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Substituting C(t) in the Schrodinger equation produces HC aEg e i(Eg t=h ) jCg l aH1 e i(Eg t=h ) jCg l bEe e i(Ee t=h ) jCe l bH1 e i(Ee t=h ) jCe l ih @C @t

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or, more compactly,

0.8500 1.0000 0.8500 0.7225





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oligonucleotides and lipids. Other highly selective bioconjugations to probes are made possible in oligo- or polypeptides in other ways. For instance, N-terminal serine or threonine residues of an oligo- or polypeptide can be selectively oxidised by oxidative cleavage to give aldehydes (Figure 4.20), which are primed for bioconjugation to uorescent probes with amines or hydrazines. Furthermore, tyrosine residues can sometimes be selectively modi ed by ortho-nitration using tetranitromethane followed by reduction to form an aminotyrosine (Figure 4.21). Alternatively, a particularly innovative approach is to use a puri ed enzyme (transglutaminase) to speci cally modify glutamine residues with amine-containing probes in the primary amide functional group (Figure 4.22). The presence of an aliphatic spacer between the amine functional group and the uorescent probe increases reaction ef cacy, especially when a cadaverine spacer is used (as shown). One extreme view of chemical introduction of an extrinsic uorescent probe is found in the case of the alanine derivative of the uorophore 6-dimethylamino-2-acylnaphthalene (DAN) (Figure 4.23). This derivative uorophore, given the trivial name Aladan, is incorporated into a polypeptide by solid-phase synthetic chemistry (although a molecular biology technique known as nonsense suppression is now available for the introduction of unnatural aminoacid residues into recombinant proteins). The uorescent emission maximum (Imax ) of Aladan shifts dramatically on different solvent exposures, from 409 nm in heptane to 542 nm in water, yet at the same time remains only mildly changed by variations in pH or salt concentration. This compares to a maximum environment-mediated shift of around 40 nm for intrinsic tryptophan uorescence. In addition, there is little spectral overlap between extrinsic Aladan uorescence and intrinsic uorescence from tryptophan or tyrosine.

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Adaptive Wireless Tranceivers L. Hanzo, C.H. Wong, M.S. Yee Copyright 2002 John Wiley & Sons Ltd ISBNs: 0-470-84689-5 (Hardback); 0-470-84776-X (Electronic)

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Entering Formulas into Your Worksheets ..................................................................................181 Entering formulas manually ............................................................................................183 Entering formulas by pointing ........................................................................................183 Pasting range names into formulas ..................................................................................183 Inserting functions into formulas ....................................................................................184 Function entry tips ........................................................................................................186 Editing Formulas ......................................................................................................................187 Using Cell References in Formulas ............................................................................................187 Using relative, absolute, and mixed references ................................................................187 Changing the types of your references ............................................................................190 Referencing cells outside the worksheet ..........................................................................190 Referencing cells in other worksheets ..................................................................190 Referencing cells in other workbooks ..................................................................190 Using Formulas In Tables ..........................................................................................................191 Summarizing data in a table ............................................................................................191 Using formulas within a table..........................................................................................193 Referencing data in a table ..............................................................................................194 Correcting Common Formula Errors ........................................................................................195 Handling circular references............................................................................................196 Specifying when formulas are calculated ........................................................................198 Using Advanced Naming Techniques ........................................................................................199 Using names for constants ..............................................................................................199 Using names for formulas ..............................................................................................199 Using range intersections ................................................................................................200 Applying names to existing references ............................................................................202 Tips for Working with Formulas................................................................................................203 Don t hard-code values....................................................................................................203 Using the Formula bar as a calculator ............................................................................203 Making an exact copy of a formula..................................................................................204 Converting formulas to values ........................................................................................204

Af = E,(QF,')

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-30 -35 -40

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