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Absorbance | Fluorescence | Circular Dichroism | Combination Models | Accessories | New Products |
| As expected, we are delighted with the DW2 upgrade! |  |
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This original spectrophotometer for working on P450, mitochondria, plant and tissue suspensions, and other scattering samples, was developed decades ago by Britton Chance. The performance of this classic has been surpassed by the Olis CLARiTY, but the Aminco DW-2 remains the choice for many laboratories. The DW-2 handles turbidity by positioning a very large faced photomultiplier tube detector millimeters from the sample, thus capturing a good percentage of the light. In addition, as its name implies, it measures two wavelengths simultaneously so as to subtract scatter from the chemistry. The difference spectrum is the answer. If you own this classic, come to us for a comprehensive electro-mechanical modernization; if you need one, confirm that we have one in-stock and purchase a fully modernized and fully warranted system from Olis. |
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 Olis-modernized Aminco DW-2 |
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The technique of dual wavelength spectrophotometry was first developed in 1951 by Dr. Britton Chance who is famous for the pioneering study of ATP synthesis in mitochondria. The Aminco DW-2 and DW-2000 instruments are direct descendents of the original Aminco-Chance dual wavelength spectrophotometer. Investigators working on cytochrome, mitochondria, plant and tissue suspensions, and other particulate samples have trusted the Aminco DW-2 and DW-2000 to produce accurate absorbance readings on their samples for decades. |
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 Olis-modernized Aminco DW-2000 |
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Turbid samples have large backgrounds which make obtaining accurate absorbance readings very difficult. The more turbid the sample, the more incorrect the answer obtained by an ordinary spectrophotometer will be. And, one cannot know that the results are incorrect with the ordinary spectrophotometer without further quantitative measurements. With a scattering sample, the measuring light is deflected (scattered) away from the detector, so close positioning of a detector to the sample is critical. Most absorbance spectrophotometers use small face detectors positioned many centimeters from the sample. The DW-2/2000 uses a large face detector a few millimeters from the sample. However, the "DW-2" gets its name from its more obvious difference from normal spectrophotometers: its use of two monochromators to produce a reference wavelength which is subtracted from the (artificially high) absorbance returned by the sample. The monochromator is motorized, so that it can scan wavelengths. This "Mono 1" is used to scan the spectrum of interest, i.e. 520 580 nm. "Mono 2" is set to the reference wavelength. When the difference between the returned values is taken, one has a "difference spectrum" which is as close to "correct" as one can obtain from a scattering sample. (One is still contending with two effects: the reference beam is not at the same wavelength as the measuring beam, and, without extraordinary measures, one cannot collect all the scattered light and, therefore, cannot get a perfect answer.) When the absorbance value is calculated using the Mono 2 reference, in effect, one produces a "Difference Spectrum". |
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Difference Spectrum = |
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