mized, when after a sterilization time of 6 minutes at 121° ± 0.5 °C
all ampoules contain living spores, whereas after 15 minutes auto -
claving at 121° ± 0.5 °C all spores are dead. For the period inbetween
optimized, when after a sterilization time of 6 minutes at 121 ±
0.5 °C all ampoules contain living spores, whereas after
15 minutes autoclaving at 121 ± 0.5 °C all spores are dead. For
the period in between
).
5. Lindner R. and Ungewickell E., J. Biol. Chem.,
267: 16567-73 (1992).
6. Robinson M. S. and Kries T. E., Cell, 69:
129-38 (1992).
7. Klumpermann J., et al., J. Cell Biol.
3 µm are a standard
equipment of the instrument. The membrane filter is autoclavable up
to 5 times at 121 °C. It is the user's responsibility to ensure effective
autoclaving.
Note:
Cleaning ·
Biol., 11, 122-129
(2001).
5. Helenius, A., and Aebi, M., Ann. Rev. Biochem., 73,
1019-1049 (2004).
6. Bedard, K., et al., Int. Rev. Cytol., 245, 91-121
(2005).
7. John
molecular mass of approximately 14 kDa
under reducing conditions. Human and mouse neurturin
share 91% amino acid sequence identity. Neuturin also
shares 42% similarity with glial cell-derived neuro-
supplied with a 0.2 µm
membrane filter (red color code). The membrane filter is autoclavable up
to 5 times at 121 °C (250 °F). The filter with 0.2 µm pore size (for cell
culture) is sufficient to meet class
1B-adrenergic
receptor in transgenic mice induces cardiac hypertrophy. Proc. Natl. Acad. Sci. USA 91:
10109-10113.
For research use only; not for use as a diagnostic.
Unless otherwise
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