Chromolith® HR RP-18e 50×2 mm I.D. column at 228 nm.
Figure 4. Calibration curves of six cannabinoid analytes obtained with a Chromolith® HR RP-18e 50×2 mm I.D. column at 228 nm. Calibration
curve ranges
Expiration Date May 2005
Storage
2-8°C; Aft
O
C H3
C H3
OH
Mattson Galaxy 3020 FT-IR
70 eV Electron Ionization Mass Spectrum
40 60 80 100 120 140 160 180 200 220 240 260
Storage 2-8°C; After opening, transfer contents to
small vial provided for your convenience.
Mattson Galaxy 3020 FT-IR
70 eV Electron Ionization Mass Spectrum
40 60 80 100 120 140 160 180 200 220
Storage 2-8°C; After opening, transfer contents to
small vial provided for your convenience.
Mattson Galaxy 3020 FT-IR
70 eV Electron Ionization Mass Spectrum
40 60 80 100 120 140 160 180 200 220
densitometry)
Figure 2.
Specific Activity of Typical Lot
228–308 nmole/min/mg
Procedure
Preparation Instructions
Kinase Assay Buffer – 25 mM MOPS, pH 7.2, 12.5 mM
glycerol 2-phosphate, 25 mM MgCl2
1946)
Immunogen: Recombinant protein Ephrin-A5
Immunogen Sequence: GI # 4503487, sequence 188 - 228
The product is a clear, colorless solution in phosphate
buffered saline, pH 7.2, containing 0.02%
)
Immunogen: Recombinant protein Homeobox C11
Immunogen Sequence: GI # 7657166, sequence 1 - 228
The product is a clear, colorless solution in phosphate
buffered saline, pH 7.2, containing 0.02%
developed in rabbit using a synthetic
peptide, RPQKRLSSSRRAG corresponding to human
gata5 (amino acids 228-240) conjugated to BSA as
immunogen. The antibody is affinity-purified using the
immunizing peptide
A purified peptide corresponding to amino acid residues 213-228 of human Caγ2
(Accession O88602).
APPLICATIONS: Western blot: 1:200 using ECL on rat brain membranes.
Dilutions should be made
Buffer.
Working Mixture (8 ml) – To 8 ml of 1 Assay Buffer,
add 228 l of the diluted Enzyme Solution (6 units/ml)
and 228 l of DTNB Stock Solution (1.5 mg/ml). Mix
immunoprecipitation
experiments. Does not cross-react with µ-calpain,
n-calpain, calmodulin (Cat. No. C-228) or calpastatin.
Epitope mapping studies indicate the epitope is
between amino acids 502-699 (domain
-gamma: a
new member of p38 group of MAP kinases.
Biochem. Biophys. Res. Commun., 228, 334-340
(1996).
2. Ho, R.C. et al., p38gamma MAPK regulation of
glucose transporter expression and glucose