We narrowed to 545 results for: SEC
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TypeBlog Post...of CRISPR overall. Type I systems degrade large sections of DNA thanks to the dual action power of Cas3...
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Special Delivery: Fluorophore Targeting for FRET Studies
TypeBlog Post...can transfer energy directly via resonance to the second fluorophore (the acceptor) if the two probes are... -
Affinity Purification of Recombinant Antibodies with Protein A or Protein G
TypeProtocol...Aliquot and freeze upright at -20 °C Procedure Section 1: Affinity chromatography Equilibrate filtered... when purifying the same recombinant antibody. Section 2: Buffer exchange Choose Option 1 or Option 2 ... -
Selecting Your Plasmid Purification Kit
TypeBlog Post...kit. Do you want eco-friendly options? It’s no secret that labs produce a lot of waste. If you are looking... -
CRISPR 101: Cytosine Transversion Editors
TypeBlog Post.... ABE Adenine Base Editor Converts A → G; the second type of base editor invented. CGBE C → G Base... -
CRISPR 101: Multiplex Expression of gRNAs
TypeBlog Post...first gRNA using restriction enzyme BbsI and the second gRNA using restriction enzyme BsaI. If you’re working... -
Prime Editing: Adding Precision and Flexibility to CRISPR Editing
TypeBlog Post...Higher efficiency ✓ ✓ ✓ ✓ ✓ ✓ Second sgRNA to guide nicking of the unedited strand ... -
Optogenetics Guide
TypeGuide...periods. These can range from msec (hChR2) to “long lasting,” e.g. seconds to minutes with stable step-...Zhang F, Bamberg E, Nagel G, Deisseroth K. 2005. Millisecond-timescale, genetically targeted optical control... -
CRISPR Library Amplification
TypeProtocol...add 10 µL of the pool to 990 µL LB then perform a second and then third 1:100 dilution). Plate 100 µL of...not present on the most dilute plate, count the second plate (ie. the 1:10,000 dilution). After 12-18 ... -
Delivery Methods for Generating iPSCs
TypeBlog Post...vectors are better suited for these situations. The second scenario requires higher levels of safety and as... -
CRISPR Guide
TypeGuide...CRISPR in your own research. CRISPR Basics In this section, we will introduce the basic mechanisms of CRISPR...Generating a Knockout Using CRISPR Cas9 undergoes a second conformational change upon target binding. In this...have been developed, including editors based on a second ADAR variant that displays improved specificity...Oost, J. (2012). CRISPR immunity relies on the consecutive binding and degradation of negatively supercoiled... -
Adeno-associated virus (AAV) Guide
TypeGuide...cell lines, such as HeLa and A549 cells, and even insect Sf9 cells , have also been developed. The newly...number indicates the serotype of the genome and the second number the serotype of the capsid. Pseudotyped ... splice donor sequence at its 3' end, while the second vector carries the 3' portion of the gene with ... -
CRISPR Methods for Bacteria: Genome Engineering, CRISPRa, CRISPRi, Base Editing, and More
TypeBlog Post...in this way. As described in the above CRISPRi section, the Marraffini Lab published a robust tool for... -
15 Hot Plasmids from 2017
TypeBlog Post...telomeric DNA), which accumulates when T-loops (secondary telomeric structures) are deleted. Reduction in... -
Addgene's eBook Collection
TypeGuide...101 July 2024 | Second Edition About Viral Vectors 101 July 2024 | Second Edition About This guide... -
Protocol - pLKO.1 – TRC Cloning Vector
TypeProtocol...digestion with EcoRI and AgeI. The oligos from section B contain the shRNA sequence flanked by sequences...polymerase has difficulty reading through the secondary structure of the hairpin sequence. Back to Top... -
Cloning
TypeGuide...preserve the directionality of the cloning reaction. Second, the restriction site is encoded on both the insert... DNA that ends in sequences that form complex secondary structues. You can view an example of a LIC protocol... -
DNA Quantification
TypeProtocol...despite the accuracy of the NanoDrop, if two consecutive samples have significantly different concentrations... -
Protocol - How to Design Primers
TypeProtocol... be relatively simple and contain no internal secondary structure to avoid internal folding. One also ... -
Lab Safety for Biosafety Levels One and Two
TypeProtocol...impenetrable by a needle, and must be able to close securely. Biohazard signs should be placed in all areas...