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Human iPS Cell Line (Normal)

SKU: 30HU-002

Human iPS Cell Line (Normal)

SKU: 30HU-002
Pricing Starting at

Starting at: $1,586.00

Available Options

SKUPackage SizePriceQuantityAdd to Cart
30HU-002Cryopreserved, 0.5-1.0 million cells/vialStarting at: $1,586.00

Associated Products

Description

Product Description

Induced Pluripotent Stem Cells (iPSCs) are a type of stem cells generated by reprogramming a variety of mature, specialized somatic cells into an embryonic-like pluripotent state. iPSCs exhibit large self-renewal capability and can differentiate into cells from all three germ layers [1, 2]. Due to their high differentiation potential, iPSC serves as a unique cell model for the regenerative medicine. In addition, iPSCs reprogrammed from rare disease carriers can be expanded and differentiated into specific cell types, allowing research with genetically pertinent disease-specific cell models for personalized treatment [3]. iPSCs, thus, provide a unique model for studying a variety of processes that occur in the early development and become a promising tool in cell therapy of human diseases [4].

iXCells Biotechnologies is proud to offer human iPSCs derived from normal and patient somatic cells (dermal fibroblasts or peripheral blood mononuclear cells) with different race, gender, and age options to choose from. The pertinent donor information is available on the CoA or upon request ([email protected]). These iPSCs are established from single clones and expanded in feeder-free conditions. iXCells’ iPSCs demonstrate hESC morphology, express pluripotency markers, have normal karyotype, and are integration free (Figure 1). The iPSCs have been extensively used in differentiation projects to generate various cell types, including neurons, astrocytes, microglia, skeletal muscles, and hepatocytes (Figure 2). They are negative for mycoplasma, bacteria, yeast, fungi,HIV-1, HBV and HCV. In addition, patient-derived iPS cell lines are also available as separate products. The currently available disease specific iPS cell lines are derived from patients with Type 2 Diabetes (T2D; Cat#30HU-005), Alzheimer’s Disease (AD; Cat#30HU-008, Cat#30HU-009), Amyotrophic Lateral Sclerosis (ALS; Cat#30HU-004). More disease-specific iPS lines are under development. We also provide custom iPSC generation and iPSC differentiation services to meet your needs.

Figure 1. iXCells human iPS Cell Lines are characterized by immunostaining targeting Oct4, Nanog, TRA-1-60, and TRA-1-81. Images are also stained with DAPI to show cell nuclei. Scale bar = 100μm.

Figure 2. iXCells human iPS Cell Lines demonstrate a high capacity for differentiation into various cell types, including Neurons, Skeletal Muscles, and Astrocytes. Scale bar = 100μm.

Product Details

Organism  Homo Sapiens, Human
Tissue Origin  Dermal fibroblast or peripheral blood mononuclear cells
Cell Type  iPSC
Disease  Normal
Package Size  0.5-1.0 x 106cells/vial
Growth Properties  Adherent
Product Format/Shipped  Cryopreserved
Storage  Liquid Nitrogen
Associated Media Human iPSC Feeder-Free Growth Medium (Cat# MD-0019)

Human iPSC Xeno-Free Growth Medium (Cat# MD-0074)

References

[1] Medvedev, S. P., Shevchenko, A. I., & Zakian, S. M. (2010). Induced Pluripotent Stem Cells: Problems and Advantages when Applying them in Regenerative Medicine. Acta naturae, 2(2), 18–28.

[2] Ghaedi, M., & Niklason, L. E. (2019). Human Pluripotent Stem Cells (iPSC) Generation, Culture, and Differentiation to Lung Progenitor Cells. Methods in molecular biology (Clifton, N.J.), 1576, 55–92.

[3] Okita, K., Matsumura, Y., Sato, Y., Okada, A., Morizane, A., Okamoto, S., Hong, H., Nakagawa, M., Tanabe, K., Tezuka, K., Shibata, T., Kunisada, T., Takahashi, M., Takahashi, J., Saji, H., & Yamanaka, S. (2011). A more efficient method to generate integration-free human iPS cells. Nature methods, 8(5), 409–412.

[4] Ebert, A. D., Liang, P., & Wu, J. C. (2012). Induced pluripotent stem cells as a disease modeling and drug screening platform. Journal of cardiovascular pharmacology, 60(4), 408–416.

Datasheet & Culture Protocol

Datasheet & Culture Protocol

  • Dong, X., Chen, Y., Lu, J., Huang, S., & Pei, G. (2022). Β-arrestin 2 and EPAC2 cooperatively mediate DRD1-stimulated proliferation of human neural stem cells and growth of human cerebral organoids. Stem Cells. https://doi.org/10.1093/stmcls/sxac046 -- Learn More
  • Huang, M., Wang, X., Banerjee, M., Mukherji, S. T., Kutz, L. C., Zhao, A., Sepanski, M., Fan, C.-M., Zhu, G.-Z., Tian, J., Wang, D.-Z., Zhu, H., Xie, Z.-J., Pierre, S. V., & Cai, L. (2022). Regulation of myogenesis by a na/K-atpase α1 caveolin binding motif. Stem Cells. https://doi.org/10.1093/stmcls/sxab012 -- Learn More
  • Huang, S., Huang, F., Zhang, H., Yang, Y., Lu, J., Chen, J., Shen, L., & Pei, G. (2022). In vivo development and single‐cell transcriptome profiling of human brain organoids. Cell Proliferation. https://doi.org/10.1111/cpr.13201 -- Learn More
  • Wang, X., Cai, L., Xie, J. X., Cui, X., Zhang, J., Wang, J., . . . Xie, Z. (2020). A caveolin Binding motif in Na/K-ATPase is required for stem cell differentiation and organogenesis in mammals andc.elegans. Science Advances, 6(22). doi:10.1126/sciadv.aaw5851 -- Learn More

  • Hilary Sherman & Hannah J. Gitschier. (2019). A Novel Method for Generating Single, Intestinal Organoids for High Throughput Screening. Corning Application Note -- Learn More
  • Gasset-Rosa, F., Lu, S., Yu, H., Chen, C., Melamed, Z., Guo, L., . . . Cleveland, D. W. (2019). Cytoplasmic TDP-43 De-mixing independent of Stress Granules Drives inhibition of NUCLEAR IMPORT, loss of Nuclear TDP-43, and cell death. Neuron, 102(2). doi:10.1016/j.neuron.2019.02.038 -- Learn More
  • Gao, X., Sprando, R. L., & Yourick, J. J. (2018). A rapid and highly efficient method for the Isolation, purification, and Passaging of Human-Induced pluripotent stem cells. Cellular Reprogramming, 20(5), 282-288. doi:10.1089/cell.2018.0022 -- Learn More
  • Marei, H. E., Althani, A., Lashen, S., Cenciarelli, C., & Hasan, A. (2017). Genetically unmatched human Ipsc and Esc Exhibit Equivalent gene expression and neuronal differentiation potential. Scientific Reports, 7(1). doi:10.1038/s41598-017-17882-1 -- Learn More
  • Gao, X., Yourick, J. J., & Sprando, R. L. (2017). Comparative transcriptomic analysis of endothelial progenitor cells derived from umbilical cord blood and adult peripheral blood: Implications for the generation of induced pluripotent stem cells. Stem Cell Research, 25, 202-212. doi:10.1016/j.scr.2017.11.004 -- Learn More

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