriction endonuclease-methyltransferase TsoI from the thermophile Thermus scotoductus Article Snippet: .. The expression vector pET21NS (Fermentas) was a modification of the Recombinant:Article Title: Dual role of the colonization factor CD2831 in Clostridium difficile pathogenesis Article Snippet: .. For the expression of recombinant CD2831, the corresponding full-length sequences (aa 32–940) was amplified by PCR using chromosomal DNA from C. difficile as template (primers listed in table ) and cloned into Amplification:Article Title: Dual role of the colonization factor CD2831 in Clostridium difficile pathogenesis Article Snippet: .. For the expression of recombinant CD2831, the corresponding full-length sequences (aa 32–940) was amplified by PCR using chromosomal DNA from C. difficile as template (primers listed in table ) and cloned into Polymerase Chain Reaction:Article Title: Dual role of the colonization factor CD2831 in Clostridium difficile pathogenesis Article Snippet: .. For the expression of recombinant CD2831, the corresponding full-length sequences (aa 32–940) was amplified by PCR using chromosomal DNA from C. difficile as template (primers listed in table ) and cloned into |
