Genomics - Flexible Methods for Long-Read RNA Sequencing
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    KeysightFlexible Methods for Long-Read RNA Sequencing
 
RNA analysis has become a vital tool for researchers looking for insight into the study of living things, revealing details about the dynamics of the transcriptome, from single cells to whole tissues.
 
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    KeysightImproving the Magnetic Separation of Biomolecules
 
Isolation and purification of biomolecules (single- and double- stranded DNA, proteins, mRNAs, miRNA, total RNAs), as well as specific organs and cells facilitate a broad range of downstream applications including cloning, gene and protein expression studies, protein-protein interactions, transfection, clinical diagnostics, immunology, PCR and qPCR, cDNA library synthesis, Sanger and NGS sequencing.
 
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 Nanoparticles used to deliver CRISPR gene editing tools into the cell
 
Nanoparticles used to deliver CRISPR gene editing tools into the cellResearchers from Tufts University and the Chinese Academy of Sciences have developed a novel method to effectively deliver the CRISPR/Cas9 (clustered regularly interspaced short palindromic repeat (CRISPR) associated protein 9) gene editing tools into the liver for genetic studies.
 
 
 Research sheds light on sun-induced DNA damage and repair
 
Research sheds light on sun-induced DNA damage and repairIt is a well known fact that the sun’s ultraviolet rays can damage the skin. Now, a new study sheds light on what happens after DNA damage occurs, and how the body initiates repair.
 
 
 Gene modulation goes wireless hacking the "boss gene"
 
Gene modulation goes wireless hacking the "boss gene"Researchers from the University at Buffalo have successfully used technology to wirelessly tweak the functioning of a gene FGFR1. This gene is vital in the growth of embryos into adults. Their experiments were successful in the lab grown brain tissues and shows potential in therapeutics.
 
 
 New CRISPR tool enhances RNA editing
 
New CRISPR tool enhances RNA editingCRISPR-based tools helped revolutionize the ability to target genetic mutations linked to disease development. Such tools focus on using the enzymes Cas9 and Cas12 to target DNA, and Cas13 to target RNA. Now, scientists used a new CRISPR platform that expands the capabilities of RNA editing.
 
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