Phase contrast image of an iPSC colony.

iPSC Generation

Immunofluorescence staining of patient specific iPSCs.

Stem Cell Characterization and Cell Line Quality Control

Immunofluorescence staining of a patient specific induced motor neuron markers.

CRISPR and TALEN Mediated Genome Editing

IF imaging of a group of induced motor neurons.

CRISPR Library Screening

Overview

The UCLA Stem Cell Engineering Center offers stem cell generation and editing services for research and industrial purposes. Our services aim to provide researchers with the tools they need to study the complexities of the human body and develop innovative therapies.

Our stem cell generation services involve the creation of induced pluripotent stem cells (iPSCs) from various cell types, including skin cells and blood cells. These iPSCs can be used to generate different types of cells for research, including neurons, heart cells, and liver cells.

We offer stem cell editing services using advanced CRISPR-Cas technologies. This allows researchers to edit specific genes in stem cells, creating disease models for studying genetic disorders and developing gene therapies.

Our Services

iPSC Generation

Reprogramming by Sendai Virus
Reprogramming by Episomal Vectors

Stem Cell Characterization and Cell Line Quality Control

Copy Number Variation Analysis
Pluripotency Marker IF Staining
Test of Pluripotency

CRISPR and TALEN Mediated Gene Editing

Gene Knock-In
Gene Knock-Out
Gene Correction
Gene Insertion
Reporter Cell Line Generation
CRISPR Screen Ready Cell Line Generation

 

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Our team of experts is dedicated to providing high-quality and reliable services to our clients. We use the latest techniques and technologies to ensure that our stem cells are of the highest quality and purity, and that our editing services are precise and efficient.

Order Through UCLA PPMS

Acknowledgement of Our Services

For submitting manuscripts that have made use of services or resources from this center, please acknowledge support by inclusion of the following information:

This work was supported by the UCLA Dr. Allen and Charlotte Ginsburg Center for Precision Genomic Medicine.

Please link each publication stemming from work performed in the center to your MyNCBI account. This will ensure that the contributions from NIH are appropriately acknowledged in renewal and continuation applications. This NIH requirement must be satisfied as part of our efforts to provide consistent access to stabling funded center resources.