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.
CLARiTY: Permitting you to Measure Where it Matters the Most, in Solution & Suspension.
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OLIS CLARiTY VF
The perfect instrument for many sample types: organic, inorganic, biological, materials, and more.
Factory configured for UV, Vis, or both
Specify absorbance or fluorescence configuration, which can be changed between measurements
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OLIS CLARiTY 1000
Do you have dreams of understanding metabolism & other kinetic studies within whole cells, living tissue, and more? This is the spectrophotometer you would have designed.
Up to 100 scans per second over 50, 230, or 500 nm span
Brilliant light throughput with highest sensitivity 240-800 nm, easily covering the entire electron transport region and more.
Easily converts for stopped-flow spectroscopy (becoming an OLIS RSM 1000)
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OLIS CLARiTY 17
Choose when you want both CLARiTY studies 240-800 nm and cuvette measurements 185-2600 nm
Built upon an upcycled Cary 14/17, yours or ours
Convertible to UV/Vis/NIR circular dichroism (see OLIS DSM 17)
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OLIS CLARiTY 245
Ideal for live cells to nanoparticles
High-performance scanning Uv/Vis spectrophotometer which is equally an absorbance and fluorescence system.
240-800 nm
Convertible to UV/Vis circular dichroism and CPL (OLIS DSM 245)
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OLIS CLARiTY 1, 2, 3
Perfect for Abs/cm & SRM measurement on hazy samples
Includes the 1, 2, or 3 wavelengths you need
Answer is returned in 4 seconds
Clarifying the sample is 100% optional
Saves waste & expense of clarifying the sample
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Which CLARiTY Should You Choose?
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
Visit our Experiments page to see more applications for the CLARiTY.
CLARiTY: Freedom from the limitation of cuvettes, expanding your choices from sample volume and concentration to solvents.
“Obtaining absorbance spectra from turbid retinal cell and tissue suspensions”
From this powerful article, a few lines: “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. …spectroscopy works wonderfully in many areas of biochemistry, [but] such specimen requirements are frequently not possible in cellular or tissue physiological chemistry [where] molecules work within intracellular, extracellular, or membrane environments.”
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.
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:
CLARiTY F.A.Q.s
Are the results from a cuvette and the CLARiTY integrating cavity the same?
Yes, if there is zero scatter from the sample, both methods return the same results.
No, if the sample scatters light, CLARiTY returns the correct absorbance, while a cuvette system returns extinction.
I don’t want to dilute my sample. What’s the alternative?
Reduce the pathlength, as you would with a traditional cuvette spectrophotometer. CLARiTY instruments can be fitted with integrating cavities of various volumes, from the standard 8 mL to a few microliters. Shorter pathlengths require more concentrated samples.
What is the dynamic range for measuring absorbance?
Approximately 10⁻⁴ AU/cm with the 8 mL integrating cavity and 100 AU/cm with the 0.08 mL flow-through integrating cavity.
Should I use the filled DSPC, a test tube, or a flow-through cell with CLARiTY?
Filled DSPC (8 mL cavity): Provides the longest pathlength for the highest sensitivity. Test Tubes: Suitable for shorter pathlengths and handling toxic or difficult-to-clean samples. Flow-Through DSPC: Used for highly absorbing samples (e.g., wine, milk) and continuous process monitoring with a pump.
How do I clean CLARiTY’s integrating cavity between measurements?
Filled DSPC: Pipette out the sample, rinse with water/solvent, then rinse with fresh solvent. Test Tubes: Pour out the sample, rinse with water/solvent, clean as needed, and store inverted. Flow-Through DSPC: Flush with water or solvent, clean as needed, and finish with a final rinse
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.