Whole-mount in situ hybridization (WISH) is an indispensable technique for visualizing spatio-temporal gene expression patterns during the complex process of tissue regeneration.
Nonspecific probe binding is a critical challenge that compromises the accuracy and reliability of hybridization-based techniques essential to genomics, diagnostics, and drug development.
This article provides a systematic framework for researchers and drug development professionals to maximize the signal-to-noise ratio (SNR) in Fluorescence in situ Hybridization (FISH) experiments.
This article provides a systematic analysis of the factors contributing to background staining in whole-mount in situ hybridization (WISH), a critical challenge for researchers and drug development professionals.
High background staining is a common and frustrating challenge in whole-mount in situ hybridization (WISH) that can obscure genuine gene expression signals.
Background noise and autofluorescence present significant challenges for achieving clear, reliable results in embryo in situ hybridization (ISH), impacting data accuracy in developmental biology, drug research, and diagnostics.
This comprehensive review synthesizes current methodologies for enhancing homology-directed repair (HDR) rates in zebrafish knock-in experiments, addressing a critical bottleneck in precision genome editing.
This article provides a comprehensive comparative analysis of two prominent indel detection methods, ICE (Inference of CRISPR Edits) and CRISPR-STAT (Somatic Tissue Activity Test).
This article provides a comprehensive analysis for researchers and drug development professionals on the critical choice between delivering the CRISPR-Cas9 system as a pre-complexed protein (RNP) or as mRNA.
This article details the transformative methodology of multi-locus targeting using synthetic guide RNAs (gRNAs) in zebrafish, a technique that enables highly efficient, biallelic gene knockouts directly in the F0 generation.