antibody to Atto 488-NHS (λex 500 nm; λem 522 nm),
Catalog Number 41698, and the conjugate is purified by
gel filtration to remove unbound Atto 488-NHS
fluorophore.
Anti-Nucleolin−Atto 488 recognizes human
pipetting up and down.
13. Add 5 μL of 20X antibody to tubes using the flowing chart.
Tube # Description
1 Treated cells stained with pP38(T180/Y182)-AlexaFluor®488
2 Treated cells stained with
and add 5 µL of either
Anti-phospho-STAT3-Alexa Fluor® 647 or Anti-STAT3-Alexa Fluor® 488 to each sample well.
20. For multiplexing, resuspend the cells in 90 µL of assay buffer and add 5 µL of Anti-phospho
buffer and add 5 µL of either
Anti-phospho-STAT1-Alexa Fluor® 488 or Anti-STAT1-PerCP to each sample well.
17. For multiplexing, resuspend the cells in 90 µL of assay buffer and add 5 µL of Anti-phospho
pipetting up and down.
16. Add 5 μL of 20X antibody to tubes using the flowing chart.
Tube # Description
1 Treated cells stained with Bcl-2 AlexaFluor®488
2 Treated cells stained with
buffer and add 5 µL of either
Anti-phospho-Src-Alexa Fluor 488 or Anti-Src-Alexa Fluor 647 to each sample well.
22. For multiplexing, resuspend the cells in 90 µL of assay buffer and add 5 µL of Anti-phospho
buffer and add 5 µL of either
Anti-phospho-PLC-γ1-Alexa Fluor 488 or Anti-PLC-γ1-PE to each sample well.
22. For multiplexing, resuspend the cells in 90 µL of assay buffer and add 5 µL of Anti-phospho
responsible for formazan patterns in
dehydrogenase histochemistry. Experientia, 17,
136 (1961).
10. J. Histochem. Cytochem., 5, 515 (1957).
11. Bernofsky, C., and Swan, M., An improved cycling
assay
Dye (Water) is a far red nuclear stain
for live cells. The dye can be excited by wavelengths from 488 to 647nm
and emits far red fluorescence with emission maximum at 694nm. The
dye specifically stains
in
inhibition by beta-mercaptoethanol,
phosphoramidate, and fluoride. Can. J. Biochem.,
58, 481-488 (1980).
6. Dixon, N.E. et al., Metal ions in enzymes using
ammonia or amides. Science, 191, 1144
in
inhibition by beta-mercaptoethanol,
phosphoramidate, and fluoride. Can. J. Biochem.,
58, 481-488 (1980).
6. Dixon, N.E. et al., Metal ions in enzymes using
ammonia or amides. Science, 191, 1144
in
inhibition by beta-mercaptoethanol,
phosphoramidate, and fluoride. Can. J. Biochem.,
58, 481-488 (1980).
6. Dixon, N.E. et al., Metal ions in enzymes using
ammonia or amides. Science, 191, 1144
in
inhibition by beta-mercaptoethanol,
phosphoramidate, and fluoride. Can. J. Biochem.,
58, 481-488 (1980).
6. Dixon, N.E. et al., Metal ions in enzymes using
ammonia or amides. Science, 191, 1144
2. Place white blood cells in clean 17 x 100 mm tube.
3. Resuspend cells in 5 ml citrate buffer solution.
4. Centrifuge for 5 minutes (300 x g) at room temperature.
5. Aspirate supernatant and resuspend
and down.
16. Add 5 μL(Guava) or 10 μL(Other) of 20X antibody to tubes using the flowing chart.
Tube # Description
1 Untreated cells stained with pSMC1-AlexaFluor®488
2 Treated cells stained