We narrowed to 275 results for: mel
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TypeBlog Post...2009). If the fluorescence from your target is extremely bright, then the noise likely will not interfere...
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Generating Mouse Models Using CRISPR/Cas9
TypeBlog Post...mouse gene-targeting field. Mice have long been extremely useful in the lab – they are relatively small ... -
Trimmer Lab NeuroMab Collection
TypeCollection...2020. Development, Screening, and Validation of Camelid-Derived Nanobodies for Neuroscience Research. Curr... -
Important Considerations When Using AAVs
TypeBlog Post...1740-1743. PubMed PMID: 17882145. 2. Zincarelli, Carmela, et al. "Analysis of AAV serotypes 1–9 mediated... -
With an Eye Towards the Future, We Look Back at the March for Science
TypeBlog Post...anti-science activists. However, I must say that I was supremely proud of Nashville that morning. Despite the rain... -
Special Delivery: Fluorophore Targeting for FRET Studies
TypeBlog Post...quantitative Ca2+ measurements using improved cameleons." Proceedings of the National Academy of Sciences... -
Molecular Biology Reference
TypeGuide...may cause certain diseases. Sequencing DNA is extremely important when verifying plasmids to ensure each...only sequence short pieces of DNA. This is not extremely useful when trying to sequence an entire plasmid... -
Optogenetics + CRISPR, Using Light to Control Genome Editing
TypeBlog Post...S, Bietz A, Waldhauer MC, Börner K, Fakhiri J, Schmelas C, Dietz L, Grimm D, Correia BE, Eils R, Niopek... -
CRISPR Methods for Bacteria: Genome Engineering, CRISPRa, CRISPRi, Base Editing, and More
TypeBlog Post... E. coli, the system was used successfully in Tatumella citrea, another species of Enterobacteriaceae,... -
CRISPR Guide
TypeGuide...A., Waldhauer, M. C., Börner, K., Fakhiri, J., Schmelas, C., Dietz, L., Grimm, D., Correia, B. E., Eils...Adriaens, C., Ramadoss, G. N., Shi, Q., Hung, K. L., Samelson, A. J., Pogson, A. N., Kim, J. Y., Chung, A., ... -
Viral Vectors 101: Systemic Capsids
TypeBlog Post...doi.org/10.1016/j.neuron.2021.03.011 Hanlon, K. S., Meltzer, J. C., Buzhdygan, T., Cheng, M. J., Sena-Esteves... -
Adeno-associated virus (AAV) Guide
TypeGuide...occurring replication-competent rAAV vectors is extremely reduced by dividing the viral genome between the... -
Antibody Guide
TypeGuide...kD single heavy domain fragments derived from a camelid antibody called a heavy chain antibody (HCAb). ... -
AAV Titration by qPCR Using SYBR Green Technology
TypeProtocol... 2019 Estimate of time required: ~3 h Workflow Timeline Plate set-up: 2 h qPCR run: 1.5 h Data analysis...°C 30 sec / read plate/ repeat 39x from step 3 / melt curve Example of plate set-up: 1 2 3 4 5 6 7 8 A...accurately determine differences between samples. Melt curve analysis: a single peak should be seen. The... -
What is Polymerase Chain Reaction (PCR)
TypeProtocol...Set annealing temperature 5°C below the primer melting temperature (Tm). Set extension step at 1-2 minutes... 3’ primers should be designed to have similar melting temperatures (Tm). Set the annealing temperature... -
Protocol - pLKO.1 – TRC Cloning Vector
TypeProtocol... Qiaquick gel extraction kit Qiagen #28704 Low melting point agarose Sigma #A9414 Luria Broth Agar (LB...37°C for 2 hours. Run digested DNA on 0.8% low melting point agarose gel until you can distinctly see ... -
Protocol - How to Design Primers
TypeProtocol...60% G/C content Start and end with 1-2 G/C pairs Melting temperature (Tm) of 50-60°C Primer pairs should... -
Ligation Independent Cloning
TypeProtocol...Use web-based primer design software to ensure a melting temperature between 50-60°C for your PCR primers... -
Fluorescence Titering Assay
TypeProtocol... institution’s biosafety regulations. Workflow Timeline Day 0: Seed 293T cells Day 1: Transduce cells ... -
General Transfection
TypeProtocol... and different transfection reagents. Workflow Timeline Day 0: Seed HEK293T cells (or a subclone of HEK293T...