Limits *
Column Isothermal Programmed
PEG 1 280 °C 280 °C
PEG 2 260 °C 270 °C
PEG 3 250 °C 260 °C
PEG 4 250 °C 260 °C
PEG 5 280 °C 300 °C
SLB-IL60 300 °C 300 °C
* Obtained
3. Besman, M., and Coleman, J.E., J. Biol. Chem.,
260(20), 11190-11193 (1985).
4. Latner, A.L. et al., Enzymologia, 40(1), 1-7
(1971).
5. Lazdunski, M. et al., Can. J. Chem., 43(8),
2222-
3. Besman, M., and Coleman, J.E., J. Biol. Chem.,
260(20), 11190-11193 (1985).
4. Latner, A.L. et al., Enzymologia, 40(1), 1-7
(1971).
5. Lazdunski, M. et al., Can. J. Chem., 43(8),
2222-
microcosms by combining whole-cell biosensors
and flow cytometry. Appl. Environ. Microbiol.,
67(1), 239-244 (2001).
6. Cinquina, A. L., et al., Validation of a high-
performance liquid chromatography
acetate (peak 35)
Column Isothermal Programmed
PEG 1 280 °C 280 °C
PEG 2 260 °C 270 °C
PEG 3 250 °C 260 °C
PEG 4 250 °C 260 °C
PEG 5 280 °C 300 °C
SLB-IL60 300 °C 300 °C
Description Cat. No.
SLB-IL60
Ovellet, L., Canadian Journal of Chemistry, 43, 2222-2235 (1965).
5. Besman, M. and Coleman, J.E., Journal of Biological Chemistry, 260, 11190-11193 (1985).
6. Fernley, H.N., The Enzymes (P.D. Boyer ed
3. Besman, M., and Coleman, J.E., J. Biol. Chem.,
260(20), 11190-11193 (1985).
4. Latner, A.L. et al., Enzymologia, 40(1), 1-7
(1971).
5. Lazdunski, M. et al., Can. J. Chem., 43(8),
2222-
.D., in CRC Handbook of Biochemistry
and Molecular Biology, CRC Press (Boca Raton,
FL), p.244 (1990).
5. Pazar, J.H., and Kleppe, K., Biochemistry, 3(4),
578-583 (1964).
6. Nakamura, S., and
transient and stable transfection of eukaryotic cells
Cat. No. 06 366 244 001 0.4 ml
Cat. No. 06 366 236 001 1.0 ml
Cat. No. 06 366 546 001 5 x 1 ml
Store the reagent at
Tris-HCl, 1 mM EDTA, pH
8.0–8.5) and measure the absorbance at 260 nm, 280 nm, and 320 nm using a quartz microcuvette.
The absorbance at 260 nm should be between 0.1 and 1.0 (or within the linear range
Tris-HCl, 1 mM EDTA, pH
8.0–8.5) and measure the absorbance at 260 nm, 280 nm, and 320 nm using a quartz microcuvette.
The absorbance at 260 nm should be between 0.1 and 1.0 (or within the linear range
Tris-HCl, 1 mM EDTA, pH
8.0–8.5) and measure the absorbance at 260 nm, 280 nm, and 320 nm using a quartz microcuvette.
The absorbance at 260 nm should be between 0.1 and 1.0 (or within the linear range
absorbance
at 260 nm and 280 nm using a quartz microcuvette. The
absorbance should be between 0.1 and 1.0 (or within the
linear range of your spectrophotometer). An absorbance
of 1.0 at 260 nm corresponds
absorbance
at 260 nm and 280 nm using a quartz microcuvette. The
absorbance should be between 0.1 and 1.0 (or within the
linear range of your spectrophotometer). An absorbance
of 1.0 at 260 nm corresponds
absorbance
at 260 nm and 280 nm using a quartz microcuvette. The
absorbance should be between 0.1 and 1.0 (or within the
linear range of your spectrophotometer). An absorbance
of 1.0 at 260 nm corresponds