Processing
More posts in DECODED
- Oligo modifications that block nuclease degradation
- CRISPR fluorescent <i>in situ</i> hybridization in live cells: a new approach to monitoring chromosomal activities
- Explaining multiple peaks in qPCR melt curve analysis
- Use of Template Switching Oligos (TS Oligos, TSOs) for efficient cDNA library construction
- Antigen-specific B cell enrichment for faster, more efficient antibody discovery
- Photo-cleavable spacer
- Four tips for oligonucleotide quantification with Thermo Scientific™ NanoDrop™ instruments
- 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
- 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
- What is CRISPR screening?
- 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
- Stability of CRISPR reagents under different freezing, storage, and thawing conditions