When your day-to-day work consists of lots of document editing, you know that every document format needs its own approach and often particular applications. Handling a seemingly simple OSHEET file can often grind the whole process to a stop, especially if you are trying to edit with inadequate tools. To prevent this kind of difficulties, get an editor that will cover all your needs regardless of the file extension and correct light in OSHEET with no roadblocks.
With DocHub, you will work with an editing multitool for virtually any occasion or document type. Minimize the time you used to devote to navigating your old software’s functionality and learn from our intuitive interface while you do the work. DocHub is a sleek online editing platform that handles all your document processing needs for any file, including OSHEET. Open it and go straight to efficiency; no prior training or reading instructions is required to enjoy the benefits DocHub brings to papers management processing. Start by taking a few minutes to create your account now.
See improvements within your papers processing just after you open your DocHub account. Save time on editing with our single solution that will help you become more productive with any document format with which you have to work.
hi guys this is Dan croucher field application specialist with photo metrics and today Im going to talk about light sheet microscopy so firstly lets set out what the challenges are of conventional light microscopy so we know what we need from a microscope life is full of dynamic processes so in order to visualize them we need to image live cells or organisms so the first thing we want to do is avoid photobleaching of photo damage to live samples so we can be sure that the processes were following occur in healthy living cells we also want to capture these dynamic processes in three dimensions because things dont happen just in a single focal plane samples arent all the same size so we need to be able to image varied sample sizes as well as image them from various viewing positions finally we want to minimize out of focus for essence for good optical sectioning the problem is that conventional microscopy on coverslips isnt so compatible with live samples theres no way we can squ
