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Induced Pluripotent Stem Cells (iPSC) Services

Overview Service Features FAQs Scientific Resources Related Services

Overview

At Creative Biolabs, we enhance your research and data relevancy by acquiring and reprogramming induced pluripotent stem cells (iPSC) from a specific patient clinical profile. Our pipeline is designed to meet the clients' project and specific assay requirements for cellular characteristics and functions.

iPSC Reprogramming Service

Direct reprogramming of somatic cells into induced pluripotent stem (iPS) cells is a valuable method to produce patient-specific stem cells of any lineage without the use of embryonic materials. Various new strategies have been developed to improve the reprogramming technologies since the first report of iPS cells generation from murine fibroblasts using retroviral transduction of a defined set of transcription factors. Methods of factor reprogramming fall into two broad categories: chemical and transgene reprogramming. It has been reported that many small molecules promote reprogramming when used with classical reprogramming factors. Creative Biolabs has developed streamed-line protocols for efficient iPSC generation with viral vectors, DNA (plasmid), RNA and recombinant proteins. Each of our services will be provided with a comprehensive report suitable for publications.

  • Retrovirus vector
  • Lentivirus vector
  • Adenovirus vector
  • Sendai virus vector
  • PiggyBac transposon vector
  • Episomal plasmid vector
  • Direct delivery of synthetic mRNAs.
  • Mature double-stranded miRNAs
  • Factor Delivery by Protein

The primary factors to consider when deciding on a reprogramming method to generate iPSCs are what cell is being reprogrammed, the ability of the reprogramming method to adequately reprogram this cell type, as well as whether the presence of integrated sequences in the iPSCs will hinder downstream application.

The current reprogramming strategies used to induce pluripotent stem cells from adult somatic cells.Fig.1 The current reprogramming strategies used to induce pluripotent stem cells from adult somatic cells. (Lai, 2011)

iPSC Culture Service

Creative Biolabs is a worldwide leader in cell culture, including inducible cell line generation, and induced pluripotent stem cells culture. Creative Biolabs provides IPSC maintenance services and large-scale pluripotent cell production in both 2D and 3D formats. Based on our expertise in cell and stem cell biology, scientists at Creative Biolabs have developed unique media that are indispensable for iPSC research. Moreover, special products associated with advanced cell culture have been successfully established to help solve the problem involved in daily culture work, including mycoplasma detection kits and BacAway contamination control agents.

Pluripotency Characterization Service

Technological advances have made it increasingly easy to generate iPSC, but the characteristics of the various lines produced may vary depending on their source, derivation, passage number and culture conditions. To confirm the pluripotency, quality, identity, and safety of the pluripotent cell lines as they are derived and maintained, it is essential to perform a set of characterization analyses. Our assay development is led by scientists with extensive experience in pluripotency characterization. Working seamlessly with our iPSC generation, genome editing and cell differentiation resources, our assay development teams provides a fully integrated service to customers wishing to become the leaders of the iPSC-based drug discovery field.

iPSC Genome Editing Service

Creative Biolabs provides custom genome editing services in human cells, including cell lines and patient-derived cells. Although genome editing is not available for many somatic cell types, our iPSC-based services can be flexibly tailored to your needs through genome editing.

  • Gene knock-out
  • Gene insertion
  • Gene mutation
  • Gene correction or replacement
  • Inducible gene expression/ gene overexpression models

iPSC Differentiation Service

Creative Biolabs has extensive expertise in iPSC differentiation and can provide the most flexible, adaptable, and customizable solutions for your project. Different cell types are available, such as hepatocytes, cardiomyocytes, and neural cells. Other services include qRT-PCR of pluripotency genes, karyotyping for assessing genomic stability, and tri-lineage differentiation for assessing pluripotency in vitro.

Schematic overview of approaches to 1) differentiate smooth muscle cells (SMC) from induced pluripotent stem cells (iPSC), 2) use SMC to model vascular diseases, and 3) modulate cellular function through different microenvironmental cues.Fig.2 Schematic overview of approaches to 1) differentiate smooth muscle cells (SMC) from induced pluripotent stem cells (iPSC), 2) use SMC to model vascular diseases, and 3) modulate cellular function through different microenvironmental cues. (Ji, 2017)

Features of Our Services

With our offerings, we aim to empower researchers with versatile, reliable, and high-quality solutions that can streamline stem cell-based studies, increase the precision and accuracy of results, and speed up the scientific discovery process.

By partnering with our prestigious iPSC service, you will gain the following research advantages.

  • Robust and scalable technology - Our cutting-edge technology, built upon years of rigorous research, provides a robust and scalable platform for iPSC generation and differentiation.
  • Custom iPSC service - Bespoke services include iPSCs that are HLA-typed, genome-edited, or reporter line-engineered, catering to the diverse needs of various research projects.
  • Skillful scientific team - Our team of seasoned scientists brings years of experience in stem cell technology. They provide technical guidance at every step to optimize the utilization of our iPSC services.
  • Highly efficient - Our standardized procedures ensure batch-to-batch consistency and reliability, while the scalability allows high-throughput analyses.
  • Rigorous quality control protocols - Our iPSCs are thoroughly characterized using multiple stringent quality control measures. With strict adherence to international standards, we guarantee the purity, health, and viability of our products.
  • Low cost and timely submission - Our competitively priced iPSC services offer great value without compromising on quality. 
  • One-stop pipeline - We are committed to delivering unparalleled customer service, assisting you from project initiation to data interpretation.
  • Best after-sale service - Offering robust after-sales support, we stand by our iPSC services and products. Our dedicated scientific support team is just a call or email away, ready to answer any questions and troubleshoot any issues you may encounter.

Demonstrate your commitment to advancing scientific discovery in stem cells by partnering with our prestigious iPSC service. We are eager to connect with you and explore the vast potential of iPSC technology in your research.

Process and Timeline

With world-class expertise in the derivation, bioprocess scale-up, and differentiation of induced human pluripotent stem cells, our services team can finish the iPSC projects and provide pluripotent stem cells to you in as little as 16-24 weeks. The actual timelines will vary depending on the type of cell provided, the choice of iPSC technology and the choice of other alternative characterization services.

The potentials of iPS cell technology in cell-based therapies, reproductive medicine, and biomedical research are too great to ignore. Proper reprogramming strategies are critical to creating patient- and disease-specific stem cells which can be used in regenerative medicine. Creative Biolabs' stem cell program offers world-class expertise in the generation, bioprocess scale-up, and differentiation of iPSCs and uses this to provide solutions for your iPSC needs. Contact us today to discuss your iPSC project with a technical specialist.

FAQs

  • Q: How are the developed iPSCs typically delivered to clients?
    A: iPSCs can be delivered as a frozen vial of cells, or depending on the service, the cells could be further processed into desired cell types or tissues before delivery.
  • Q: How is the quality of iPSCs ensured in your ervices?
    A: Our quality assurance usually involves rigorous testing at each stage of the process, including testing for sterility, endotoxin levels, mycoplasma contamination and validation of pluripotency and functionality of the generated iPSCs.
  • Q: Can iPSC services be customized to specific research needs?
    A: Yes, we offer customizable iPSC services to cater to the specific needs of a research project.
  • Q: What services are offered under iPSC services?
    A: Our services typically include iPSC generation, iPSC differentiation into various cell types, genome editing in iPSCs, and development of disease models using iPSCs among others.
  • Q: What cell types can be reprogrammed into iPSCs?
    A: Almost any type of somatic cell can be reprogrammed into iPSCs, most commonly skin cells and blood cells are used.
  • Q: What is the turnaround time for iPSC services?
    A: The precise turnaround time can vary widely depending on the exact service. For instance, generation of iPSC lines may take several weeks to a few months.
  • Q: How are iPSCs validated?
    A: iPSCs are typically validated through a series of tests including pluripotency assay, differentiation potential, karyotyping for genome stability, and marker expression.
  • Q: How much does iPSC service cost?
    A: The cost of iPSC services can vary widely, depending on what is included in the service package, such as the source of cells, the number of clonal cell lines required, and any additional characterization or differentiation services.

Scientific Resources

References

  1. Lai, M.I.; et al. Advancements in reprogramming strategies for the generation of induced pluripotent stem cells. J Assist Reprod Genet. 2011, 28(4): 291-301.
  2. Ji, H.; et al. Application of induced pluripotent stem cells to model smooth muscle cell function in vascular diseases. Curr Opin Biomed Eng. 2017, 1: 38-44.

For Research Use Only. Not For Clinical Use.