CLARiTY UV/Vis Spectrophotometers
CLARiTY is power.
CLARiTY is achieving a broader perspective.
CLARiTY is You deciding on the sample
CLARiTY: Measure the sample that matters the most. The choice of clear
or scattering is in your hands.
All of your experience tells you this makes no sense. But your experience is with spectrophotometers that use a cuvette.
CLARiTY models use a DSPC, a ‘DeSa Suspension Presentation Chamber,’ a novel sample holder which includes a quartz integrating cavity packed in a highly reflective chamber.
The only means of light entering the DSPC is through an inlet port; the only means of light exiting the DSPC is through the outlet port and detector. “Scatter” – light which enters the cuvette but scatters 360° rather than straight into the detector – cannot happen.
Achieving a broader perspective:
Think about it: a clear solution can be very limiting.
You might consider this unavoidable and/or of minimal consequence. If so, you stay with our spectrophotometers for clear solutions; we make many!
But! If you care to make measurements of protein in their membrane, or nanoparticles in suspension, or intact tissue, or any other non-clear sample, the CLARiTY is your answer.
With CLARiTY, you are no longer required to distance yourself from the sample – and thus from the results – that would be your first choice if scatter didn’t matter to the spectrophotometer.
Frees you:
You are freed to study exactly the sample in exactly the environment of primary value. And! You are freed from the talent, time, resources, and expense of changing the sample of interest to a clear subset that a cuvette spectrometer demands.
Best Results. Least Waste
Power:
With CLARiTY, you can do work like this: In Situ Capture of the Changing Electron Transport Chain (ETC) Using UV-vis Absorbance Spectrophotometry and other work shared on https://olisclarity.com/research and https://olisclarity.com/experiments
The OLIS CLARiTY: Measure where it matters the most,
whether in solution or suspension!
Obtaining absorbance spectra from turbid retinal cell and tissue suspensions -
Beating the light-scatter problem
Although a powerful analytical tool, spectroscopy is often limited by the nature of the specimen. Spectroscopy typically requires samples to be transparent solutions free of insoluble material, which through light scatter, diffuse the incoming light beam. Although spectroscopy works wonderfully in many areas of biochemistry, such specimen requirements are frequently not possible in cellular or tissue physiological chemistry. Here, molecules work within intracellular, extracellular or membrane …
The CLARiTY Advantage
Integrating Cavity Spectrophotometers For a Powerful New Generation of Measurements
Everyone knows about spectrophotometers that use cuvettes. With cuvette spectrophotometers, accurate results are possible only with perfectly clear samples. When the sample is hazy or turbid, the light beam carrying the absorbance information is scattered, much of it away from the detector. The answer is therefore higher absorbance than is correct. Read more...
The Short and Long of It.
The Short
A single page piece, circa 2014, on using CLARiTY to follow metabolism in the electron transport chain:
“Today, research using a new integrating cavity spectrometer has demonstrated that isolated cell components do not act the same as when those components are in their native environment … when they are not in the environment in which they were designed to function, they may behave differently.”
The Long
A 16 page chapter, circa 2020, on using CLARiTY:
“One thing is certain: one way to understand how a protein functions in an intact organism is to actually observe that protein as it functions in the intact organism. This paper provides an example of just such an observation.”
Having fun demonstrating an early version of a CLARiTY system:
You achieve a beginner’s mind by dropping all expectations and preconceived ideas—shutting off autopilot—and seeing things with an open mind and fresh eyes—like a beginner, like a child.
Beginner’s mind or Shoshin has proven to be a great tool for my professional, creative, and personal life. I stumbled upon this concept when I was learning to meditate.
An integrating cavity can be thought of as a filled integrating sphere. It was the 1950s when group of oceanographers gave this idea a try. Their goal was to achieve a very long pathlength and thus very high sensitivity.