Turbo FISH: A Method for Rapid Single Molecule RNA FISH
Por um escritor misterioso
Last updated 22 novembro 2024
Advances in RNA fluorescence in situ hybridization (RNA FISH) have allowed practitioners to detect individual RNA molecules in single cells via fluorescence microscopy, enabling highly accurate and sensitive quantification of gene expression. However, current methods typically employ hybridization times on the order of 2–16 hours, limiting its potential in applications like rapid diagnostics. We present here a set of conditions for RNA FISH (dubbed Turbo RNA FISH) that allow us to make accurate measurements with no more than 5 minutes of hybridization time and 3 minutes of washing, and show that hybridization times can go as low as 30 seconds while still producing quantifiable images. We further show that rapid hybridization is compatible with our recently developed iceFISH and SNP FISH variants of RNA FISH that enable chromosome and single base discrimination, respectively. Our method is simple and cost effective, and has the potential to dramatically increase the throughput and realm of applicability of RNA FISH.
Using Single Molecule mRNA Fluorescent in Situ Hybridization (RNA-FISH) to Quantify mRNAs in Individual Murine Oocytes and Embryos
IJMS, Free Full-Text
Comparison of fixation conditions for both traditional overnight
RNA Imaging with Multiplexed Error-Robust Fluorescence In Situ Hybridization (MERFISH).
RNA FISH for vision research
PDF] Real-Time Monitoring of Fluorescence in Situ Hybridization Kinetics.
Figure 6 from Turbo FISH: A Method for Rapid Single Molecule RNA FISH
HT-smFISH: a cost-effective and flexible workflow for high-throughput single -molecule RNA imaging
Turbo FISH: A Method for Rapid Single Molecule RNA FISH
FISHing fish - the Node
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Turbo FISH: A Method for Rapid Single Molecule RNA FISH
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Turbo FISH: A Method for Rapid Single Molecule RNA FISH
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