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Titlebook: Nucleic Acid Detection and Structural Investigations; Methods and Protocol Kira Astakhova,Syeda Atia Bukhari Book 2020 Springer Science+Bus

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樓主: Coagulant
31#
發(fā)表于 2025-3-27 00:10:46 | 只看該作者
1064-3745 tection and Structural Investigations: Methods and Protocols .aims present aims to present methodologies combine cutting-edge innovation with sound theory and practical applications in life sciences..978-1-0716-0140-2978-1-0716-0138-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
32#
發(fā)表于 2025-3-27 04:56:02 | 只看該作者
33#
發(fā)表于 2025-3-27 09:06:38 | 只看該作者
Paresh Prajapati,Wang-Xia Wang,Peter T. Nelson,Joe E. Springern engineering litigation and include. Students in forensic engineering and risk engineering will find the book’s cross-displinary approach an ideal introduction to the subject..978-1-84996-553-8978-1-84628-097-9
34#
發(fā)表于 2025-3-27 09:39:54 | 只看該作者
35#
發(fā)表于 2025-3-27 15:14:34 | 只看該作者
36#
發(fā)表于 2025-3-27 19:14:34 | 只看該作者
37#
發(fā)表于 2025-3-28 01:33:14 | 只看該作者
Kira Astakhova,Syeda Atia BukhariIncludes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts
38#
發(fā)表于 2025-3-28 05:04:23 | 只看該作者
Subtyping of Swine Influenza Using a High-Throughput Real-Time PCR Platform and a Single Microfluidi in diagnostic laboratories. Here we describe how automation of PCR reactions using integrated fluidic circuits (IFCs), an IFC controller MX and a Biomark HD instrument allows for the testing of 48 field samples with swine influenza for up to 48 different subtypes simultaneously in nanoliter volumes.
39#
發(fā)表于 2025-3-28 08:13:17 | 只看該作者
5′-Monopyrene and 5′-Bispyrene 2′-O-methyl RNA Probes for Detection of RNA Mismatcheseotides have demonstrated their effectiveness as fluorescent hybridization probes. Here we describe the synthesis, isolation, and analysis of 5′-monopyrene and 5′-bispyrene conjugates of oligo(2′-O-methylribonucleotides) and their application as probes for fluorescent detection of mismatches in RNA targets.
40#
發(fā)表于 2025-3-28 11:58:36 | 只看該作者
Universal Library Preparation Protocol for Efficient High-Throughput Sequencing of Double-Stranded Rfour main steps, viz., enzyme treatment, precipitation using lithium chloride, full-length amplification of cDNAs, and tailing adapters for high-throughput sequencing. This protocol will be useful for all double-stranded RNA viruses and for all of the high-throughput sequencing platforms.
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