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Apparatus form factors

A serious problem, however, for both paramagnetic and coherent magnetic scattering measurments, at least until higher reflectivity polarizers are available or alternative techniques of polarization analysis are developed, is the low intensity obtained after reflection from the sample as well as from two polarizing crystals. Even for location of apparatus at a high flux reactor, with current techniques the measurement of covalent spin reductions in powder samples can be made as efficiently by profile analysis of a conventional powder diffraction pattern as by polarization analysis. Polarized beam methods including polarization analysis will however, be essential for the determination of form factors. [Pg.37]

The increase of stress during approach to steady-state flow can also be studied it often passes through a maximum. With the device of Pierson and Kovacs, a small correction is made for the compliance of the apparatus. To obtain the normalized stress relaxation function, no form factor b is... [Pg.105]

With a similar principle, the apparatus of Chompff uses Segel-Pochettino geometry if of Fig. 5-1) with a thin foil to contain the viscoelastic liquid between the cylinders. The displacement of the inner cylinder is measured by a differential transformer and the force on the outer cylinder by a ferroelectric ceramic transducer. The frequency range is from 1 to 2500 Hz, and good temperature control is provided over an extremely wide range. The moduli G and G" arp obtained as in equations 19 and 20, with the form factor b specified by equation 13. A related apparatus with continuous recording at constant frequency has been described by Date. ... [Pg.110]

Among the proteins that form part of the transcription machinery are found some cell factors that are produced in limited quantities. They are called cofactors of transcription (NCoA, for nuclear-receptor coactivator NCoI, for nuclear-receptor coinhibitor), formerly known as transcription intermediary factors (TIF) (McDonnell et al. 2002 McKenna et al. 1999). They constitute one of the classes of proteins that form part of the transcription machinery. These proteins are utilized by diverse types of intensifiers, that is to say, by sequences of DNA that anchor transcription factors, of which HRE are a particular case (Gruber et al. 2002 Mester et al. 1995). They do not interact directly with the DNA, but they do with the receptors and with the other elements of the transcription apparatus (Fig. 1.9). [Pg.40]

Fig. 1.40. Model of repression and activation of transcription. The figure illustrates various mechanisms of repression of transcription, a) genes are in a generally repressed states in inactive chromatin. In a first phase of activation the chromatin is restrnctured. b) The promoter is now accessible for the binding of the basal transcription factors and for RNA polymerase II. c) An initiation complex is formed that contains the central components of the transcription apparatns, bnt which enables transcription only at a low rate, d) the binding of repressors to the transcription initiation complex can prevent fnrther activation of transcription at this step, e) the binding of transcription activators to their DNA elements leads to activation of transcription, f) an active repression is affected by proteins that bind seqnence specifically to DNA elements and in their DNA-bound form inhibit the transcritption preventing interactions with the transcription apparatus. Fig. 1.40. Model of repression and activation of transcription. The figure illustrates various mechanisms of repression of transcription, a) genes are in a generally repressed states in inactive chromatin. In a first phase of activation the chromatin is restrnctured. b) The promoter is now accessible for the binding of the basal transcription factors and for RNA polymerase II. c) An initiation complex is formed that contains the central components of the transcription apparatns, bnt which enables transcription only at a low rate, d) the binding of repressors to the transcription initiation complex can prevent fnrther activation of transcription at this step, e) the binding of transcription activators to their DNA elements leads to activation of transcription, f) an active repression is affected by proteins that bind seqnence specifically to DNA elements and in their DNA-bound form inhibit the transcritption preventing interactions with the transcription apparatus.
When mitosis has been completed, the cell requires signals in the form of growth factors to direct towards a new roimd of division. The signals become effective in the first two-thirds of Gi phase. In this time window, the cell is programmed to begin a new cell cycle or to enter Go phase. After a particular point, the restriction point R, no further signals are needed to continue the cell cycle. The cell cycle apparatus is self-contained from this point onwards. S, G2 and M phase occur without external control. The cell cycle may still be halted after crossing the restriction point, however, if the cell detects, via internal control mechanisms or checkpoints, that defects have occurred in the correct course of the phases. [Pg.406]


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See also in sourсe #XX -- [ Pg.98 , Pg.132 , Pg.156 , Pg.602 ]




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Form factor

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