SCM133
PluriSTEM® Dispase-II Solution
Dispase-II has proven to be a rapid and effective, yet gentle, agent for separating many tissues and cells grown in vitro.
Synonym(s):
Dispase, Dispase 2
About This Item
Recommended Products
Quality Level
form
liquid
manufacturer/tradename
PluriSTEM®
concentration
1 mg/mL in sterile DMEM/F-12
technique(s)
cell culture | mammalian: suitable
cell culture | stem cell: suitable
shipped in
dry ice
General description
PluriSTEM Dispase-II has been validated to work alongside PluriSTEM Human ES/iPS Medium (SCM130) for the culture and passage of human embryonic and induced pluripotent stem cells.
Dispase-II enzyme is produced in Bacillus polymyxa.
Application
1. Coat 6-well plates with 1:20 Matrigel coating (1.5 ml per well). Incubate at 2-8ºC overnight or coat at RT for at least 30 minutes to 1 hour before use.
2. Remove matrigel coating. Add 2 mL of Complete Media per well.
3. Remove areas of differentiation within culture.
4. Aspirate media.
5. Wash once with 2 mL PBS.
6. Add 1.5 mL Dispase II per well. Incubate for 37ºC for 7 minutes.
7. Wash 2X with 2 mL PBS, w/o Mg and Ca.
8. Add 2 mL Complete Media to each well and use cell scraper to detach colonies.
9. Collect scrapped cells in 15 ml conical tube.
10. Spin 800 rpm for 5 minutes
11. Resuspend in appropriate volume of complete media. Typical splitting ratio is 1:5 – 1:6 depending upon cell density. Cells should be ready for passaging in 5-6 days time using PluriSTEM Human ES/iPS Medium.
Stem Cell Research
Enzymes & Biochemistry
Quality
Physical form
Dispase-II enzyme is produced in Bacillus polymyxa.
Storage and Stability
Legal Information
Disclaimer
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
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Protocols
Stem cell reprogramming protocols to generate human induced pluripotent stem cells (iPSCs) including viral and non-viral RNA based methods.
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