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The two key properties in single-phase ow are the uid density and the viscosity. The density is quite straightforward; it is the mass per unit volume. In turbulent ow, pressure drop is directly proportional to density, so that the accuracy of the density is the accuracy of the pressure drop prediction. It is easy to get better than 1% accuracy on such values. Viscosity, on the other hand, is a more complex measurement. Low viscosity systems usually run in turbulent ow, where the viscosity has little or no effect on mixing or pressure drop. For low viscosity material the prime use of the viscosity is in calculating a Reynolds number to determine if the ow is laminar or turbulent. If turbulent, little accuracy is needed. An error in viscosity of a factor of 2 will have negligible effect. In laminar ow, however, the viscosity becomes all important and pressure drop is directly proportional to it, so that an accuracy of 10% or less is often required. For laminar processing a complete relation of stress versus strain or shear rate versus shear stress is required. See 4 for the means and type of data required.

loads/macosx/automator/.

The enclosing square brackets around FileMaker s default privilege set names enable you to easily differentiate them from other privilege sets in your solution files. When creating your own privilege sets, you can choose to enclose their names in square brackets. However, I recommend against doing so, to preserve and underscore the distinction between default privilege sets and those created specifically for the solution.

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face as indicated. Push/Pull the surface to a 1 thickness. Make it a component called Bench Rail. Add color. Rotate the component to vertical.

box in the Rules preferences. Third, be aware that the autoresponder will include the full message text plus any attachments. If you want to avoid returning the full text and attachments, you need to use an AppleScript such as the one you can download from About.com (http://email.about.com/od/macosxmailtips/qt/et022106.htm).

Digital Palomar Observatory Sky Survey; Sloan Digital Sky Survey;

Speakers (AirPort Express only). Connect your speakers or home stereo to the AirPort Express s stereo mini-jack via either an analog audio cable or a digital audio cable. Power. If you have an AirPort Express, plug it directly into a socket. For other AirPort models, connect the power supply to a socket, and plug the connector into the AirPort. With the AirPort connected, configure it as follows from your iMac:

16. IEEE, IEEE Standard VHDL Language Reference Manual (IEEE Srd 1076-2001), Institute of Electrical and Electronics Engineers, 2001.

42 OVERVIEW OF METHODS Many of the methods in current use are based on those developed for mouse embryonic stem cells (mESCs), namely, the formation of aggregates in suspension called embryoid bodies (EBs) Many mESCs will start to beat spontaneously between 4 and 10 days of initial aggregation depending on the number of cells in the aggregate or the cell line It is believed that the formation of an outer layer of (extra)embryonic endoderm on the EBs may be important as a source of differentiation signals since it is known that in normal development of multiple species endoderm is essential for and signals to the anterior mesoderm during heart formation The conversion of undifferentiated stem cells to cardiomyocytes is generally a low-ef ciency process Much of the literature on improving these ef ciencies concerns activating speci c developmentally relevant signaling pathways while the cells are growing as EBs.

The wnt and bone morphogenetic protein (BMP) signaling pathways have proved most potent in this context The rst report of cardiomyocytes derived from hESC [Kehat et al, 2001] appeared almost three years after hESC were rst derived from blastocyst stage embryos [Thomson et al, 1998] To induce cardiomyocyte differentiation, hESCs (cell line H92) were dispersed using collagenase IV into small clumps (3 20 cells) and grown for 7 10 days in suspension to form EB-like structures, comparable to mESCs but apparently without the distinct outer layer of endoderm cells After these EBs were plated onto gelatin-coated culture dishes, beating areas were rst observed in the outgrowths 4 days after plating (11 14 days after the start of the differentiation protocol) A maximum in the number of beating areas was observed 20 days after plating (27 30 days of differentiation), with 8.