VIS Spectrophotometer:

Problem seem unsolvable? Try Perkin-Elmer's new ... Problems usually considered too difficult to solve byUV ... Note the shoulder at approximately 700...
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Problem seem unsolvable? Try Perkin-Elmer's new kind of UV/VIS Spectrophotometer: the Model 356. Combine conventional doublebeam performance with highly versatile double-wavelength capa­ bilities and you have the Model 356. Problems usually considered too difficult to solve by UV analy­ sis are done easily and reliably by the Model 356. This different kind of instrument will solve your analytical problems better than any other instrument if you're: a biochemist or biophysicist and your samples are highly turbid; or a plant physiologist and your samples are plant leaves; or a physiologist whose samples are microtomed tissue sections; or a textile or paper chemist who must measure dyes or inks on pa­ per or textiles; or an a n a l y t i c a l chemist w h o must make measurements on over­ lapped absorption bands; or Cytochrome in Yeast

concerned with environmental pollution problems requiring meas­ urement of pesticides, herbicides, polynuclear aromatics and other types of organic and inorganic pol­ lutants; or required to measure the rate of change of two components in a reaction cell simultaneously; or measuring the rates of reac­ tions that produce absorbance changes as small as 0.006A/hr. The Model 356 solves such problems when other spectropho­ tometers can't for a number of reasons. Analyses of turbid samples are done with the large photomultiplier of the Model 356 only 3mm from the sample—light scattering losses are minimized. Band overlap problems are minimized by direct recording of the first derivative curve of the ab­ sorption spectrum. Trace analyses are done by using the 100X scale expansion to achieve lower detection limits.

Simultaneous measurement of concentration changes of two com­ ponents in a single reaction cell can be done by using the DoubleWavelength mode. Kinetics of slow reactions or reactions at high dilution are made using the low noise 100X scale ex­ pansion and the Double-Wave­ length mode. For full details, write for our Model 356 brochure to: Instrument Division, Perkin-Elmer Corporation, 702 Main Avenue, Norwalk, Con­ necticut 06852.

PERKIN-ELMER Bovine Albumin

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WAVELENGTH IN nm CYTOCHROMES IN YEAST - This absorption spectrum of a yeast cell suspension clearly shows the absorption bands of the various cyto­ chromes. To compensate for high turbidity. 8 sheets of filter paper were required in the ref­ erence beam. The sampling geometry and the sensitivity of the Model 356 are such that the transmitted light has been measured through fifteen sheets of Whatmane: No. 2 filter paper at 600 ττ\μ with 1 π\μ bandpass.

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WAVELENGTH IN nm LEAVES — This is the absorption spectrum of a lettuce leaf at liquid nitrogen temperature. Note the shoulder at approximately 700 m/x. This may arise from a component referred to as P700 and is quite difficult to detect in vivo.

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WAVELENGTH IN nm MILK — These curves illustrate the relationship between the absorption spectrum of a milk sam­ ple containing added bovine albumin, and its first derivative curve. The presence of bands hidden in the absorption spectrum is clearly shown in the first derivative curve.

Circle No. 143 on Readers' Service Card

ANALYTICAL CHEMISTRY, VOL. 43, NO. 4, APRIL 1971 ·

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