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Bioer Technology Co Ltd conventional pcr
Conventional Pcr, supplied by Bioer Technology Co Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/conventional+pcr/conventional+instrument+pcr/pm41927739-87-0-4
Average 86 stars, based on 1 article reviews

conventional pcr - by Bioz Stars, 2026-11

86/100 stars

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Article Title: Genetic characterization of Haemaphysalis (Rhipistoma) indica and Haemaphysalis (Segalia) montgomeryi ticks (Ixodoidea: Ixodidae).
Article Snippet: The extracted genomic DNA samples were subjected to conventional PCR (BIOER, China), for the amplification of partial fragments of 12S rDNA, 16S rDNA, cox1, and ITS2.

Article Title: Molecular evidence of Borrelia theileri and closely related Borrelia spp. in hard ticks infesting domestic animals
Article Snippet: All extracted genomic DNA samples were subjected to a conventional PCR (BIOER, China).

Article Title: First report on detection of Hepatozoon ayorgbor in Rhipicephalus haemaphysaloides and Hepatozoon colubri in Haemaphysalis sulcata and Hyalomma anatolicum : risks of spillover of Hepatozoon spp. from wildlife to domestic animals
Article Snippet: For the amplification of 18S rRNA fragments of Hepatozoon spp., the extracted genomic DNA samples were subjected to conventional PCR (BIOER, China) using specific primers: HEP2 144-169-F (5′-GGTAATTCTAGAGCTAATACATGAGC-3′) and HEP2 743-718-R (5′-ACAATAA AGTA AAAAACAYTTCAAAG-3′), and PCR experimental conditions were set as previously described ( ).

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Article Title: New host record of Amblyomma pakhtunensis on the Indian Pangolin (Manis crassicaudata) with detection of a distinct Borrelia lineage.
Article Snippet: .. Conventional PCR (model GE-96G, BIOER, Hangzhou, China) was performed on genomic DNA samples to target partial fragments of the tick 16S rRNA gene, as well as the associated borrelial 16S rRNA, glpQ, and flaB genes (Table 1). .. Tick and borrelia 16S rRNA, Borrelia flaB (first round), and glpQ PCRs were carried out in 20 μL reaction mixture containing 2μL of DNA (~ 50 ng/μL), 1μL of each primer (10 pmol/μL), 4μL of nuclease-free PCR water, and 12μL of DreamTaq green MasterMix (2X) (Thermo Scientific,Waltham, MA, USA).

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