We narrowed to 504 results for: CIT
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TypeBlog PostPublishedOct. 19, 2021, 1:15 p.m....structure, which means each IgM molecule has a binding capacity or valency of 10 antigens. An extra constant domain...
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Viral Vectors 101: Biosensors
TypeBlog PostPublishedJuly 6, 2023, 1 p.m....specifically in their favorite neurons. This specificity is feasible partially because of viruses—keep... -
GCE4All: Making Genetic Code Expansion Accessible
TypeBlog PostPublishedJune 15, 2023, 1:15 p.m....ncAA protocol, to optimize and share, they’re soliciting feedback from scientists on which protocols would... -
Viral Vectors 101: Gamma-Retroviral Packaging Systems
TypeBlog PostPublishedAug. 6, 2024, 1:15 p.m.... of a retroviral provirus (see below). Cloning capacity between the LTRs is ∼8.5 kb, but inserts bigger... -
From Lab Bench to Leadership: Transitioning into Management as a PhD
TypeBlog PostPublishedJan. 21, 2025, 2:15 p.m....the leap into management, the journey can be as exciting as it is challenging. How do you prepare for... -
How Addgene Creates Content
TypeBlog PostPublishedNov. 17, 2022, 2:15 p.m.... in BioRender or use appropriately licensed and cited figures from papers or image sharing repositories... -
Plasmids 101: Screens vs. Selections
TypeBlog PostPublishedNov. 10, 2022, 2:15 p.m....genes are assayed for their role in a particular capacity. Drug screens, on the other hand, are often performed... -
Developing a cold tolerant E. coli using specialized chaperones
TypeBlog PostPublishedJan. 28, 2020, 2:35 p.m....SynBio arena this year with a fresh team of twenty excited undergrads. Team IISER-B’s idea for the iGEM 2019... -
Opto-Nanobodies: Using Light to Manipulate Cell Signaling and Protein Purification
TypeBlog PostPublishedNov. 19, 2019, 2:08 p.m....control of signaling pathways. This is particularly exciting because using light to control signaling provides... -
A Deep Dive into BioBuilder
TypeBlog PostPublishedOct. 11, 2017, 1:44 p.m....create a program that would capitalize on the excitement found through experiential learning. “Students... -
Protein Tagging with CRISPR/Cas9: A Conversation with Mendenhall and Myers
TypeBlog PostPublishedJuly 28, 2015, 2:30 p.m....Spring Harbor in March. A number of groups were excited and asked for the protocol. Since the Addgene page... -
3 Challenges in Plant Synthetic Biology
TypeBlog PostPublishedJuly 22, 2014, 5:46 p.m....the repository, MoClo and GreenGate, and we are excited to see how this exchange of genetic tools facilitates... -
Hot Plasmids April 2018 - Protein Degradation, Nanoscopy, FIRE-Cas9, and Yeast Expression Tools
TypeBlog PostPublishedApril 23, 2018, 2 p.m....results to rapamycin inhibition. To assess TRIM21 toxicity, Clift et al. created stable cell lines overexpressing... -
Visualizing Protein Turnover In Situ
TypeBlog PostPublishedJan. 16, 2018, 3:20 p.m....specific endogenous proteins in any cell type. Exciting! Many thanks to our guest blogger, Eugenia Rojas... -
Choosing the B(right)est Fluorescent Protein: Aggregation Tendency
TypeBlog PostPublishedJune 15, 2017, 2:30 p.m.... the aforementioned methods only determine the capacity of homodimerization in aqueous solution. In cyto... -
Plasmids 101: CcdB - The Toxic Key to Efficient Cloning
TypeBlog PostPublishedDec. 8, 2016, 3:30 p.m....through the loss of the F plasmid, succumb to the toxicity of CcdB. Figure 1: Image from Bernard... -
Summer SciComm: Preprints
TypeBlog PostPublishedAug. 16, 2022, 1:15 p.m.... scientific communication needs. The most often-cited reasons researchers might not post a preprint are... -
What's New in CRISPR - November 2021
TypeBlog PostPublishedNov. 18, 2021, 2:15 p.m.... Holmes Several labs have recently shared some exciting plasmid tools to optimize prime editing systems... -
Antibodies 101: Fab Fragments
TypeBlog PostPublishedSept. 5, 2024, 1:15 p.m....when used in structural studies and reduces immunogenicity when used in vivo. Of course, the lack ... -
The time and cost required to make a plasmid
TypeBlog PostPublishedMarch 23, 2023, 1:15 p.m....finally dive deep into generating the data you’re excited about. When we were closing in on the one million...