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The cells responsible for interacting with stem cells include macrophages, fat cells, reticulum cells, endothelial cells and fibroblasts. Together these constitute the Hematopoietic Microenvironment. Without a fully functional in vivo hematopoietic microenvironment, stem cell will not grow. To determine the presence and whether the MSC will possess the functional ability to proliferate and produce fibroblasts that can help form the hematopoietic microenvironment, two assays are available, namely the CFU-F assay and LUMENESC™-96 QC. The following table shos the differences between these two assays and the advantages of LUMENESC™-96 QC over the CFU-F assay.
| | CFU-F | LUMENESC™-96 QC |
| Assay detects: | Fibroblasts | Fibroblasts |
| Type of assay: | Differentiation | Proliferation |
| Type of culture: | Suspension | Suspension |
| Cell growth: | Expansion | Expansion |
| Parameter measured: | Colony number | Intracellular ATP |
| Type of readout: | Manual | Instrument-based |
| Readout: | Stained colonies | Bioluminescence |
| Subjectivity | Subjective | Non-subjective |
| Standardization: | No | External ATP with high and low controls |
| Format: | 60mm-100mm Petri dishes | 96-well plate |
| Volume of assay: | Several mls | 100µl |
| Number of replicates: | 1-2 | Unlimited |
| Incubation time: | 14-21 days | 10 days |
| Processing time/ reading time: | None / 10min / plate | 20 min / <5 min / plate |
| Training: | > 14 days | 2 days |
| Proficiency testing potential: | None | Yes |