For researchers working with human and mouse pluripotent stem cells (PSCs), reliable feeder-dependent culture systems are important for maintaining pluripotency, reproducibility, and scalability. The Gibco KnockOut Media family offers a solution—cited in thousands of peer-reviewed publications—for feeder-based PSC workflows. Built on defined formulations and rigorously tested performance, KnockOut products help enable robust PSC maintenance, differentiation, and derivation.

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Choose the Gibco KnockOut products that best fit your stem cell culture needs

ProductKnockOut Serum Replacement (KSR)

KnockOut DMEM

KnockOut DMEM/F-12

ApplicationFeeder-dependent PSC cultureFeeder-dependent PSC cultureNeural stem cell culture
Benefits
  • A defined substitute for serum, meant for the culture of ESCs and iPSCs
  • Cited in over 2,000 publications for various PSC-related applications
  • Helps to reduce the burden of qualifying reagents when transitioning to clinical applications
  • A chemically defined basal medium designed for ESCs and iPSCs
  • Mimics the low-osmolality environment of mouse embryonic tissues
  • Reduces PSC differentiation, especially when used with KnockOut SR – Multi-Species
  • A chemically defined, low-osmolality basal medium without HEPES buffer
  • Supports expansion and differentiation of neural stem cells
  • Maintains human ESCs and iPSCs with normal morphology and karyotype
CTS versionCTS KnockOut SR XenoFree MediumCTS KnockOut DMEMCTS KnockOut DMEM/F-12

KnockOut media resources


Publications
  1. Guo G, Pinello L, Han X, et al. (2016) Serum-based culture conditions provoke gene expression variability in mouse embryonic stem cells as revealed by single-cell analysis. Cell Reports 14(4):956–965. doi:10.1016/j.celrep.2015.12.089
  2. Sundberg M, Bogetofte H, Lawson T, et al. (2013) Improved cell therapy protocols for Parkinson's disease based on differentiation efficiency and safety of hESC-, hiPSC-, and non-human primate iPSC-derived dopaminergic neurons. Stem Cells 31(8):1548–1562. doi:10.1002/stem.141
  3. Liu J, Koscielska KA, Cao Z, et al. (2012) Signaling defects in iPSC-derived fragile X premutation neurons. Human Molecular Genetics 21(17):3795–3805. doi:10.1093/hmg/dds207
  4. Davies TJ, Fairchild PJ (2012) Optimization of protocols for derivation of mouse embryonic stem cell lines from refractory strains, including the non-obese diabetic mouse. Stem Cells and Development 21(10):1688–1700. doi:10.1089/scd.2011.042
  5. Ef Hirai H, Katoku-Kikyo N, Karian P, et al. (2012) Efficient iPS cell production with the MyoD transactivation domain in serum-free culture. PLoS One 7(3):e34149. doi:10.1371/journal.pone.003414
  6. Wang A, Tang Z, Park IH, et al. (2011) Induced pluripotent stem cells for neural tissue engineering. Biomaterials 32(22):5023–5032. doi:10.1016/j.biomaterials.2011.03.070
  7. Hamanaka S, Yamaguchi T, Kobayashi T, et al. (2011) Generation of germline-competent rat induced pluripotent stem cells. PLoS One 6(7):e22008. doi:10.1371/journal.pone.0022008
  8. Koh KP, Yabuuchi A, Rao S, et al. (2011) Tet1 and Tet2 regulate 5-hydroxymethylcytosine production and cell lineage specification in mouse embryonic stem cells. Cell Stem Cell 8(2):200–213. doi:10.1016/j.stem.2011.01.008
  9. Li Y, Cang M, Lee AS, et al. (2011) Reprogramming of sheep fibroblasts into pluripotency under a drug-inducible expression of mouse-derived defined factors. PLoS One 6(1):e15947. doi:10.1371/journal.pone.0015947
  10. Zhang N, An MC, Montoro D, et al. (2010) Characterization of human Huntington's disease cell model from induced pluripotent stem cells. PLoS Currents 2:RRN1193. doi:10.1371/currents.RRN1193
  11. Li L, Fukunaga-Kalabis M, Yu H, et al. (2010) Human dermal stem cells differentiate into functional epidermal melanocytes. Journal of Cell Science 123(Pt 6):853–860. doi:10.1242/jcs.061598
  12. Zhao XY, Li W, Lv Z, et al.(2010) Efficient and rapid generation of induced pluripotent stem cells using an alternative culture medium. Cell Res 20(3):383–386. doi: 10.1038/cr.2010.26
  13. Li W, Ding S (2010) Generation of novel rat and human pluripotent stem cells by reprogramming and chemical approaches. Methods Mol Biol 636:293–300. doi: 10.1007/978-1-60761-691-7_18

For Research Use Only. Not for use in diagnostic procedures.

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