ReproTeSR™ Medium for Reprogramming (2-Component)

Reprogramming medium for human iPS cell induction
概要

ReproTeSR™ (2-Component) is a complete and xeno-free reprogramming medium developed for generating human induced pluripotent stem (iPS) cells from fibroblasts, urine-derived cells, and blood-derived cells such as CD34+ or erythroid precursor cells under feeder-free conditions.

ReproTeSR™ is also available as part of an integrated set of tools that are optimized for reprogramming blood-derived cell types expanded in vitro from peripheral blood, such as CD34+ cells (CD34+ Progenitor Reprogramming Kit, Catalog #05925) or erythroid cells (Erythroid Progenitor Reprogramming Kit, Catalog #05924).

Advantages
• Defined, feeder-free formulation facilitates reproducibly efficient human iPS cell generation
• Rapid emergence of large colonies with high-quality iPS cell-like morphology facilitates identification and subcloning for easily establishing iPS cell lines
• Seamlessly integrates with STEMCELL products prior to reprogramming and after iPS cell generation for maintenance and differentiation
Components
TeSR™-E7™/ReproTeSR™ Basal Medium, 480 mL
ReproTeSR™ 25X Supplement, 20 mL
 
Subtype
专业培养基
Cell Type
多能干细胞, 造血干细胞和祖细胞
Species
Application
细胞培养, 重编程
Brand
TeSR
Area of Interest
干细胞生物学
Formulation
无血清, 无异种成分


技术资料

Scientific Resources

相关产品

Educational Materials (8)

产品宣传册
Maximize Your Pluripotential with the TeSR™ Family of hPSC Culture Media
Maximize Your Pluripotential with the TeSR™ Family of hPSC Culture Media
产品宣传册
血细胞重编程的完整流程
血细胞重编程的完整流程
产品宣传册
人多能干细胞 相关产品
人多能干细胞 相关产品
技术公告
使用游离性载体系统,在TeSR™-E7™ 或ReproTeSR™中将人尿液衍生细胞重编程为诱导多能干(iPS)细胞
使用游离性载体系统,在TeSR™-E7™ 或ReproTeSR™中将人尿液衍生细胞重编程为诱导多能干(iPS)细胞
数据及文献

Product Applications

This product is designed for use in the following research area(s) as part of the highlighted workflow stage(s). Explore these workflows to learn more about the other products we offer to support each research area.

Data and Publications

数据

Figure 1. Blood Cell Reprogramming Efficiencies Are Higher in ReproTeSR™ Medium Compared to in hESC Medium

Efficiency of reprogramming (A) erythroid cells or (B) CD34+ cells using episomal reprogramming vectors is higher in ReproTeSR™ medium compared to in KOSR-containing hESC medium. Data shown are mean /- SEM; erythroid cells, n=4; CD34 cells, n=5.

Figure 2. ReproTeSR™ Efficiently Reprograms Fibroblasts

Dermal fibroblasts were transfected with the ReproRNA™-OKSGM vector and reprogrammed under feeder-dependent (standard KOSR-containing hES cell medium on inactivated mouse embryonic fibroblasts (iMEFs)) or feeder-independent conditions (ReproTeSR™ on Corning® Matrigel®). Fibroblasts (passage 4) were reprogrammed with average efficiencies of 0.10 ± 0.06% (hES cell medium) and 0.20 ± 0.07% (ReproTeSR™). Reprogramming efficiency of fibroblasts with ReproRNA™ and ReproTeSR™ is comparable to that reported with Sendai virus. (Schlaeger TM, et al. (2015) Nat Biotechnol 33(1): 58-63.) (n ≥ 6; Data shown are mean ± SD).

Figure 3. Feeder-Free Reprogramming with ReproRNA™-OKSGM Vector and ReproTeSR™ Generates iPS Cell Colonies with Superior Colony Morphology

Representative images of iPS cell colonies were generated using ReproRNA™‑OKSGM and cultured in (A) standard hES cell medium on irradiated mouse embryonic fibroblasts (iMEFs) or (B) ReproTeSR™ on Corning® Matrigel®. iPS cell colonies derived using ReproTeSR™ exhibit more defined borders, compact morphology, and reduced differentiation as compared to the ES cell medium.


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