Mouse Methylcellulose Complete Media Without Epo
R&D Systems, part of Bio-Techne | Catalog # HSC008
Key Product Details
Assay Procedure
Refer to the product datasheet for complete product details.
Briefly, Mouse Methylcellulose Complete Media Without Epo is used in the Colony Forming Cell Assay using the following procedure:
- Prepare mouse bone marrow cells
- Add cells to Mouse Methylcellulose Complete Media Without Epo
- Plate and incubate cells
- Identify and count colonies
Reagent supplied in the Mouse Methylcellulose Complete Media Without Epo (Catalog # HSC008):
- 100 mL of Mouse Methylcellulose Complete Media Without Epo.
Contents | Concentration (when diluted to a final volume of 100 mL) |
Methylcellulose (1500 cps) in Iscove's Modified Dulbecco's Medium | 1.4% |
Fetal Bovine Serum | 15% |
Bovine Serum Albumin | 2% |
L-Glutamine | 2 mM |
2-Mercaptoethanol | 5 x 10-5 M |
Recombinant Human Insulin | 10 µg/mL |
Human Transferrin | 200 µg/mL |
Recombinant Human SCF | 50 ng/mL |
Recombinant Human IL-3 | 10 ng/mL |
Recombinant Human IL-6 | 10 ng/mL |
Reagents
- Cells derived from mouse bone marrow, spleen, peripheral blood, or fetal liver. Mice are routinely used between 6 - 12 weeks.
- Iscove's Modified Dulbecco's Media (IMDM)
- Fetal Bovine Serum
- IMDM/2% Fetal Bovine Serum
- (Optional) Flow Cytometry Mouse Lyse Buffer (Catalog # FC003)
Materials
- 100 mm culture plates
- 35 mm culture plates
- 15 mL centrifuge tubes
- 10 mL syringes
- 3 mL syringes
- 5 mL vials
- 16 gauge 1½ inch needle
- 14 gauge laboratory pipetting needle
- Serological pipettes
- Pipettes and pipette tips
Equipment
- 37 °C and CO2 humidified incubator
- Centrifuge
- Vortex mixer
- Hemocytometer
- Inverted Microscope
Pass a suspension of mouse bone marrow cells through a 70 µm nylon strainer to remove clumps and debris.
Remove red blood cells if necessary.
Wash the cells with IMDM/2% FBS by centrifugation at 300 x g for 8 minutes and pool the cells.

Remove the supernatant.
Resuspend the cells in 10 mL of IMDM/2% FBS

Thaw aliquots of Mouse Methylcellulose Complete Media Without EPO at room temperature for approximately 30 minutes.

Perform a cell count.

Transfer the appropriate volume of cells (plus a slight excess) into a new 15 mL centrifuge tube.
Centrifuge at 300 x g for 8 minutes.

Remove the supernatant.
Resuspend the cells in IMDM/2% FBS to the desired stock cell number to generate a 10X stock concentration.

Combine the appropriate volume of 10X cell stock with the desired cell culture supplements/cytokines, and Mouse Mouse Methylcellulose Complete Media Without EPO. The final Methylcellulose concentration should be 1.27%.

Vortex the samples vigorously.
Wait approximately 20 minutes to allow air bubbles to escape.
Add 1.1 mL of the cell mixture to a 35 mm culture plate using a 3 mL syringe and a 16 gauge needle.
Spread the media evenly.

Place two 35 mm plates into a 10 cm plate.
Add one uncovered 35 mm plate that contains 3-4 mL of sterile water.
Cover the 10 cm plate and place it in a 37 °C and 5% CO2 incubator.
Incubate the cells for 8-12 days.

Use an inverted microscope and a scoring grid to identify and count individual colonies.

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