More posts in DECODED

• Scale and yield—Are they the same?
• Genome editing: Isolating clones for genotypic and phenotypic characterization
• A mutant <em> A.s. </em> Cas12a (Cpf1) for CRISPR genome editing shows broad temperature tolerance and a high ratio of on:off target activity, with site-to-site reliability rivaling <em>S.p.</em> Cas9
• High-fidelity Cas9 provides highly efficient genome editing with reduced off-target effects, even in primary cells
• Viral surveillance using wastewater
• Analyze your CRISPR genome edits with IDT's cloud-based software
• Multiplexed targeted next generation sequencing coverage
• Prime editing with pegRNA: a novel and precise CRISPR genome editing system
• Applications and benefits of CRISPR functional genomics screens using arrayed guide RNA libraries
• Protocols for CRISPR genome editing in your model system
• Using CRISPR-Cas9 technology for targeted nanopore sequencing
• <em>The CRISPR Basics Handbook</em>: An IDT publication to help you learn CRISPR
• SHERLOCK, PAC-MAN, and more: How CRISPR-Cas13 enzymes may be useful in the COVID-19 pandemic and beyond
• Design functional oligos with poly G runs
• Alt-R™ HDR Donor Blocks can enable long DNA knock-ins while decreasing undesired edits
• Cloning strategies: Cohesive end cloning
• SUN™ fluorophore
• PrimeTime One-Step 4X Broad-Range Master Mix for one-step RT-qPCR experiments
• Tips for working with IDT Gene Fragments
• Genome Oligopaint: Painting a clearer picture with oPools™ Oligo Pools

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