Gibco™ CELLstart™ Substrate

In addition to the StemPRO hESC SFM kit, you will also need the following to make a complete medium: full length recombinant human FGF (catalog # PHG0261) and 2-Mercaptoethanol (catalog # 21985-023).

The StemPro hESC SFM kit (Cat. No. A1000701) contains: - 500 mL DMEM/F-12 with GlutaMax (Cat. No. 10565-018)
- 10 mL StemPro hESC SFM Supplement 50X (Cat. No. A10006-01)
- 40 mL Bovine Serum Albumin 25% (BSA Solution) (Cat. No. A10008-01)
Note that the StemPRO hESC Supplement and BSA solution cannot be ordered individually.

CELLstart substrate has also been tested with the following hESC: RCM-1, H9, BG01v, I3, I6. CELLstart substrate has been tested with the following other primary and stem cells: human foreskin fibroblasts, mouse fibroblasts, H-9 derived NSCs and bone marrow-derived MSCs.

CELLstart substrate has been tested with Stempro hESC SFM, Stempro MSC SFM, Stempro NSC SFM, Essential 8, and Mouse embryonic fibroblast (MEF) -conditioned medium generated using Knockout Serum Replacement.

Yes, it's normal to have changes in morphology when switching to a new cell culture system. Even with differences in morphology, pluripotency is still retained.

In general, yes. However, this may be dependent on the hESC line and the split ratio (seeding density) may need to be optimized to achieve the desired proliferation rate.

We recommend using dishes that are coated less than 48 hours before use. Depending on the sensitivity of your cells, you may be able to coat plates and store them for up to two weeks before use. If the coated plates are stored, they should be stored at 2C-8C, with parafilm tightly sealing the plates. Bring the plates to room temperature and aspirate liquid before use.

Yes, the cells can be plated from a single cell suspension. Ensure that the medium is supplemented with ROCK inhibitor to maintain pluripotency of hESCs.

We recommend a 1:50 dilution for hESC applications. However, you may optimize this dilution based on your hESC line if you desire. For dilution instructions for MSC and NSC applications, see the product manual for StemPro MSC SFM or StemPRO NSC SFM.

Yes, the gelling is a normal characteristic of CELLstart substrate, and we have provided sufficient volume in the vial to accommodate this gelling. The gelling does not have an impact on performance of the remaining product. Use only the liquid, allowing the gelled material to remain in the vial.

Yes, enzymes can be used. We recommended TrypLE Select. We do not recommend collagenase or dispase due to lot variability of these products, animal origin composition, and the damage they can do to the cells.

Growth factors used for MSC maintenance and self-renewal: LIF, FGF-basic, EGF, HGF, PDGF, and Wnt3.

Growth factors or cytokines for MSC differentiation: BMP-2and TGF-β1.

(Arthritis Res Ther 9:204 (2007)

View our Gibco™ MSC research products.

MSCs may be cultured in either serum-containing medium or serum-free medium. The standard culturing conditions are DMEM, low glucose with 10% FBS. MSCs can also be grown in reduced-serum (2%) Gibco MesenPRO RS Medium (Cat. No. 12746-012), or in serum-free Gibco StemPro MSC SFM XenoFree Medium (Cat. No. A10675) and Gibco StemPro MSC SFM (Cat. No. A10332). In general, MSCs grow better under hypoxic conditions (2% O2).

Human MSCs can be identified by flow cytometry, typically displaying CD73+, CD90+, CD105+, CD11b-, and CD45- marker characteristics (Blood 109:4245 (2007)). Human MSC expresses Oct4, Sox2, and Rex-1; these may be verified using RT-PCR (Arthritis Res Ther 9:204 (2007)).

Mesenchymal stem cells (MSCs) are multipotent cells isolated primarily from bone marrow or fat tissues that exhibit the ability to differentiate into bone, cartilage, and fat cells. Under normal cell culture conditions, MSCs isolated from bone marrow are spindle shaped with the unique ability to adhere to uncoated plastic culture dishes (Arthritis Res Ther 9:204 (2007)).

Human ES cells are generally characterized by their typical morphology (they grow as tightly packed clusters of small cells with high ratio of nucleus to cytoplasm); surface marker expression; RT-PCR detection of stem cell-specific gene expression (such as Oct3/4, Sox2, and Nanog); alkaline phosphatase staining, and telomerase activity assay. The most commonly used ES specific surface markers include stage-specific embryonic antigens SSEA-3 and SSEA-4 for human ES cells. Other ES-specific surface antigens also include TRA-1-60 and TRA-1-81. (Science 282:1145 (1998).

Human ES cells are derived from human blastocyst inner cell masses, isolated by immunosurgery with rabbit antiserum to BeWO cells (a human trophoblast cell line) (Science 282:1145 (1998)).

Embryonic stem (ES) cells are derived from the early mammalian embryo and are capable of unlimited, undifferentiated proliferation in vitro while maintaining their potential to differentiate into a wide of range of adult tissues including germ cells. The pluripotency of the ES cells is normally demonstrated in vitro by inducing ES cells to differentiate into embryoid bodies and checking lineage-specific markers for differentiated cells in three body layers (endo, meso, and ectoderm), or injecting them into immunodeficient mice and determining the cell types produced in the teratomas.

Gibco Geltrex Matrix and collagen (rat tail and bovine) can be used as either a coating solution or a 3D gel matrix. CELLstart Substrate was developed to be used as a xeno-free coating matrix for only ESC applications (as a substitute for Gibco Geltrex Matrix or Matrigel Matrix, which are of animal origin). AlgiMatrix Matrix is a 3D scaffold-type matrix that does not support cell attachment but does provide a good environment for growing spheroids that can be easily harvested for downstream applications.