Quality Reagents for Stable Growth Environments

Check out our new product, FGF2 DISCs!

FGF2 DISCs provide stable, defined levels of native FGF2 in cell culture medium. FGF2 DISCs are biocompatible hydrogels embedded with controlled-release FGF2 StemBeads®.

Reduce culture feeding frequency and media usage while also providing steady FGF2 release, which reduces cellular stress and enhances culture quality.

Or try StemBeads

StemBeads® are encapsulated proteins that provide a controlled release over the course of one week and integrate directly with the cell culture. Check out our product link to see what variations of StemBeads are available.

Featured Products

StemBeads technology is available for several different growth factors. Click the image here to see what we have available!

FGF2 DISCs are embedded with StemBeads and can be easily added and removed from culture. Click the image above to get some today!

Testimonials

I used the Stem Culture FGF2 beads on both a normal line and Swachman-Diamond Syndrome line of human iPS cells in my media over the weekend. I added iPS media with the Stem Culture FGF2 beads substituting for the FGF in my typical media on Friday, and by Monday my cultures still looked remarkably healthy. It’s so liberating to know there’s a product to relieve the weekend culture feeding!

Christine Miller,
Research Assistant Harvard University, Joslin Diabetes Center,
Amy Wagers Lab

The beads worked very well in my hands, I used for the last week end and did not observe any differentiation.

Salvatore Iovino,
Postdoctoral fellow Joslin Diabetes Center,
Ronald Kahn Lab

StemBeads worked beautifully on our cells. After 1 month of culturing in Stembeads, the hESC colonies remained nice and undifferentiated, and even seemed to grow faster than in conventional hESC media with bFGF. It’s excellent that we no longer need to come in to change medium during the weekends.

Agnette Kirkeby,
Postdoctoral Fellow Lund University,
Anders Bjorklund Lab

In my hands, StemBeads work very well, even when cells are cultured on matrigel in using TESR. I have been feeding my cells very 3 days, and the look at least as good, if not better than cells fed every day without StemBeads. This allows me to take care of more cell lines at once, and to spend more time doing things besides routine tissue culture.

Maureen Sherry Lynes, 
Post-Doctoral Fellow Harvard Stem Cell Institute, 
Lee Rubin Lab

I am an Assistant Professor in Johns Hopkins University, School of Medicine. I have extensive experience of culturing human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs) more than 7 years now. Luckily my lab had a chance to test FGF2 Beads for maintaining hESCs and hiPSCs. FGF2- beads showed successful results. Whenever I met someone who wants to start any research with hESCs and hiPSCs, they are worrying about tissue culture. Indeed these cells need very special care. One of the issues is that these cells should be fed everyday, which compromises several things, including work hours during weekend and holiday season, wasting expensive culture media and increasing chances of contamination. But the FGF2-beads can solve these issues and should be very attractive choice for the researchers who are working on these particular cell types.

Gabsang Lee, 
Ph.D., D.V.M., 
Assistant Professor Johns Hopkins University School of Medicine

We choose StemBeads FGF2 in order to use in combination with cell surface marker antibody for live cell immunostaining, and we have been very pleased with the product:
Stembeads FGF2 are stable with good quality, the beads gradually release FGF2 into the cell culture medium, which allow us to finish the assays in a 2-3 days timeframe without medium change.

Monica Zhou, 
Staff Scientist New York Stem Cell Foundation

The StemBeads FGF2 worked really well in my hands. They allowed me to change the media every 3 or 4 days without any problems with differentiation. After a week and half of using StemBeads FGF2 I had beautiful plates of undifferentiated stem cells while using half the amount of media. This allowed me to spend more time doing important experiments and spend less money on expensive stem cell media.

Jack Sandoe,
Graduate Student Harvard Stem Cell Institute, 
Kevin Eggan Lab