Exploring a peptide nucleic acid-based antisense approach for CD5 targeting in chronic lymphocytic leukemia | PLOS ONE
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How to avoid the formation of traces and dimers in DNA gel electrophoresis? | ResearchGate
SOLVED: Consider the DNA sequence below. Design two 14-base primers to amplify the full length of the sequence. Pay attention to the polarity of each primer. For full points, do not add
SOLVED: 1. Design primers that will amplify the following region of DNA (assume this is one strand from a double stranded region of DNA). The primers should be 15 bases in length.
OligoAnalyzer Tool - Instructions for use | IDT
De novo sequencing and analysis of the transcriptome of two highbush blueberry (Vaccinium corymbosum L.) cultivars 'Bluecrop' and 'Legacy' at harvest and following post-harvest storage | PLOS ONE
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Frontiers | Reverse Transcription Recombinase-Aided Amplification Assay With Lateral Flow Dipstick Assay for Rapid Detection of 2019 Novel Coronavirus
OligoAnalyzer Tool - Instructions for use | IDT
What is a good software to check primer dimer formation and hairpin loop formation? | ResearchGate
PCR Primer Design for Multiplex Assays
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Oligo Analysis Tool
Solved Design two primers that will completely amplify the | Chegg.com
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SorTn-seq: a high-throughput functional genomics approach to discovering regulators of bacterial gene expression | Nature Protocols
Quantifying dominant bacterial genera detected in metagenomic data from fish eggs and larvae using genus‐specific primers - Najafpour - 2022 - MicrobiologyOpen - Wiley Online Library
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