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Home -> Cell Biology -> Stem Cell related Products -> Human Induced Pluripotent Cells (Human iPS Cell Lines)

Human Induced Pluripotent Cells (Human iPS Cell Lines)

Jump start your iPS cell research with pre-made, high quality iPS cell lines

iPS cell lines made using Oct4, Sox2, c-Myc, and KLF4
Study the induced pluripotency process
Measure mRNA and microRNA signatures
Identify novel epigenetic markers to study pattern formation
Develop directed differentiation protocols


All iPS Cell lines are certified to be pluripotent through iPS Cell Marker staining

Image

Stem cell markers for SSEA4/1 and Nanog were determined by immunocytochemistry using primary antibodies for SSEA1 (Millipore), SSEA4 (Abcam) and Nanog (Abcam) followed by fluorescent-labeled secondary Alexa594 antibodies (Invitrogen). Detection of Alkaline Phosphatase activity was performed using the AP Detection kit (Millipore). Teratoma assays were performed by subcutaneous injection of 1x10^6 iPS cells into the dorsal flank of SCID mice. Teratomas were visualized after 4 weeks with hematoxylin and eosin staining.


Custom iPS Cell Line Service
Provide cells from your human or mouse model system, and our partner SBI will reprogram the cells using lentivirus expressing Oct4, Sox2, Klf4, and c-myc.
After about 3 months you will receive your specific iPS Cell Line, certified to be pluripotent through marker staining. Please see link below to request a quotation.


Related Links

StemPure Growth Medium
Mouse iPS Cell Line
Ask for a Custom iPS Cell Line Service Quotation
Overview of Tools for Stem Cell Research


 

Description Cat# Size Price    
Human Adipose Stem Cell-derived (feeder-free) iPS cells (hASC-iPSCs) SC402A-1-GVO-SBI 2 x 10e5 cells 1242 € DETAILS Order
Human Fibroblast-derived (feeder-free) iPSC Cell Line SC102A-1-GVO-SBI 2 x 10e5 cells 1219 € DETAILS Order

 


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Fluorescent Protein Vectors

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Lentiviral-based barcode library

Track clonal populations of cells over time or through different treatments using the lentiviral-based barcode library.

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