CRISPR/Cas9 For Photoactivated Localization Microscopy (PALM)

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📝 Original Info

  • Title: CRISPR/Cas9 For Photoactivated Localization Microscopy (PALM)
  • ArXiv ID: 1403.6738
  • Date: 2014-03-27
  • Authors: Researchers from original ArXiv paper

📝 Abstract

We demonstrate that endonuclease deficient Clustered Regularly Interspaced Short Palindromic Repeats CRISPR-associated Cas9 protein (dCas9) fused to the photo-convertible fluorescence protein monomeric mEos3.1 (dCas9-mEos3) can be used to resolve sub-diffraction limited features of repetitive gene elements, thus providing a new route to investigate high-order chromatin organization at these sites.

💡 Deep Analysis

Deep Dive into CRISPR/Cas9 For Photoactivated Localization Microscopy (PALM).

We demonstrate that endonuclease deficient Clustered Regularly Interspaced Short Palindromic Repeats CRISPR-associated Cas9 protein (dCas9) fused to the photo-convertible fluorescence protein monomeric mEos3.1 (dCas9-mEos3) can be used to resolve sub-diffraction limited features of repetitive gene elements, thus providing a new route to investigate high-order chromatin organization at these sites.

📄 Full Content

We demonstrate that endonuclease deficient Clustered Regularly Interspaced Short Palindromic Repeats CRISPR-associated Cas9 protein (dCas9) fused to the photo-convertible fluorescence protein monomeric mEos3.1 (dCas9-mEos3) can be used to resolve sub-diffraction limited features of repetitive gene elements, thus providing a new route to investigate high-order chromatin organization at these sites.

Reference

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