first-generation sequencing (Sangon Biotech)
90
Structured Review
Sangon Biotech
first-generation sequencing
First Generation Sequencing, supplied by Sangon Biotech, 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/first-generation+sequencing/first+generation+sequencing/pmc11729505-50-16-11
Average 90 stars, based on 1 article reviews
First Generation Sequencing, supplied by Sangon Biotech, 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/first-generation+sequencing/first+generation+sequencing/pmc11729505-50-16-11
Average 90 stars, based on 1 article reviews
first-generation sequencing - by Bioz Stars,
2026-10
90/100 stars
Images
Related Articles
other:Article Title: Diversity of classic and novel human astrovirus in outpatient children with acute gastroenteritis in Shanghai, China Article Snippet: All amplification products of HAstV were subjected to sequencing using Article Title: Effectiveness of Pentavalent Rotavirus Vaccine in Shanghai, China: A Test-Negative Design Study. Article Snippet: Objective To evaluate vaccine effectiveness (VE) of a live oral pentavalent rotavirus vaccine (RotaTeq, RV5) among young children in Shanghai, China, via a test-negative design study.. Study design We consecutively recruited children visiting a tertiary children’s hospital for acute diarrhea from November 2021 to February 2022.. Information on clinical data and rotavirus vaccination was collected. Article Title: An ultrasensitive DNA-enhanced amplification method for detecting cfDNA drug-resistant mutations in non-small cell lung cancer with selective FEN-assisted degradation of dominant somatic fragments. Article Snippet: Objectives: Blood cell-free DNA (cfDNA) can be a new reliable tool for detecting epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer (NSCLC) patients.. However, the currently reported cfDNA assays have a limited role in detecting drug-resistant mutations due to their deficiencies in sensitivity, stability, ormutation detection rate.. Methods: We developed an Archaeoglobus fulgidus-derived flap endonuclease (Afu FEN)-based DNA-enhanced amplification systemofmutated cfDNAbydesigning a pair of hairpin probes to anneal with wild-type cfDNA to form two 5′-flaps, allowing for the specific cleavage of wild-type cfDNA by Afu FEN.When the dominant wild-type somatic cfDNA fragments were cleaved by structure-recognition-specific Afu FEN, the proportion of mutated cfDNA in the reaction system was greatly enriched. Article Title: Role of transcription factor complex OsbHLH156-OsIRO2 in regulating manganese, copper, and zinc transporters in rice. Article Snippet: Iron (Fe), manganese (Mn), copper (Cu), and zinc (Zn) are essential micronutrients that are necessary for plant growth and development, but can be toxic at supra-optimal levels.. Plants have evolved a complex homeostasis network that includes uptake, transport, and storage of these metals.. It was shown that the transcription factor (TF) complex OsbHLH156–OsIRO2 is activated under Fe deficient conditions and acts as a central regulator on Strategy II Fe acquisition. Article Title: Newborn ornithine carbamyltransferase deficiency caused by new OTC gene mutations: a report of two cases and review of the literature on phenotype and genotype Article Snippet: Basic Research Program from Shenzhen Science and Techno1ogy Innovation Commission (JCYJ20180228175137465); the TaKaRa Ex Taq Hot Start kit of Dalian Bao Biological Co., Ltd.(Dalian, China), NO Payments; the Polymerase Chain Reaction:Article Title: Predictive Application Value of Metagenomic Next-Generation Sequencing in the Resistance of Carbapenem-Resistant Enterobacteriaceae Article Snippet: The PCR amplification conditions were as follows: initial denaturation at 94°C for 3 min, followed by 35 cycles, each consisting of denaturation at 94°C for 1 min, annealing at 55°C for 1 min, and extension at 72°C for 2 min, with a final extension at 70°C for 5 min. After agarose gel electrophoresis of the PCR products, the bands were observed using an imaging system and compared with DNA Ladder H1 (100–1000 bp; Sangon Biotech, China; Cat# B500343) to determine their size. .. For positive samples, the original PCR amplification products were sent to Sangon Biotech Co., Ltd., for Amplification:Article Title: Predictive Application Value of Metagenomic Next-Generation Sequencing in the Resistance of Carbapenem-Resistant Enterobacteriaceae Article Snippet: The PCR amplification conditions were as follows: initial denaturation at 94°C for 3 min, followed by 35 cycles, each consisting of denaturation at 94°C for 1 min, annealing at 55°C for 1 min, and extension at 72°C for 2 min, with a final extension at 70°C for 5 min. After agarose gel electrophoresis of the PCR products, the bands were observed using an imaging system and compared with DNA Ladder H1 (100–1000 bp; Sangon Biotech, China; Cat# B500343) to determine their size. .. For positive samples, the original PCR amplification products were sent to Sangon Biotech Co., Ltd., for Sequencing:Article Title: Predictive Application Value of Metagenomic Next-Generation Sequencing in the Resistance of Carbapenem-Resistant Enterobacteriaceae Article Snippet: The PCR amplification conditions were as follows: initial denaturation at 94°C for 3 min, followed by 35 cycles, each consisting of denaturation at 94°C for 1 min, annealing at 55°C for 1 min, and extension at 72°C for 2 min, with a final extension at 70°C for 5 min. After agarose gel electrophoresis of the PCR products, the bands were observed using an imaging system and compared with DNA Ladder H1 (100–1000 bp; Sangon Biotech, China; Cat# B500343) to determine their size. .. For positive samples, the original PCR amplification products were sent to Sangon Biotech Co., Ltd., for Article Title: Comparison of TLR4 Genotype and TLR4 Pathway-Related Cytokines in Different Strains of Mice in Response to Pertussis Toxin Challenge Article Snippet: The amplification process was performed on Applied Biosystems (ABI) as follows: 94 °C 5 min; 30 cycles of 94 °C 30 s, 30 s at optimized annealing temperature, and 30 s at 72 °C; and finally 7 min at 72 °C. .. The harvested fragments were then subjected to |