a Sotax AT
Extend (Sotax, Aesch, Switzerland) with Phosphate buffer pH 6.8 as medium
(wavelength 214 nm, 0.5 mm cuvette).
Results
PERFORMANCE in batch mode comparison
The analysis of the powder properties
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, 15 m x 0.10 mm I.D., 0.08 µm
min.
A gradient elution of 100 % A to 100% B over 10 minutes then 100 % B for 6 minutes.
Samples were monitored at λ = 214 and 254 nm.
RESULTS AND DISCUSSION
More
a coated capillary (50 J.1m x 36 cm).
5. Detection System: Use 214 nm at 0.02-0.05 AUFS or follow manufac-
turer's instructions.
6. Purge Cycles:
To prepare capillary prior to starting run:
a coated capillary (50 J.1m x 36 cm).
5. Detection System: Use 214 nm at 0.02-0.05 AUFS or follow manufac-
turer's instructions.
6. Purge Cycles:
To prepare capillary prior to starting run:
a coated capillary (50 J.1m x 36 cm).
5. Detection System: Use 214 nm at 0.02-0.05 AUFS or follow manufac-
turer's instructions.
6. Purge Cycles:
To prepare capillary prior to starting run:
a coated capillary (50 J.1m x 36 cm).
5. Detection System: Use 214 nm at 0.02-0.05 AUFS or follow manufac-
turer's instructions.
6. Purge Cycles:
To prepare capillary prior to starting run:
a coated capillary (50 J.1m x 36 cm).
5. Detection System: Use 214 nm at 0.02-0.05 AUFS or follow manufac-
turer's instructions.
6. Purge Cycles:
To prepare capillary prior to starting run:
a coated capillary (50 J.1m x 36 cm).
5. Detection System: Use 214 nm at 0.02-0.05 AUFS or follow manufac-
turer's instructions.
6. Purge Cycles:
To prepare capillary prior to starting run:
hour and then the filtrate was collected and analyzed by HPLC –UV. The
results of the analysis at 214 nm are presented in Figure 4 along with HPLC-UV of
warfarin at 5.0 µM . Results obtained by monitoring
hemocyanin
and 300 mug of each conjugated peptide were administered subcutaneously
to female possums (n = 20 per peptide) in complete Freund's adjuvant.
Immunogen doses were repeated 3 and 6 weeks later
Essential
Growth Factor for Normal and Malignant Human
Cells in Tissue Culture. J.Biol. Chem. 214,
845-847.
2. Eagle, H.(1976) Media for Animal Cell Culture.
Tissue Culture Association Manual
negatively
associated with immune infiltration in skin cutaneous melanoma (SKCM). J Immunother. 44(6):214-223.
4. Kaufmann WK, Nevis KR, Qu P, Ibrahim JG, Zhou T, Zhou Y, Simpson DA, Helms-Deaton J
extractables were
detected using a Waters 2489 UV Detector, Model # 87E,
with three detection wavelengths: 214 nm, 254 nm and
280 nm.
Fluorescence Detection. Fluorescent extractables were
detected using a