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Extracts copyright basics

Figure 7.2 The basic Soxhlet extraction system. From Dean, J. R., Extraction Methods for Environmental Analysis, Copyright 1998. John Wiley Sons Limited. Reproduced with permission. Figure 7.2 The basic Soxhlet extraction system. From Dean, J. R., Extraction Methods for Environmental Analysis, Copyright 1998. John Wiley Sons Limited. Reproduced with permission.
Figure 7. Basic steps involved in the standard batch hot-water flotation (batch extraction) test. (Reproduced from reference 52. Copyright 1989 Alberta Oil Sands Technology and Research Authority.)... Figure 7. Basic steps involved in the standard batch hot-water flotation (batch extraction) test. (Reproduced from reference 52. Copyright 1989 Alberta Oil Sands Technology and Research Authority.)...
Fig. 2 Two-dimensional PAGE analysis of sperm-associated proteins on condensed chromatin and following chromatin decondensation in egg extract and purified nucleoplasmin. Sperm nuclei were incubated in either (A) buffer, (B) Xenopus egg HSS, or (C) purified egg nucleoplasmin for 10 min. The nuclei were then pelleted, washed, and the chromatin-associated proteins were extracted with acid and analyzed in the first dimension by Triton-acid-urea (TAU)-PACE (left to right) and in the second dimension by SDS-PAGE (top to bottom). The positions of the core histones are indicated as H2A, H2B. H3. and H4 and the sperm-specific basic proteins as X and Y. The arrowheads and arrow indicate the positions of the cleavage-stage linker histone. B4, and Xenopus HMG-2, respectively (Dimitrov et at., 1994). [Reproduced from Philpott and Leno (1992) Copyright Cell Press.]... Fig. 2 Two-dimensional PAGE analysis of sperm-associated proteins on condensed chromatin and following chromatin decondensation in egg extract and purified nucleoplasmin. Sperm nuclei were incubated in either (A) buffer, (B) Xenopus egg HSS, or (C) purified egg nucleoplasmin for 10 min. The nuclei were then pelleted, washed, and the chromatin-associated proteins were extracted with acid and analyzed in the first dimension by Triton-acid-urea (TAU)-PACE (left to right) and in the second dimension by SDS-PAGE (top to bottom). The positions of the core histones are indicated as H2A, H2B. H3. and H4 and the sperm-specific basic proteins as X and Y. The arrowheads and arrow indicate the positions of the cleavage-stage linker histone. B4, and Xenopus HMG-2, respectively (Dimitrov et at., 1994). [Reproduced from Philpott and Leno (1992) Copyright Cell Press.]...
FIGURE 13.1 Schematic pictures of different membrane extraction phase systems, (a) One-phase membrane extraction (dialysis), (b) three-phase polymeric membrane extraction, (c) three-phase SLM extraction, and (d) two-phase SLM extraction system (MMLLE). (From Comprehensive Sampling and Sample Preparation, Jonsson, J.A. (J. Pawliszyn and H. Lord, eds.), Membrane extraction General overview and basic techniques, pp. 461-474, Copyright 2012, with permission from Elsevier.)... [Pg.379]


See other pages where Extracts copyright basics is mentioned: [Pg.161]    [Pg.51]    [Pg.379]    [Pg.390]   
See also in sourсe #XX -- [ Pg.80 , Pg.83 , Pg.84 , Pg.85 ]




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