ex taq dna polymerase (TaKaRa)
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ex taq dna polymerase
Ex Taq Dna Polymerase, supplied by TaKaRa, used in various techniques. Bioz Stars score: 98/100, based on 16023 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ex+taq+polymerase/TaKaRa+Ex+Taq+DNA+Polymerase/pmc13090712-41-0-7
Average 98 stars, based on 16023 article reviews
Ex Taq Dna Polymerase, supplied by TaKaRa, used in various techniques. Bioz Stars score: 98/100, based on 16023 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ex+taq+polymerase/TaKaRa+Ex+Taq+DNA+Polymerase/pmc13090712-41-0-7
Average 98 stars, based on 16023 article reviews
ex taq dna polymerase - by Bioz Stars,
2026-10
98/100 stars
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Polymerase Chain Reaction:Article Title: Apple consumption is associated with obesity- and lipid-related parameters and gut microbiota profiles across enterotypes: 12-week single-blind trial in Japanese adults Article Snippet: .. The PCR amplification was performed in a 10 μL reaction mixture containing 1 μL of 10 × Ex buffer (TaKaRa Bio, Otsu, Shiga, Japan), 0.8 μL dNTPs (TaKaRa Bio), 0.5 μL each of the forward and reverse primers, 2 μL template DNA, and 0.1 μL of Article Title: Host regulation of gill microbiota by a mucosal C-type lectin in the kuruma shrimp Penaeus japonicus Article Snippet: Mucosal organs are the primary interface through which shrimp are exposed to environmental microorganisms and pathogens, however, our understanding of crustacean mucosal immunity and its relationship with resident microbiota remains limited.. In this study, we examined the role of a mucosa-specific C-type lectin, MjGCTL, in the regulation of mucosal microbiota and disease susceptibility in kuruma shrimp Penaeus japonicus.. MjGCTL mRNA expression was detected in the gill, stomach, and hindgut, which are recognized as mucosal organs in shrimp. Article Title: Microorganism of Article Snippet: .. For genetic manipulation, Article Title: Compartment-resolved in vivo phage display biopanning reveals constraint-driven peptide sequence landscapes Article Snippet: .. The primer sequences used were: Forward: 5′-TCGTCGGCAGCGTCAGATGTGTATAAGAGACAGttggtgccggcaac-3′ Reverse: 5′-GTCTCGTGGGCTCGGAGATGTGTATAAGAGACAGgccctctatagttagc-3′ PCR reactions were performed using the following reaction mixture: 5 μl PCR buffer, 4 μl dNTP mix, 1 μl each of forward and reverse primers (10 μM), 0.3 μl Article Title: Genome-Scale Phylogenetic Evidence Supports the Synonymy of Lasiodiplodia brasiliensis with Lasiodiplodia theobromae Article Snippet: .. PCR reactions were performed in 10 μL volumes, consisting of 1 μL of 10× Taq buffer, 0.8 μL of dNTPs (2.5 mM each), 0.1 μL of each primer, 0.05 μL of Article Title: Genome-Scale Phylogenetic Evidence Supports the Synonymy of Lasiodiplodia brasiliensis with Lasiodiplodia theobromae Article Snippet: .. PCR reactions were performed in 10 μL volumes, consisting of 1 μL of 10× Taq buffer, 0.8 μL of dNTPs (2.5 mM each), 0.1 μL of each primer, 0.05 μL of Article Title: Evaluation of Predation on Phytophagous Insects by a Phytozoophagous Mirid Bug, Apolygus lucorum . Article Snippet: Primers for A. gossypii: Forward primer MYF: 5′-TTCACATCAGCAACTATAATC-3′ Reverse primer MYR: 5′-ACTACATAATAAGTGTCATGC-3′ Amplicon length: 208 bp. (c) PCR amplification: PCR reactions were performed in a thermal cycler (Bioer, Hangzhou, China). .. Each 25 μL reaction mixture contained 0.25 μL of Amplification:Article Title: Apple consumption is associated with obesity- and lipid-related parameters and gut microbiota profiles across enterotypes: 12-week single-blind trial in Japanese adults Article Snippet: .. The PCR amplification was performed in a 10 μL reaction mixture containing 1 μL of 10 × Ex buffer (TaKaRa Bio, Otsu, Shiga, Japan), 0.8 μL dNTPs (TaKaRa Bio), 0.5 μL each of the forward and reverse primers, 2 μL template DNA, and 0.1 μL of Laser Capture Microdissection:Article Title: Compartment-resolved in vivo phage display biopanning reveals constraint-driven peptide sequence landscapes Article Snippet: .. The primer sequences used were: Forward: 5′-TCGTCGGCAGCGTCAGATGTGTATAAGAGACAGttggtgccggcaac-3′ Reverse: 5′-GTCTCGTGGGCTCGGAGATGTGTATAAGAGACAGgccctctatagttagc-3′ PCR reactions were performed using the following reaction mixture: 5 μl PCR buffer, 4 μl dNTP mix, 1 μl each of forward and reverse primers (10 μM), 0.3 μl Sterility:Article Title: Evaluation of Predation on Phytophagous Insects by a Phytozoophagous Mirid Bug, Apolygus lucorum . Article Snippet: Primers for A. gossypii: Forward primer MYF: 5′-TTCACATCAGCAACTATAATC-3′ Reverse primer MYR: 5′-ACTACATAATAAGTGTCATGC-3′ Amplicon length: 208 bp. (c) PCR amplification: PCR reactions were performed in a thermal cycler (Bioer, Hangzhou, China). .. Each 25 μL reaction mixture contained 0.25 μL of |
