3. After the incubation period, read the plate at
405 nm on a multiwell plate reader.
4. If the plate cannot be read immediately, add 50 L
of 3 M NaOH solution per 200 L of
Catalogue Number M0545
Sodium Carbonate 5 g
Catalogue Number S2127
Equipment Required but Not Provided
Spectrophotometer or ELISA reader (405 nm)
Cuvettes (3 mL, Catalogue Number C5291
disturbing the cell pellet.
4. Resuspend the cells in 5 mL of EX-CELLTM 405 medium.
5. Count the cells for viability and transfer to a sterile shaker
flask at a seeding density of 2-4 x 105 cells/
L
14420 24420
Liquid Dry Powder
14419 14421
Liquid Liquid
EX-CELLTM 405
500 mL
1000 mL
10 L
1 L
5 L
10 L
50 L
100 L
500 mL
1000 mL
10 L
Applicable Systems
Protein Level
Hydrolysate
minutes at room temperature. The
absorbance can be read at 405 nm on a multiwell
plate reader. The reaction may be stopped by the
addition of 50 µl of 3 N NaOH per 200 µl of reaction
mixture.
minutes at room temperature. The
absorbance can be read at 405 nm on a multiwell
plate reader. The reaction may be stopped by the
addition of 50 µl of 3 N NaOH per 200 µl of reaction
mixture.
extrusion-based bioprinting is 1 to 5 × 106 cells/mL. For example, Human dermal fibroblasts
(HDF) have been printed with TissueFab® - bioink Fibronectin Vis/405 nm at a concentration of 2 × 106 cells
minutes at room temperature. The
absorbance can be read at 405 nm on a multiwell
plate reader. The reaction may be stopped by the
addition of 50 µl of 3 N NaOH per 200 µl of reaction
mixture.
minutes at room
temperature. The absorbance can be read at 405 nm
on a multiwell plate reader. The reaction may be
stopped by the addition of 50 µl of 3 N NaOH per
200 µl of reaction
desired
temperature for 30 minutes.
3. Add 50 L of Stop Reagent to each well.
Tap plate briefly to mix.
4. Read optical density (OD) at 405 nm.
Results
1.
provided (i.e., 1, 2, 3, 4, and 5). For
the 405 nm readings, construct a second dose
response curve using the three calibrators with the
highest concentrations (i.e., 4, 5, and 6).
2. Assign the concentration
reaction mix to standard wells.
3. Measure the absorbance at 405 nm (A405) in
kinetic mode at 37 °C for 60 minutes, taking
readings every 5 minutes.
4. Standard curve may be read in either
mixture of step 2.
4. Add ∼1 µg of Chymase (Cat. No. C8118).
5. Mix by inversion and immediately record the
increase in absorbance at 405 nm for 1 minute
(∆A405/min).
B. 100 µL
spectrophotometrically at 405 nm. The pNPP reaction
may be stopped with the addition of 3 M NaOH
solution and read at 405 nm.
The N9389 tablets are supplied as 50 tablets (50TAB)
or 100 tablets
Transfer 50 L of each Sample Enzyme
dilution to wells of a clear, flat-bottom
96-well plate.
4. In triplicate, prepare Blank Control wells
that contain 50 L of enzyme buffer.
5. Initiate
spectrophotometrically at 405 nm. The pNPP reaction
may be stopped with the addition of 3 M NaOH
solution and read at 405 nm.
The N2765 tablets are supplied as 50 tablets (50TAB)
or 100
ELISA reader and measure the
initial absorbance at 405 nm (t = 0) and then
read at 5 minute intervals for t minutes (where t
can be from 20-60 minutes or even longer for
very dilute samples).
spectrophotometrically at 405 nm. The pNPP reaction
may be stopped with the addition of 3 M NaOH
solution and read at 405 nm.
The N2640 tablets are supplied as 50 tablets (50TAB)
or 100
. Stop solution: 0.2 M NaOH solution
4. Water bath set to 30 °C.
5. Spectrophotometer capable of recording the
absorbance at 405 nm and appropriate cuvettes.
Procedure
The activity of TC-PTP