- You are here: Home
- Applications
- Oncology
- Model-based Drug Screening
- Humanized-Xenograft Model-based Drug Screening
- iPS Cell Research
Applications
-
Cell Services
- Cell Line Authentication
- Cell Surface Marker Validation Service
-
Cell Line Testing and Assays
- Toxicology Assay
- Drug-Resistant Cell Models
- Cell Viability Assays
- Cell Proliferation Assays
- Cell Migration Assays
- Soft Agar Colony Formation Assay Service
- SRB Assay
- Cell Apoptosis Assays
- Cell Cycle Assays
- Cell Angiogenesis Assays
- DNA/RNA Extraction
- Custom Cell & Tissue Lysate Service
- Cellular Phosphorylation Assays
- Stability Testing
- Sterility Testing
- Endotoxin Detection and Removal
- Phagocytosis Assays
- Cell-Based Screening and Profiling Services
- 3D-Based Services
- Custom Cell Services
- Cell-based LNP Evaluation
-
Stem Cell Research
- iPSC Generation
- iPSC Characterization
-
iPSC Differentiation
- Neural Stem Cells Differentiation Service from iPSC
- Astrocyte Differentiation Service from iPSC
- Retinal Pigment Epithelium (RPE) Differentiation Service from iPSC
- Cardiomyocyte Differentiation Service from iPSC
- T Cell, NK Cell Differentiation Service from iPSC
- Hepatocyte Differentiation Service from iPSC
- Beta Cell Differentiation Service from iPSC
- Brain Organoid Differentiation Service from iPSC
- Cardiac Organoid Differentiation Service from iPSC
- Kidney Organoid Differentiation Service from iPSC
- GABAnergic Neuron Differentiation Service from iPSC
- Undifferentiated iPSC Detection
- iPSC Gene Editing
- iPSC Expanding Service
- MSC Services
- Stem Cell Assay Development and Screening
- Cell Immortalization
-
ISH/FISH Services
- In Situ Hybridization (ISH) & RNAscope Service
- Fluorescent In Situ Hybridization
- FISH Probe Design, Synthesis and Testing Service
-
FISH Applications
- Multicolor FISH (M-FISH) Analysis
- Chromosome Analysis of ES and iPS Cells
- RNA FISH in Plant Service
- Mouse Model and PDX Analysis (FISH)
- Cell Transplantation Analysis (FISH)
- In Situ Detection of CAR-T Cells & Oncolytic Viruses
- CAR-T/CAR-NK Target Assessment Service (ISH)
- ImmunoFISH Analysis (FISH+IHC)
- Splice Variant Analysis (FISH)
- Telomere Length Analysis (Q-FISH)
- Telomere Length Analysis (qPCR assay)
- FISH Analysis of Microorganisms
- Neoplasms FISH Analysis
- CARD-FISH for Environmental Microorganisms (FISH)
- FISH Quality Control Services
- QuantiGene Plex Assay
- Circulating Tumor Cell (CTC) FISH
- mtRNA Analysis (FISH)
- In Situ Detection of Chemokines/Cytokines
- In Situ Detection of Virus
- Transgene Mapping (FISH)
- Transgene Mapping (Locus Amplification & Sequencing)
- Stable Cell Line Genetic Stability Testing
- Genetic Stability Testing (Locus Amplification & Sequencing + ddPCR)
- Clonality Analysis Service (FISH)
- Karyotyping (G-banded) Service
- Animal Chromosome Analysis (G-banded) Service
- AAV Biodistribution Analysis (RNA ISH)
- Molecular Karyotyping (aCGH)
- Droplet Digital PCR (ddPCR) Service
- Digital ISH Image Quantification and Statistical Analysis
- SCE (Sister Chromatid Exchange) Analysis
- Biosample Services
- Histology Services
- Exosome Research Services
- In Vitro DMPK Services
-
In Vivo DMPK Services
- Pharmacokinetic and Toxicokinetic
- PK/PD Biomarker Analysis
- Bioavailability and Bioequivalence
- Bioanalytical Package
- Metabolite Profiling and Identification
- In Vivo Toxicity Study
- Mass Balance, Excretion and Expired Air Collection
- Administration Routes and Biofluid Sampling
- Quantitative Tissue Distribution
- Target Tissue Exposure
- In Vivo Blood-Brain-Barrier Assay
- Drug Toxicity Services
iPS Cell Research
Creative Bioarray provides a comprehensive cell biological research for global customers including cell line tests, stem cell research and induced pluripotent stem cell (iPS cell) research. Our intelligent experts and platform perform perfectly in iPS cell research. We can provide sufficient assistance to adjust your research and meet the project needs. And our company sustains a leader in the changing research environment.
What Is iPS Cell?
Induced pluripotent stem cells (also known as iPS cells or iPSCs) are a kind of pluripotent stem cell which can be extracted directly from adult cells. This iPSC technology was first developed in 2006 by Shinya Yamanaka’s lab in Kyoto, Japan, and showing that the introduction of four specific genes encoding transcription factors could convert adult cells into pluripotent stem cells. In past periods of regenerative medicine, the embryonic stem cell is the most well-known type of pluripotent stem cell. However, the generation of embryonic stem cells involves destruction (or at least manipulation) of the pre-implantation stage embryo. Further, since embryonic stem cells can only be derived from embryos, there has been much controversy surrounding their use. On the contrary, iPS cells can be derived directly from adult tissues, they not only bypass the need for embryos, but can be made in a patient-matched manner, which means that each individual could have their own pluripotent stem cell line.
How Can We Produce iPS Cells?
iPS cells are typically derived by introducing products of specific sets of pluripotency-associated genes, or "reprogramming factors" such as Oct4 (Pou5f1), Sox2, cMyc, and Klf4, into a given cell type. While this combination of the transcription factors is most conventional in producing iPSCs, each of the factors can be functionally replaced by related transcription factors, miRNAs, small molecules, or even non-related genes such as lineage specifiers.
Figure 1. A process of the generation of induced pluripotent stem (IPS) cells. (1) Isolate and culture donor cells from tissue, blood or organ. (2) Trans stem cell-associated genes into the cells by viral vectors. The cells expressing the exogenous genes are in red. (3) Harvest and culture the cells according to ES cell culture. (4) A small subset of the transfected cells generates ES-like colonies which become iPS cells at last.
The process of iPS cell derivation is typically slow and inefficient. It will take 1–2 weeks for mouse cells and 3–4 weeks for human cells, with efficiency around 0.01%–0.1%. With the development of technology, considerable advances have been made in improving the efficiency to obtain iPS cells. Upon introduction of reprogramming factors, cells begin to form colonies that resemble pluripotent stem cells, which can be isolated based on their morphology, conditions that select for their growth, or through expression of surface markers & reporter genes.
iPS Cell Research at Creative Bioarray
We provide a broad range of cell-reprogramming technique systems, including mRNA reprogramming, dox-inducible human 4F2A reprogramming and lentivirus reprogramming for our customers to develop iPSC lines and further assays.
Our researches working hard to produce iPS cell related products, such as iPSC factor proteins, iPSC medium & culture reagents, iPSC related cells and so on. We have built up expertise in differentiation of high purity, functional cell types.
CRISPR/Cas9 System for iPS Cells
We use the CRISPR/Cas9 gene-editing tool, which has gained huge popularity in recent years, to create a RNA-guided site-specific DNA cleavage and introduce disease-associated mutations into a sample of iPS cells.
Creative Bioarray provides a portfolio of flexible and integrated solutions for iPS cell research. Quality management system, complete data conservation and process audits trails all guarantee the data reliable. We are looking forward to being a long-term partner with you.
Reference
- Takahashi, K.; et al. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell. 2006, 126(4): 663–76.
Explore Other Options
For research use only. Not for any other purpose.