pbluescript vector (New England Biolabs)
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New England Biolabs
pbluescript vector
Pbluescript Vector, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 6905 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pbluescript+vectors/XbaI/pmc12228689-243-36-41
Average 99 stars, based on 6905 article reviews
Pbluescript Vector, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 6905 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pbluescript+vectors/XbaI/pmc12228689-243-36-41
Average 99 stars, based on 6905 article reviews
pbluescript vector - by Bioz Stars,
2026-10
99/100 stars
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Sterility:Article Title: Risk factors for in vivo emergence of ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae and the associated resistance mechanisms: a case-control study. Article Snippet: .. The plugs were then washed with sterile water and TE buffer at 56°C to remove proteinase K. Following digestion of plugs with the Agarose Gel Electrophoresis:Article Title: Risk factors for in vivo emergence of ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae and the associated resistance mechanisms: a case-control study. Article Snippet: .. The plugs were then washed with sterile water and TE buffer at 56°C to remove proteinase K. Following digestion of plugs with the Article Title: Regulation of Tau Alternative Splicing: A Novel Role for the Ribonucleoprotein RBM20. Article Snippet: The genomic regions identified by bioinformatic analysis (see Section 4.1) were amplified via high-fidelity PCR using the PhusionTM High-Fidelity DNA Polymerase (cat F530S, Thermo Fisher Scientific, Waltham, MA, USA) using sequence-specific primers (see Section 4.14), including restriction sites for XbaI and SalI enzymes at their 5′-ends. .. The PCR product, extracted from the agarose gel using the QIAquick Gel Extraction Kit (cat 28704, Qiagen, Venlo, The Netherlands), and the RHCglo vector was enzymatically cut using Construct:Article Title: IscR-mediated morphological regulation confers virulence and stress resistance by reducing stress molecule uptake in Acinetobacter baumannii Article Snippet: .. To construct reporter plasmids (pLPV1Z-P pbp1a and pLPV1Z-P isc operon ), promoter regions of the pbp1a operon and the isc operon, respectively, were amplified using the primers listed in Table S2 ( ). pLPV1Z was digested with PstI and Amplification:Article Title: IscR-mediated morphological regulation confers virulence and stress resistance by reducing stress molecule uptake in Acinetobacter baumannii Article Snippet: .. To construct reporter plasmids (pLPV1Z-P pbp1a and pLPV1Z-P isc operon ), promoter regions of the pbp1a operon and the isc operon, respectively, were amplified using the primers listed in Table S2 ( ). pLPV1Z was digested with PstI and Article Title: CLASHub is an integrated database and analytical platform for microRNA-target interactions. Article Snippet: .. The 3ʹ UTR fragments of human FAM3C, ZBTB4, and ZNF367 containing predicted miR-18a-5p binding sites were amplified and cloned into the pmirGLO Dual-Luciferase miRNA Target Expression Vector using the other:Article Title: Cannabinoid CB 2 receptor drives trastuzumab resistance and predicts durable anti-HER2 response. Article Snippet: DNA encoding HER2 (Uni Prot ID:P04626) was from Addgene (plasmid #16257). Binding Assay:Article Title: CLASHub is an integrated database and analytical platform for microRNA-target interactions. Article Snippet: .. The 3ʹ UTR fragments of human FAM3C, ZBTB4, and ZNF367 containing predicted miR-18a-5p binding sites were amplified and cloned into the pmirGLO Dual-Luciferase miRNA Target Expression Vector using the Clone Assay:Article Title: CLASHub is an integrated database and analytical platform for microRNA-target interactions. Article Snippet: .. The 3ʹ UTR fragments of human FAM3C, ZBTB4, and ZNF367 containing predicted miR-18a-5p binding sites were amplified and cloned into the pmirGLO Dual-Luciferase miRNA Target Expression Vector using the Expressing:Article Title: CLASHub is an integrated database and analytical platform for microRNA-target interactions. Article Snippet: .. The 3ʹ UTR fragments of human FAM3C, ZBTB4, and ZNF367 containing predicted miR-18a-5p binding sites were amplified and cloned into the pmirGLO Dual-Luciferase miRNA Target Expression Vector using the Ligation:Article Title: Magnetogenetic control of endogenous calcium signaling via ROS-sensitive ion channels reveals astrocytic regulation of neural circuit activity Article Snippet: PCR amplification of lck–D5–mScarlet-I with 5’ EcoRI and 3’ XbaI restriction sites were performed with SuperFi II (Invitrogen 12349050). .. After restriction digest with EcoRI (NEB R3101) and Transformation Assay:Article Title: Magnetogenetic control of endogenous calcium signaling via ROS-sensitive ion channels reveals astrocytic regulation of neural circuit activity Article Snippet: PCR amplification of lck–D5–mScarlet-I with 5’ EcoRI and 3’ XbaI restriction sites were performed with SuperFi II (Invitrogen 12349050). .. After restriction digest with EcoRI (NEB R3101) and Polymerase Chain Reaction:Article Title: Regulation of Tau Alternative Splicing: A Novel Role for the Ribonucleoprotein RBM20. Article Snippet: The genomic regions identified by bioinformatic analysis (see Section 4.1) were amplified via high-fidelity PCR using the PhusionTM High-Fidelity DNA Polymerase (cat F530S, Thermo Fisher Scientific, Waltham, MA, USA) using sequence-specific primers (see Section 4.14), including restriction sites for XbaI and SalI enzymes at their 5′-ends. .. The PCR product, extracted from the agarose gel using the QIAquick Gel Extraction Kit (cat 28704, Qiagen, Venlo, The Netherlands), and the RHCglo vector was enzymatically cut using Gel Extraction:Article Title: Regulation of Tau Alternative Splicing: A Novel Role for the Ribonucleoprotein RBM20. Article Snippet: The genomic regions identified by bioinformatic analysis (see Section 4.1) were amplified via high-fidelity PCR using the PhusionTM High-Fidelity DNA Polymerase (cat F530S, Thermo Fisher Scientific, Waltham, MA, USA) using sequence-specific primers (see Section 4.14), including restriction sites for XbaI and SalI enzymes at their 5′-ends. .. The PCR product, extracted from the agarose gel using the QIAquick Gel Extraction Kit (cat 28704, Qiagen, Venlo, The Netherlands), and the RHCglo vector was enzymatically cut using |