Cell cryopreservation composition and application thereof
A composition and cell technology, applied in the field of cells, can solve the problems of poor cell survival rate and achieve the effect of improving survival rate, shortening cycle and reducing cost
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] (1) Cell cryopreservation:
[0035] Freezing solution formula:
[0036]
[0037] 1. Prepare cell freezing culture medium, the formula used is DMEM+20%FBS+10%DMSO+50ug / ml antifreeze protein (extracted from winter wheat plant)
[0038] 2. Take the cells in the logarithmic growth phase, remove the old culture medium, and wash with PBS.
[0039] 3. Remove the PBS, add an appropriate amount of trypsin (covering the surface of the culture dish) to digest the cells growing in a single layer;
[0040] 4. Centrifuge at 1000rpm for 5min;
[0041] 5. Remove trypsin, add an appropriate amount of prepared frozen culture medium, blow gently with a pipette to make the cells uniform, count, and adjust the final density of cells in the frozen medium to 5×106 / ml~1×107 / ml;
[0042] 6. Divide the cells into cryopreservation tubes, 1-1.5ml per tube;
[0043] 7. Mark the name of the cells, the time of freezing and the operator on the cryopreservation tube;
[0044] 8. Cryopreservation:...
Embodiment 2
[0052] (1) Cell cryopreservation:
[0053] Freezing solution formula:
[0054]
[0055] 1. Prepare cell freezing culture medium, the formula used is DMEM+20%FBS+10%DMSO+50ug / ml antifreeze protein (extracted from winter wheat plant)
[0056] 2. Take the cells in the logarithmic growth phase, remove the old culture medium, and wash with PBS.
[0057] 3. Remove the PBS, add an appropriate amount of trypsin (covering the surface of the culture dish) to digest the cells growing in a single layer;
[0058] 4. Centrifuge at 1000rpm for 5min;
[0059] 5. Remove trypsin, add an appropriate amount of prepared frozen culture medium, blow gently with a pipette to make the cells uniform, count, and adjust the final density of cells in the frozen medium to 5×106 / ml~1×107 / ml;
[0060] 6. Divide the cells into cryopreservation tubes, 1-1.5ml per tube;
[0061] 7. Mark the name of the cells, the time of freezing and the operator on the cryopreservation tube;
[0062] 8. Cryopreservatio...
Embodiment 3
[0070] (1) Cell cryopreservation:
[0071] Freezing solution formula:
[0072]
[0073] 1. Prepare cell freezing culture medium, the formula used is DMEM+20%FBS+10%DMSO+50ug / ml antifreeze protein (extracted from winter wheat plant)
[0074] 2. Take the cells in the logarithmic growth phase, remove the old culture medium, and wash with PBS.
[0075] 3. Remove the PBS, add an appropriate amount of trypsin (covering the surface of the culture dish) to digest the cells growing in a single layer;
[0076] 4. Centrifuge at 1000rpm for 5min;
[0077] 5. Remove trypsin, add an appropriate amount of prepared frozen culture medium, blow gently with a pipette to make the cells uniform, count, and adjust the final density of cells in the frozen medium to 5×106 / ml~1×107 / ml;
[0078] 6. Divide the cells into cryopreservation tubes, 1-1.5ml per tube;
[0079] 7. Mark the name of the cells, the time of freezing and the operator on the cryopreservation tube;
[0080] 8. Cryopreservatio...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com