Cookie Settings
We use cookies to provide the best possible website experience for you. This includes cookies that are technically required to ensure a proper functioning of the website, as well as cookies which are used solely for anonymous statistical purposes, for more comfortable website settings, or for displaying personalized content. You are free to choose the categories you would like to permit. Please note that depending on your settings, the full functionality of the website may no longer be available. Further information can be found in our Privacy Statement and Cookie Statement.
Mouse embryonic fibroblasts (mEF) were depleted from a co-culture with mouse embryonic stem (mES) cells using Feeder Removal MicroBeads, an LS Column, and a MidiMACS™ Separator. Flow cytometric analysis with CD15 (SSEA-1)-APC and Anti-Feeder-PE on the MACSQuant® Analyzer indicates that a starting population of 10% mEF was completely removed. The purity of the enriched mES cells was about 99.9%. |
Unseparated fraction | After separation |
Feeder Removal MicroBeads, mouseFigure 1Mouse embryonic fibroblasts (mEF) were depleted from a co-culture with mouse embryonic stem (mES) cells using Feeder Removal MicroBeads, an LS Column, and a MidiMACS™ Separator. Flow cytometric analysis with CD15 (SSEA-1)-APC and Anti-Feeder-PE on the MACSQuant® Analyzer indicates that a starting population of 10% mEF was completely removed. The purity of the enriched mES cells was about 99.9%. | Feeder Removal MicroBeads, mouseFigure 1Mouse embryonic fibroblasts (mEF) were depleted from a co-culture with mouse embryonic stem (mES) cells using Feeder Removal MicroBeads, an LS Column, and a MidiMACS™ Separator. Flow cytometric analysis with CD15 (SSEA-1)-APC and Anti-Feeder-PE on the MACSQuant® Analyzer indicates that a starting population of 10% mEF was completely removed. The purity of the enriched mES cells was about 99.9%. |
Mouse embryonic fibroblasts (mEF) were depleted from a co-culture with mouse embryonic stem (mES) cells using Feeder Removal MicroBeads, an LS Column, and a MidiMACS™ Separator. Flow cytometric analysis with CD15 (SSEA-1)-APC and Anti-Feeder-PE on the MACSQuant® Analyzer indicates that a starting population of 10% mEF was completely removed. The purity of the enriched mES cells was about 99.9%. |
Unseparated fraction | After separation |
Feeder Removal MicroBeads, mouseFigure 1Mouse embryonic fibroblasts (mEF) were depleted from a co-culture with mouse embryonic stem (mES) cells using Feeder Removal MicroBeads, an LS Column, and a MidiMACS™ Separator. Flow cytometric analysis with CD15 (SSEA-1)-APC and Anti-Feeder-PE on the MACSQuant® Analyzer indicates that a starting population of 10% mEF was completely removed. The purity of the enriched mES cells was about 99.9%. | Feeder Removal MicroBeads, mouseFigure 1Mouse embryonic fibroblasts (mEF) were depleted from a co-culture with mouse embryonic stem (mES) cells using Feeder Removal MicroBeads, an LS Column, and a MidiMACS™ Separator. Flow cytometric analysis with CD15 (SSEA-1)-APC and Anti-Feeder-PE on the MACSQuant® Analyzer indicates that a starting population of 10% mEF was completely removed. The purity of the enriched mES cells was about 99.9%. |
Seems like you are coming from USA!
Do you want to visit our website in your country?
Copyright © 2022 Miltenyi Biotec and/or its affiliates. All rights reserved.