Culturing Transcriptomically Distinct Pluripotent mESCs

This is intended as a guide only; for full experimental details please read the reference provided.

Kolodziejczyk et al. describe a protocol that uses two different cocktails of small molecules to maintain heterogeneous populations of mESCs with different metabolisms. STO feeder cells were used for mESC maintenance.

The use of 2i medium results in a heterogeneous population of blastocyst-like cells with a stable or ‘ground state’ of pluripotency. Alternative 2i (a2i) medium also results in a heterogeneous population of blastocyst-like cells with a stable or ‘ground state’ of pluripotency, which is transcriptomically distinct from that obtained with 2i medium.  A subpopulation of 2C-like cells is present with 2i medium. No differentiating cells are observed with either 2i or a2i.

https://resources.tocris.com/images/protocols/stemcells-image-2.jpg

Cocktails

Serum-containing Medium 2i Medium a2i Medium
DMEM   N2B27   N2B27  
1X Pen/Strep   CHIR 99021 (Cat.No. 4423) 3 μM CHIR 99021 (Cat.No. 4423) 3 μM
15% FBS   PD 0325901 (Cat.No. 4192) 1 μM CGP 77675  
Beta-Mercaptoethanol 0.1 mM rhLIF 100 U/ml rhLIF 100 U/ml
rhLIF 100 U/ml        
https://resources.tocris.com/images/protocols/stemcells-image-5.jpg

Reference

Kolodziejczyk et al. (2015) Single cell RNA-sequencing of pluripotent states unlocks modular transcriptional variation. Cell Stem Cell 17 471. PMID: 26431182

View Related Products

Stem Cell Proliferation


Related products from our sister brands