Cargando…
mScarlet and split fluorophore mScarlet resources for plasmid-based CRISPR/Cas9 knock-in in C. elegans
Fluorescent proteins allow the expression of a gene and the behavior of its protein product to be observed in living animals. The ability to create endogenous fluorescent protein tags via CRISPR genome engineering has revolutionized the authenticity of this expression, and mScarlet is currently our...
Autores principales: | Witten, Gillian, DeMott, Ella, Huang, George, Zelasko, Francis, de Jesus, Bailey, Mulchand, Chandi, Schuck, Liam, Pullman, Stephen, Perez, Amelie, Mahableshwarkar, Priya, Wu, Zheng, Cardona, Eric Andrew, Pierce, Jonathan T, Dickinson, Daniel J, Doonan, Ryan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Caltech Library
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308244/ https://www.ncbi.nlm.nih.gov/pubmed/37396790 http://dx.doi.org/10.17912/micropub.biology.000871 |
Ejemplares similares
-
An
nhr-23::mScarlet::3xMyc
knock-in
allele for studying spermatogenesis and molting
por: Myles, Krista M., et al.
Publicado: (2023) -
Polyglutamine toxicity assays highlight the advantages of mScarlet for imaging in
Saccharomyces cerevisiae
por: Albakri, Maram B., et al.
Publicado: (2018) -
RedEfish: Generation of the Polycistronic mScarlet: GSG-T2A: Ttpa Zebrafish Line
por: Head, Brian, et al.
Publicado: (2021) -
Comparing the performance of mScarlet-I, mRuby3, and mCherry as FRET acceptors for mNeonGreen
por: McCullock, Tyler W., et al.
Publicado: (2020) -
Fluorescent hiPSC-derived MYH6-mScarlet cardiomyocytes for real-time tracking, imaging, and cardiotoxicity assays
por: Maria Cherian, Reeja, et al.
Publicado: (2022)