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Escherichia coli rabbits

Hamaguchi, Y., Yoshitake, S., Ishikawa, E., Endo, Y., and Ohtaki, S. (1979) Improved procedure for the conjugation of rabbit IgG and Fab antibodies with b-D-galactosidase from Escherichia coli using N,N -o-phenylenedimaleimide. J. Biochem. (Tokyo) 85, 1289-1300. [Pg.1070]

Most frequently, extracts of either prokaryotic or eukaryotic origin as such from Escherichia coli, wheat germ or rabbit reticulocytes are employed for cost reasons and availability. While those based on E. coli are unable of post-translational protein modification, eukaryotic extracts do allow synthesis of glycosylated or phosphorylated proteins to some extent when additional components, such as microsomes for glycosylation are added. Care needs to be taken with cell-free systems recombinated from the individual components when a native protein is to be produced that does not fold spontaneously... [Pg.588]

Mack, D. R., and Sherman, P. M. (1991). Mucin isolated from rabbit colon inhibits in vitro binding of Escherichia coli RDEC-1. Infect. Immun. 59, 1015-1023. [Pg.152]

Moon, H. W., Whipp, S. C., Argenzio, R. A., Levine, M. M., and Biannella, R. A. (1983). Attadting and effacing activities of rabbit and human enteropathogenic Escherichia coli in pig and rabbit intestines. Infect. Immun. 41,1340-1351. [Pg.153]

The same liposomal preparation was used to investigate the effect of the administered dose on the biodistribution and pharmacokinetics (41). The effect of the lipid dose of Tc-HYNIC-PEG-liposomes was investigated in the low-dose range (0.02-1.0 pmol/kg), typically for noninvasive imaging applications. The biodistribution and pharmacokinetics of "Tc-HYNIC-PEG-liposomes at various dose levels were studied in rats and rabbits with a focal Escherichia coli infection. Moreover, the pharmacokinetics of Tc-HYNIC-PEG-liposomes at two lipid dose levels were studied in four patients. In rabbits, enhanced clearance was observed at a dose level of 0.02 pmol/kg. The circulatory half-life decreased from 10.4 to 3.5 hours (at 1.0 and 0.02 pmol/kg, respectively). At the lowest dose level, liposomes were mainly taken up by the liver and to a lesser extent by the spleen. Most importantly, the rapid clearance of low-dose PEG liposomes was also observed in humans when relatively low lipid doses were administered as is shown in Figure 4. This study showed that, at very low lipid doses, the biodistribution of PEG liposomes is dramatically altered. [Pg.181]

Gupta, S., J. N. S. Yadava, and J. S. Tandon. Antisecretory (antidiarrheal) activity of Indian medicinal plants against Escherichia coli enterotoxin-in-duced secretion in rabbit and Guinea pig ileal loop models. Int J Pharmacog 1993 31(3) 198-204-... [Pg.432]

Fig. 8. Stability of the rhamnulose 1-phosphate aldolase from Escherichia coli (RhuA) vs. that of the fructose 1,6-bisphosphate aldolase from rabbit muscle (FruA) in phosphate buffer (pH 7.2 25°C ca. 1 Uml ) a) RhuA b) O RhuA, 30% EtOH c) RhuA, 50% DMSO d) FruA... Fig. 8. Stability of the rhamnulose 1-phosphate aldolase from Escherichia coli (RhuA) vs. that of the fructose 1,6-bisphosphate aldolase from rabbit muscle (FruA) in phosphate buffer (pH 7.2 25°C ca. 1 Uml ) a) RhuA b) O RhuA, 30% EtOH c) RhuA, 50% DMSO d) FruA...
Hanes, J.,Jermutus, L., Schaffitzel, C., and Pluckthun, A. (1999). Comparison of Escherichia coli and rabbit reticulocyte ribosome display systems. FEBS Lett, 450(1-2),... [Pg.288]

Bacteria The choice of bacteria for animal models of sepsis depends on the goals of the study. We have used Escherichia coli, because it is one of the most common clinical isolates in humans with sepsis (5). The K-l serotype is associated with invasive infection in humans and rabbits. Bacteria are thawed from a frozen stock and inoculated into 50 mL Lennox-B broth, then grown overnight to stationary phase at 37°C with continuous stirring. After overnight incubation, the... [Pg.320]

Clostridium pasteurianum Azotobacter vinelandii Escherichia coli Neurospora crassa bovine liver rabbit liver cow s milk chicken liver... [Pg.393]

Skrivanova, E. and Marounek, M. 2007. Influence of pH on antimicrobial activity of organic acids against rabbit enteropathogenic strain of Escherichia coli. Folia Microbiol (Praha) 52 70-72. [Pg.148]

Purified 20S proteasome (Methanosarcina thermophila, recombinant, Escherichia coli) was purchased from Calbiochem. Purified eukaryotic 20S proteasome (from rabbit) and eukaryotic 26S proteasome (from rabbit) were purchased from Sigma. Fluorogenic peptide substrates, Suc-Leu-Leu-Val-Tyr-AMC (for the proteasomal chymotrypsin-like activity) and benzyloxycarbonyl, (Z)-Leu-Leu-Glu-AMC (for the proteasomal PGPH activity), were also obtained from Calbiochem, and Z-Gly-Gly-Arg-AMC (for the proteasomal trypsin-like activity) was purchased from Bachem (King of Prussia, PA). [Pg.194]

Scaife, H. R., Cowan, D., Finney, J., Kinghorn-Perry, S. F., and Crook, B. (2006). Wild rabbits (Oryctolagus cuniculus) as potential carriers of verocvtotoxin-producing Escherichia coli. Vet. Rec. 159,175-178. [Pg.114]


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See also in sourсe #XX -- [ Pg.95 ]




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