We narrowed to 512 results for: Set
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TypeBlog PostPublishedApril 6, 2021, 12:30 p.m....sample, we’ll then load it on to our new MiSeq and set up the run making sure to note the appropriate barcode...
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CRISPR in the Clinic
TypeBlog PostPublishedNov. 2, 2023, 1:15 p.m....especially for systemic approaches, has its own unique set of obstacles. Thus far, several targeted therapies... -
Corralling and Cornering the Goldilocks Antibody
TypeBlog PostPublishedAug. 9, 2022, 1:15 p.m....happens when the antibody is produced from a new set of animals), and wrong application (different experiments... -
Adeno Associated Virus (AAV) for Cell and Gene Therapy
TypeBlog PostPublishedNov. 7, 2017, 1:59 p.m....profiles have limited their usability in clinical settings. On the other hand, vectors derived from AAV have...the gene RPE65. It is characterized by childhood onset of blindness and was thought to be untreatable until... -
Plasmids 101: Terminators and PolyA signals
TypeBlog PostPublishedMarch 31, 2016, 2:30 p.m....read-through. Chris Voigt’s lab has characterized a set of prokaryotic terminators and deposited several ... -
AAV Vector Quality Control: Going the Extra Mile with NGS
TypeBlog PostPublishedSept. 12, 2017, 1:44 p.m....a large number of hits to one sequence/gene - we set our threshold at >100 hits - immediately raises a... -
Cloning Mammalian Cells with the Agarose Method
TypeBlog PostPublishedSept. 7, 2017, 12:17 p.m....containing serum in each well. A 200 ul pipettor is set to 200 ul, wiped down with 70% ethanol, and a box... -
Which Fluorescent Protein Should I Use?
TypeBlog PostPublishedMay 20, 2014, 2:06 p.m.... brightness is compared to that of EGFP which is set as 1. Some proteins are very dim (e.g. TagRFP657,... -
Capturing a Moment with Marc Zimmer’s “The State of Science”
TypeBlog PostPublishedJuly 30, 2020, 1:15 p.m....future in under 200 pages is an impressive task to set oneself. As a scientist who enjoys learning a little... -
Meet an Addgenie: Insights into Grad School, Career Paths, and More
TypeBlog PostPublishedJune 25, 2020, 1:15 p.m....have the idea that if you don’t get your PhD you’re set up for failure. Listening to Kenkel’s story has helped... -
No Llamas Required - Synthetic Nanobodies Against Membrane Proteins
TypeBlog PostPublishedJune 18, 2020, 1:15 p.m....convex scaffold and are randomized with a defined set of different trinucleotides (corresponding to different... -
Of Myc and Men
TypeBlog PostPublishedJan. 19, 2023, 2:15 p.m.... the same target. In the 1980s, Munro and Pelham set out to address this issue by developing generic strategies... -
A Guide to Starting Your Own Journal Club
TypeBlog PostPublishedFeb. 6, 2020, 3 p.m.... notice for the first meeting so that people can set aside time in their schedules and read the paper ...). This notice can be shortened as the meeting settles in and people get the time recurrently carved out... -
Chromoproteins: Colorful Proteins For Molecular Biology Experiments
TypeBlog PostPublishedFeb. 4, 2020, 2:15 p.m....chromoproteins are actually a subset of the fluorescent protein family. What sets them apart is the way they... -
The Scientific Conference Poster Session: Tips for Success
TypeBlog PostPublishedAug. 29, 2019, 12:50 p.m....list of posters of interest, then you’ve already set yourself up for success. But sometimes, attendees... -
10 Basic tips for mammalian cell culture
TypeBlog PostPublishedJuly 12, 2018, 1:09 p.m.... you identify bacterial and yeast contaminants. Set up a routine to split cells Don’t be lazy about splitting... -
Addgene's Cancer Collection Pages Connect the Research Community
TypeBlog PostPublishedSept. 6, 2016, 2:30 p.m....Pathway Clone Collection 2.0. The collection is a set of vectors for use with the Gateway Cloning Platform... -
Google Forums Round Up: First Impressions of NgAgo
TypeBlog PostPublishedAug. 4, 2016, 2:30 p.m....there include: Google Groups - I've specifically set up a forum where NgAgo users can share protocols ... -
PITChing MMEJ as an Alternative Route for Gene Editing
TypeBlog PostPublishedFeb. 23, 2016, 3:30 p.m....allow for two sets of microhomologies (5’ and 3’) to anneal, knocking the GFP-Puro cassette into the locus...protocol for MMEJ-mediated knock-in of a GFP-Puro cassette into a given locus, just upstream of a stop codon...microhomology to the insertion locus flanking the GFP-Puro cassette. Three double stranded breaks are necessary for...for knock-in: one on either side of the GFP-Puro cassette and one in between the 5’ and 3’ microhomologies...of PITCh. The PITCh plasmid contains a GFP-Puro cassette flanked by 5' and 3' microhomology and PITCh-gRNA...creates two DSBs in the PITCh plasmid to release the cassette, and an insertion-locus-specific gRNA cleaves ...and 3’ microhomologies are added to the GFP-Puro cassette via PCR, and this construct is inserted into the... -
Fluorescent Proteins 101: Fluorescent Protein Timers
TypeBlog PostPublishedMay 4, 2017, 2:30 p.m.... the use of a given timer in many experimental settings. Monomeric fluorescent protein timers Since the... simplifies cloning and makes your experimental setup less cumbersome. 3. Portability across multiple ...