We narrowed to 11 results for: Superfolder GFP

SunTag amplifies fluorescent signals by recruiting multiple copies of GFP. SunTag can help you turn up the brightness in your fluorescent imaging experiments.

Use blue light to control gene expression from PBAD promoters. It's more spatially and temporally precise compared to AraC based expression vectors.

Tips to help you choose which fluorescent protein to use in your experiments.

Cas13a is an RNA cleaving enzyme that can be used to detect specific RNAs. Learn about this and other applications, like nucleic acid detection.

Fluorescent proteins can mis-fold or form aggregates outside of the cytoplasm leading to errors in localization. Avoid these issues with new mOX-FPs.

REPAIR and RESCUE are two CRISPR tools for RNA editing based on Cas13b.

FlipGFP is a genetically encoded caspase reporter that contains a flipped beta strand of GFP. There is no fluorescence unless the caspase cuts the cleavage site between the strands.

Explore empty plasmid backbones with different fluorescent tags to create fusion proteins with your gene of interest.

Many commonly used fluorescent proteins form dimers producing artifacts in a variety of experimental settings. Learn how to avoid these artifacts.

Find plasmids encoding fluorescent biosensors to measure biomolecules or genes via FRET or other assays.

Aptamers are nucleic acid oligos that bind to small molecules to induce their fluorescence and can be used to study RNA localization and dynamics.