By C. Dennison
It's a truism of technological know-how that the extra primary the topic, the extra universally acceptable it truly is. however, it is very important strike a degree of “fundamentalness” applicable to the duty in hand. For -depth learn of the mechanics of motor autos may inform one instance, an in not anything in regards to the dynamics of site visitors. site visitors exists on a distinct “level” - it's based upon the life of motorized vehicles however the physics and arithmetic of site visitors should be competently addressed by way of contemplating motorized vehicles as cellular “blobs”,with no attention of ways they develop into cellular. to begin a discourse on site visitors with a attention of the mechanics of motorized vehicles could hence be inappropropriate. In scripting this quantity, i've got wrestled with the query of the perfect point at which to handle the physics underlying a few of the innovations utilized in protein isolation. i've got attempted to strike a degree as will be utilized by a mechanic (with possibly a moderate leaning in the direction of an engineer) - i.e. a realistic point, delivering applicable perception yet with minimum arithmetic. a few humans inquisitive about biochemical study have a minimum grounding in chemistry and physics and so i've got attempted to maintain it so simple as attainable.
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Additional resources for A guide to protein isolation
Smith, P. , Krohn, R. , Hemianson, G. , Mallia, A. , Gartner, F. , Provenzano, M. , Fugimoto, E. , Goeke, N. , Olsen, B. J. and Klenk, D. C. (1985) Measurement of protein using bicinchoninic acid. Anal. Biochem. 150, 76-85. 14. Wiechelman, K. , Braun, R. D. and Fitzpatrick, J. D. (1988) Investigation of the bicinchoninic acid protein assay: identification of the groups responsible for color formation. Anal. Biochem. 175, 231-237. 1 5. Bradford, M. M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye-binding.
Farr, A. L. and Randall, R. J. (1951) Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193, 265-275. 1 1 Folin, O. and Ciocalteu, V. (1927) Tyrosine and tryptophan determination in proteins. J. Biol. Chem. 73, 627-650. 12. Peterson, G. L. (1979) Review of the Folin phenol protein quantitation method of Lowry, Rosebrough, Farr and Randall. Anal. Biochem. 100, 201-220. 13. Smith, P. , Krohn, R. , Hemianson, G. , Mallia, A. , Gartner, F. , Provenzano, M. , Fugimoto, E. , Goeke, N.
9). e. from the initial velocity of the enzyme catalysed reaction), in the presence of an excess of substrate (to ensure that a substrate limitation does not restrict the initial velocity). Figure 9. An enzyme dilution curve. 4 A plot of Vo versus [S] yields a so-called substrate dilution curve, such as shown in Fig. 10, which was calculated from the Michaelis-Menten equation, using values of Vmax = 1000 and Km = 90. Figure 10. A substrate dilution curve. Note: The substrate dilution curve must not be confused with the similarly-shaped progress curve.