accuprimetm pfx supermix (Thermo Fisher)
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accuprimetm pfx supermix
Accuprimetm Pfx Supermix, 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/pfx+supermix/accuprimetm+pfx+supermix/pmc10483636__pnas__2303574120__sapp-211-19-24
Average 90 stars, based on 1 article reviews
Accuprimetm Pfx Supermix, 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/pfx+supermix/accuprimetm+pfx+supermix/pmc10483636__pnas__2303574120__sapp-211-19-24
Average 90 stars, based on 1 article reviews
accuprimetm pfx supermix - by Bioz Stars,
2026-10
90/100 stars
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Amplification:Article Title: Transcriptome-Wide Identification of Hfq-Associated RNAs in Brucella suis by Deep Sequencing Article Snippet: .. The hfq gene and ∼1 kb of the upstream flanking region were amplified by using oligonucleotide primers hfq -Up-FLAG-For and hfq -Up-FLAG-Rev (all primers are listed in Table S1 in the supplemental material), B. suis 1330 genomic DNA, and Article Title: Glutathione Transport: A New Role for PfCRT in Chloroquine Resistance Article Snippet: The chimeric genes were expressed under the control of the Pfhsp86 promoter and were generated using the Invitrogen MultiSite Gateway system in combination with the pCHD-3/4 destination vector ( 48 ). .. To generate gene entry clones, the full-length genes for γ gcs and gs were amplified using the primer pairs, defined in , using Article Title: The stem region of group A transferase is crucial for its specificity, and its alteration promotes heterologous Forssman synthase activity Article Snippet: Plasmid pRK5-B4GALT1(1–81)-mTagBFP2 CDS was created by switching the fluorescent protein of pRK5-B4GALT1(1–81)-EGFP by mTagBFP2 from and pmTag-BFP2 (Addgene) plasmid using Bam HI/ Not I restriction sites. .. Tagged mFS, hAT, and hAT constructs were constructed by amplifying the coding regions, eliminating the stop codon, and adding the required tag by PCR amplification using Article Title: Transcriptomic and biochemical analyses identify a family of chlorhexidine efflux proteins Article Snippet: .. Genes were amplified by PCR with Mutagenesis:Article Title: Quaternary Epitope Specificities of Anti-HIV-1 Neutralizing Antibodies Generated in Rhesus Macaques Infected by the Simian/Human Immunodeficiency Virus SHIV SF162P4 Article Snippet: .. The mutagenesis reaction mixtures consisted of 25 ng of template DNA, a 0.4 M concentration of each mutagenesis primer, and Article Title: Quaternary Epitope Specificities of Anti-HIV-1 Neutralizing Antibodies Generated in Rhesus Macaques Infected by the Simian/Human Immunodeficiency Virus SHIV SF162P4 Article Snippet: .. The mutagenesis reaction mixtures consisted of 25 ng of template DNA, a 0.4 μM concentration of each mutagenesis primer, and Concentration Assay:Article Title: Quaternary Epitope Specificities of Anti-HIV-1 Neutralizing Antibodies Generated in Rhesus Macaques Infected by the Simian/Human Immunodeficiency Virus SHIV SF162P4 Article Snippet: .. The mutagenesis reaction mixtures consisted of 25 ng of template DNA, a 0.4 M concentration of each mutagenesis primer, and Article Title: Quaternary Epitope Specificities of Anti-HIV-1 Neutralizing Antibodies Generated in Rhesus Macaques Infected by the Simian/Human Immunodeficiency Virus SHIV SF162P4 Article Snippet: .. The mutagenesis reaction mixtures consisted of 25 ng of template DNA, a 0.4 μM concentration of each mutagenesis primer, and Clone Assay:Article Title: Glutathione Transport: A New Role for PfCRT in Chloroquine Resistance Article Snippet: The chimeric genes were expressed under the control of the Pfhsp86 promoter and were generated using the Invitrogen MultiSite Gateway system in combination with the pCHD-3/4 destination vector ( 48 ). .. To generate gene entry clones, the full-length genes for γ gcs and gs were amplified using the primer pairs, defined in , using Article Title: Transcriptomic and biochemical analyses identify a family of chlorhexidine efflux proteins Article Snippet: .. Genes were amplified by PCR with Construct:Article Title: The stem region of group A transferase is crucial for its specificity, and its alteration promotes heterologous Forssman synthase activity Article Snippet: Plasmid pRK5-B4GALT1(1–81)-mTagBFP2 CDS was created by switching the fluorescent protein of pRK5-B4GALT1(1–81)-EGFP by mTagBFP2 from and pmTag-BFP2 (Addgene) plasmid using Bam HI/ Not I restriction sites. .. 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Genes were amplified by PCR with Article Title: Engineering Hyperthermophilic Archaeon Pyrococcus furiosus to Overproduce Its Cytoplasmic [NiFe]-Hydrogenase Article Snippet: .. PCR products were purified using a commercial extraction protocol (Stratagene, Santa Clara, CA) and were used in overlapping PCR reactions using the Purification:Article Title: Engineering Hyperthermophilic Archaeon Pyrococcus furiosus to Overproduce Its Cytoplasmic [NiFe]-Hydrogenase Article Snippet: .. PCR products were purified using a commercial extraction protocol (Stratagene, Santa Clara, CA) and were used in overlapping PCR reactions using the Extraction:Article Title: Engineering Hyperthermophilic Archaeon Pyrococcus furiosus to Overproduce Its Cytoplasmic [NiFe]-Hydrogenase Article Snippet: .. PCR products were purified using a commercial extraction protocol (Stratagene, Santa Clara, CA) and were used in overlapping PCR reactions using the Plasmid Preparation:Article Title: The stem region of group A transferase is crucial for its specificity, and its alteration promotes heterologous Forssman synthase activity. Article Snippet: Plasmid pRK5-B4GALT1(1– 81)-mTagBFP2 CDS was created by switching the fluorescent protein of pRK5-B4GALT1(1–81)-EGFP58 by mTagBFP2 from and pmTag-BFP2 (Addgene) plasmid using BamHI/NotI restriction sites. .. Tagged mFS, hAT, and hAT constructs were constructed by amplifying the coding regions, eliminating the stop codon, and adding the required tag by PCR amplification using |