331 |
Targeting ubiquitin chains with deubiquitinasesYe, Yu January 2012 (has links)
No description available.
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332 |
The isolation and characterization of succinic dehydrogenase from chromatophores of Rhodospirillum rubrumQuirk, Jane Maryann, 1944- January 1968 (has links)
No description available.
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333 |
Kinetic and mass transfer characteristics of pancreatic ribonuclease immobilized on porous titaniaDale, Bruce Edwin, 1950- January 1976 (has links)
No description available.
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334 |
The crystallization and x-ray characterization of the phospholipase Ab2sgbs of Crotalus AdamanteusPlacilla, William John, 1952- January 1976 (has links)
No description available.
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335 |
Studies in biological surface science: microfluidics, photopatterning and artificial bilayersHolden, Matthew Alexander 30 September 2004 (has links)
Herein is presented the collective experimental record of research performed in the Laboratory for Biological Surface Science. These investigations are generally classified under the category of bioanalytical surface science and include the following projects. Chapters III and IV describe the creation of a microfluidic device capable of generating fixed arrays of concentration gradients. Experimental results were matched with computational fluid dynamics simulations to predict analyte distributions in these systems. Chapters V and VI demonstrate the discovery and utility of photobleaching fluorophores for micropatterning applications. Bleached fluorophores were found to rapidly attach to electron rich surfaces and this property was used to pattern enzymes inside microfluidic channels in situ. Finally, Chapter VII exhibits a method by which solid supported lipid bilayers can be dried and preserved by specifically bound proteins. The intrinsic property of lateral lipid mobility was maintained during this process and a mechanism by which the protein protects the bilayer was suggested.
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Studies of reactions catalysed by purified pea cellulasesWong, Yuk-Shan January 1976 (has links)
No description available.
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337 |
Enzymatic studies on GM1 ganglioside biosynthesisRabinowitz-Kaplan, Fëıge. January 1981 (has links)
An enzyme that catalyzed the terminal step in GM(,1) ganglioside biosynthesis was demonstrated in rat brain and rat liver microsomal preparations. This galactosyltransferase enzyme could be solubilized from the Golgi fraction of rat liver homogenates. Anion exchange chromatography resolved two distinct enzymes with activity toward GM(,2) ganglioside. These two activities could be distinguished by such properties as pH optima, detergent requirements, and isoelectric points. The two enzymes had similar molecular weights and cation requirements. / Extensive characterization of the acceptor specificities of galactosyltransferase enzymes present in solubilized Golgi preparations led to the identification of five enzyme reactions. Two activities were identified which had a requirement for acceptors within the glycoprotein family. A single activity supported the biosynthesis of GM(,1) ganglioside only. The fourth galactosyltransferase activity catalyzed the incorporation of galactose into both ganglioside and glycoprotein.
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338 |
An investigation of cyclic AMP receptor protein (CRP)-Induced DNA bending at the lac, gal and malT operonsKelly, Patrick John 08 1900 (has links)
No description available.
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339 |
Sequencing and characterization of a carrot cDNA clone encoding a protein kinase fragmentLindzen, Eric C. 12 1900 (has links)
No description available.
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340 |
A probe of the rotenone-piericidin a-amytal binding site of NADH-coenzyme Q reductbase by structure-activity relationships between the new natural benzofuran inhibitor hydroxytremetone and related benWilson, Lois Kathryn 05 1900 (has links)
No description available.
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