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Additional info for Methods of Biochemical Analysis, Volume 21
55 56 G. Titration.. . . . 56 H. Gravimetric.. . . . . . .. . . 57 .. . .. . . .. 58 Nondestructive Analysis. . . . . . . . . . 58 1. Neutron Activation Analysis. . . . . . . . . . . 58 A. Methods of Measurement. . . . . . . . . . . . . . . . _ . _ . . . . 59 B. Modes of Activation.. . . . . . . . . . .......................... 61 . .. . 63 V. Methods.. . . , . . . . .......... 1. Method A 3. Method C . . . . . .
_ . _ _ . .. . . . . . 66 67 67 70 72 74 39 40 0. E. OLSON, I . S. PALMER, A N D E. I . WHITEHEAD I. INTRODUCTION Selenium occurs naturally in biological materials at levels that vary from a few parts per billion to a few per cent. Methods for its determination in these materials must, therefore, cover a very wide range of concentrations. As a result there have been developed a number of procedures for selenium analysis, many of which are discussed briefly in a review by Watkinson (1).
5. Treatment of UDP Glucuronyltransferase and Glucose-6-Phosphatase with Phospholipases REAGENTS. 1 . Partially purified phospholipase A , 10 mg/ml, from Naja nuja or Crotalus adamanteus venom. Phospholipase C from Clostridium welchii, 10 mg/ml, prepared fresh each day. 2. 1M. 3. 0. 4. 25M sucrose. 5. 25M. Procedure. 025 ml CaC12 is added if phospholipase A fromCrotalusadumanteus or phospholipase C is to be used. 1 ml phospholipase C. 005M to inhibit further action of phospholipase. There is no correlation between the rate of hydrolysis of microsomal phospholipids and phospholipase-induced modifications in the properties of glucose-6-phosphatase (4), and the time course for these effects are variable for different enzymes and in different species.
Methods of Biochemical Analysis, Volume 21