Reproducibility potential development stage

The investigation of electron ionization is clearly in the early stages in comparison with the electron transfer studies, and additional work on the influence of orientation on Augmentation will be required before a coherent pattern emerges and a model for fragmentation can be attempted. However, a simple model that considers ionization in terms of the Coulomb potential developed between the electron and the polar molecule, taking the electron transition probability into account, reproduces the main experimental features. This model accounts qualitatively for the steric effect measured and leads to simple, generally applicable, expressions for the maximum (70 eV) ionization cross section. 

We present here the results of abundance measurements of iron, calcium and nickel in four open clusters, from UVES spectra of solar type stars. A code developed by one of the authors (Francois) performs line recognization, equivalent width measurements and finally obtains the abundances by means of OSMARCS LTE model atmosphere [4]. Temperature, gravity and microturbulence velocity have to be input to the program. This is made in an automatic way for a grid of values chosen on photometric basis. Those that best reproduce excitation and ionization equilibria are selected and used, namely when no significant trend of the computed abundances is seen, neither versus the excitation potential of the line nor versus its equivalent width, and for which the abundances obtained with lines of different ionization stages of the same specie give equal results within the errors. This check is made with iron lines, we have in fact at least thirty Fe I lines in each star, and six Fell lines. 

The MS techniques described previously for characterization of the final recombinant protein product can be applied at all stages during process development. MS might be used upstream to define clone selection, processing format, and purification steps, and downstream to characterize the final product, ascertain lotto-lot reproducibility, determine stability, and define the formulation of biopharmaceutical molecules. Presented here are some examples found either in the literature or from our own experience in which MS has been found to be a useful or necessary tool. Potential limitations of MS methods are discussed, and when appropriate, other analytical methods are mentioned that can be alternatives to MS and are also efficient tools for biopharmaceutical development. 

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