ADAR1.
The antibody may be used in various immunochemical
techniques including immunoblotting (~110 kDa) and
immunoprecipitation. Detection of the ADAR1 band by
immunoblotting is specifically inhibited
striatin, 110 kDa,
by immunoblotting. Staining of the striatin band is
specifically inhibited with the immunizing peptide.
Striatin is a neuronal, membrane associated protein,
780 amino acids, 110 kDa
kDa,10 and it is composed of α-
, β-, β'-, γ-, δ-, ε-, and ζ-COP.3,9 Best characterized is
the 110 kDa β-COP component, which has homology in
primary structure to the β-adaptin component of
clathrin-coated
with a C-
terminally added lysine.
Anti-FGFR-1 may be used for immunoblotting (approx-
imately 110 kDa and 120 kDa), immunoprecipitation, and
immunohistochemistry. Staining of the product is specif
MAP Mouse Cytokine/Chemokine Panel Catalog # MPXMCYTO-70K
Control Catalog # MXM6070-2 LOT# MCY-110 and MCY-210
Note: The Quality Control Ranges are generated with overnight assay format using serum
Conditions for Hole Transport Ink
The film should be annealed at preferred temperatures
of 110–175 °C on a hot plate for 15–30 minutes in air or
an inert atmosphere.
Note: Temperature should not exceed 180
Conditions for Hole Transport Ink
The film should be annealed at preferred temperatures
of 110–175 °C on a hot plate for 15–30 minutes in air or
an inert atmosphere.
Note: Temperature should not exceed 180
active constituents of compound
48-80. J. Med. Chem., 15(3), 320-323 (1972).
5. Papacostas, et al., Arch. Int. Pharmacodyn. Ther.,
120, 353 (1959).
6. Bronner, C., et al., Compound 48/80 is a potent
rabbit serum proteins.
Anti-Protein Kinase D (PKD/PKCµ) recognizes human
and mouse PKD/PKCµ (110 kDa). Applications include
the detection of PKD/PKCµ by immunoblotting and
immunoprecipitation. Staining
water indicated on the product label. This
results in a solution containing 20 mM HEPES, pH 7.5,
110 mM potassium acetate, 5 mM magnesium acetate,
0.5 mM EGTA, and 5% sucrose. The concentration of
the
30 °C for 15 minutes.
5. After the 15 minute incubation, stop the reaction by
adding 25 µl of the ADP-Glo reagent. Shake the
plate and incubate for 40 minutes at ambient
temperature.
6. Add 50 µl
30 °C for 15 minutes.
5. After the 15 minute incubation, stop the reaction by
adding 25 µl of the ADP-Glo reagent. Shake the
plate and incubate for 40 minutes at ambient
temperature.
6. Add 50 µl
30 °C for 15 minutes.
5. After the 15 minute incubation, stop the reaction by
adding 25 µl of the ADP-Glo reagent. Shake the
plate and incubate for 40 minutes at ambient
temperature.
6. Add 50 µl
30 °C for 15 minutes.
5. After the 15 minute incubation, stop the reaction by
adding 25 µl of the ADP-Glo reagent. Shake the
plate and incubate for 40 minutes at ambient
temperature.
6. Add 50 µl
inhibition
of the current evoked by stepping from the holding potential of -30 mV to -110
mV was 66 ± 6% (n =6). This is in contrast to the effect of the same
concentration of genistein on HCN 1 currents
Solution
Product Number C 3672
Lot Number 21K8803
CAS Number [70420-71-2]
Concentration 110 µg Codeine-d3 Hydrochloride
(equivalent to 98.6 µg free base)/mL
GC grade methanol (conc. corrected
well using a horizontal shaker or
by pipetting. Incubate the plate at plate for
10–15 minutes at 25 C or for 80–110 minutes at
4 C. Protect the plate from light during the
incubation.
3. Measure
sonication.
14
Various publications report preparation in DMSO at
50 mg/mL
13
and at 110 mg/mL.
15
A 10 mM aqueous solution can be prepared by
warming in a boiling water bath.
together with
substoichiometric amounts of several other proteins.20,22
Best characterized is the 110 kDa β-COP component
which has homology in primary structure to the
β−adaptin component of clathrin-coated
60K-PX29, HCYTMAG60PMX29BK, HCYTOMAG-60K-PX30, HCYTMAG60PMX30BK
Control Catalog # MXH6060-2 Lot # HCY-110 and HCY-210
***Additional Analytes on reverse side***
Note: The Quality Control Ranges are