Download Analytic Sets (London school 1978) by C. A. Rogers, J. E. Jayne et. al. (editors) PDF

By C. A. Rogers, J. E. Jayne et. al. (editors)

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Over ice. 3. 1 M phosphate buffer pH 8, and re uspend in 6 ml of the same buffer. 4. Add a cold aqueous solution of protein (5-15 mg in 2-3 ml) under stirring. 5. Ke p overnight under stirring at 4 0c. 6. 1 M in NaHC0 3 and water. 7. Resuspend in water (5 ml) and store at 4°C. 3 Remarks concerning the choice of coupling techniques The characteristic of the respective biocomponent determines the choice of the coupling technique. Enzymes unstable at pH values> 8 must be immobilized with th h lp oft chnique rno t effective at low pH valu s ( .

Oil in water detection and monitoring..... ............... Oil sample fingerprinting.................................................................. Bacterial viability............ ................ ........ Chlorophyll measurement and algae monitoring.................................. DNA/RNA quantification................................................................... Fluorescent tracer studies................................................................. Protein quantification, histamine analysis, vitamin assays, aflatoxin analysis, antibiotic sensitivity testing, enzyme activity and cell proliferation.................................................................................

Wash with toluene and acetone and react immediately with thioacetic acid (10% solution buffered to pH 6) for 30 min. t. 30 Fritz Pittner 3. Couple with carbodiimide as listed above. 4. Immerse the activated carrier in a solution of amino-groups containing biocomponent (e. g. 1 M phosphate buffer pI 7) for 2 h. 5. Rinse several times with 4 M saline to eliminate adsorbed protein and store wet at a °_5 0c. 4 Immobilization of biocomponents onto nylon Nylon is readily available in a wide variety of physical forms, such as fIlm , membranes, powders, hollow fibers, and tubes.

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