mg/l PO4-P (307 mg/l PO43-) must
be diluted with distilled water.
• The pH must be within the range 0 - 10.
Adjust, if necessary, with sulfuric acid.
• Filter turbid samples.
7. Procedure
constant6 of 5 x 104 M-1. The
association is accompanied by an enhancement of
approximately 35% in α-helical content.7
Unlike Apo A-I, Apo A-II possesses no activating
properties for lecithin-cholesterol
constant of 5 x 104M-1.6 The association is
accompanied by an enhancement of approximately
35% in a α-helical content.7
Unlike Apo A-I, Apo A-II possesses no activating
properties for lectin-cholesterol
Chemioterapia, 4(6), 424-428 (1985).
4. Wright, A. J., The penicillins. Mayo Clin. Proc.,
74(3), 290-307 (1999) and 74(11), 1184 (1999).
5. McFarland, M. M., et al., Time-survival studies for
quantifying
cultures
suspected to contain Pseudomonas so that individual colonies
develop.
Incubation: up to 7 days at 35 °C.
Check for bacterial growth after 24, 48 and 72 hours and then
after 6 days.
Pseudomonas aeruginosa
Filtrar las muestras turbias.
7. Técnica
Agua destilada 1) 8,0 ml Pipetear en un tubo de ensayo.
(10 - 35 °C)
Muestra preparada 0,50 ml Añadir con pipeta y mezclar.
(10 - 35 °C)
Reactivo PO4-1 0,50 ml
cultures
suspected to contain Pseudomonas so that individual colonies
develop.
Incubation: up to 7 days at 35 °C.
Check for bacterial growth after 24, 48 and 72 hours and then
after 6 days.
Pseudomonas aeruginosa
41(3), e49 (2013).
18. Liu, C. et al., Am. J. Physiol. Gastrointest. Liver
Physiol., 307(7), G749-G759 (2014).
19. Tu, K. et al., Hepatology, 61(1), 361-374 (2015).
20. Perrody, E.
Biochem. J. 296 843-849 (1993).
6. Stokoe, D., et al., FEBS Lett. 313 307-313 (1992).
7. Zhou, M., et al., J. Biol. Chem. 268 35-43 (1993).
8. Engel, K., et al., FEBS Lett. 336 143-147 (1993).
9. Zu
ULR
(Method number 307)
5
1.0 – 40.0 ± 1.0 50 mm Yes 100/300/600 Bromate ULR
(Method number 307)
6
2.5 – 100.0 ± 2.5 100 mm No 600 Bromate LR
(Method number