Techniques for buffer exchange (Desalting columns, Dialysis, & Diafiltration): Pros, cons, & going-ons
The 3 D’s of buffer exchange! There are 3 main techniques for buffer exchange of proteins (or nucleic acids): Desalting […]
The 3 D’s of buffer exchange! There are 3 main techniques for buffer exchange of proteins (or nucleic acids): Desalting […]
Part of my goal with some of the work I do is to de-mystify the hidden curriculum aspects of academic […]
Extra note for grad school students: One of the key things to know is that a lot more gets to […]
If you want to know more, I recommend checking out Cytiva’s chromatography handbooks. More on HIC and optimizing it: https://www.cytivalifesciences.com/en/us/insights/optimizing-hydrophobic-interaction-chromatography […]
Proteins don’t have “a” structure – they typically have many; because proteins don’t stay still! Conformational changes (shape-shifts) can come […]
Who’s who in a lab & what do they do? (way overgeneralized); (in academia mainly – makeups, precise roles & […]
Small nucleic acid therapeutics/tools (sometimes referred to as oligonucleotide therapeutics) include aptamers; RNAi-acting small RNAs – microRNA (miRNA) and small interfering […]
We often say we stick the “gene” for making a protein into cells to get them to make the protein […]
Huge thanks to Ivana Radosavljević, immunotherapy scientist, and self-proclaimed science enthusiast for this translation into German!