394 dna rna automatic synthesizer (Thermo Fisher)
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394 dna rna automatic synthesizer
394 Dna Rna Automatic Synthesizer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/394+dna+rna+automatic+synthesizer/DNA/10__1134_slash_s1068162024606979-96-6-10
Average 99 stars, based on 1 article reviews
394 Dna Rna Automatic Synthesizer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/394+dna+rna+automatic+synthesizer/DNA/10__1134_slash_s1068162024606979-96-6-10
Average 99 stars, based on 1 article reviews
394 dna rna automatic synthesizer - by Bioz Stars,
2026-09
99/100 stars
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other:Article Title: Species-Level Identification of SARS-CoV-2 by an E Gene Conservative Site Article Snippet: The appearance of mutations in the genes encoding the surface proteins of the new type of coronavirus SARS-CoV-2, when it circulates in the host population, makes it difficult to use monoclonal antibodies for its species identification.. In such cases, the choice of conservative genetic targets allows identification by molecular biological methods.. In this work, previously developed primers specific to the E-gene fragment were tested to detect a new type of coronavirus on six isolates belonging to different genetic variants (the original Wuhan strain, delta and omicron). Article Title: Study of Multiple Enzymatic Incorporation of Modified Nucleotides of Purine and Pyrimidine Nature in the Growing DNA Chain Article Snippet: The substrate properties of nitrogen-base modified derivatives of purine and pyrimidine deoxynucleoside triphosphates during their simultaneous pairwise insertion into the growing DNA strand have been studied.. Modified nucleotides were introduced using real-time PCR and the primer extension reaction; in one reaction, derivatives with both different and similar functional substituents were used.. Genomic bacterial DNA, specially constructed synthetic DNA fragments, and SELEX libraries were used as templates. Synthesized:Article Title: A Method for Increasing the Efficiency of Selection of Aptamers to Cellular Receptors Article Snippet: Objective: A method to increase the efficiency of cell-SELEX-based selection of aptamers to cellular receptors, in particular, to the receptor tyrosine kinase c-KIT, was presented.. Methods: Direct monitoring of each aptamer selection cycle by analyzing the shift of the melting curve towards higher temperatures allows monitoring the enrichment of a combinatorial oligonucleotide library due to the correlation of increasing GC content and melting temperature with an increase of aptamer affinity for the corresponding target.. Results and Discussion: The use of non-ionic surfactants (Tween 20) in the composition of buffer solutions, as well as trypsinolysis of surface proteins at the stage of elution of the oligonucleotide library bound to the cell surface, significantly reduce non-specific sorption. Modification:Article Title: [Synthesis and characteristics of modified DNA fragments containing thymidine glycol residues]. Article Snippet: Chemical synthesis of a series of modified oligodeoxyribonucleotides containing one or two residues of thymidine glycol (5,6-dihydro-5,6-dihydroxythymidine), the main product of oxidative DNA damage, is described.. The thermal stability of DNA duplexes containing thymidine glycol residues was studied using UV spectroscopy.. Introduction of even one thymidine glycol residue into the duplex structure was shown to result in its significant destabilization. |