Examples of 'differentiation medium' in a sentence

Meaning of "differentiation medium"

differentiation medium - In biology, this term refers to a substance used to distinguish between different types of organisms or cells based on specific characteristics or behaviors

How to use "differentiation medium" in a sentence

Basic
Advanced
differentiation medium
Cells in differentiation medium containing no additive were used as control.
Cells were then seeded into fresh differentiation medium.
Basal differentiation medium.
These effects are similar to those of the complete differentiation medium.
Liver cell differentiation medium.
The differentiation capacity of these cells was tested by culturing in a differentiation medium.
Keratinocyte differentiation medium.
The cells can also differentiate in vitro by culturing the cells in differentiation medium.
The differentiation medium isperiodically or continuously replaced with fresh differentiation medium from the reservoir system.
Typically this is achieved by replacing the culture medium with expansion and differentiation medium.
Differentiation medium Medium used for culturing animal cells can be prepared as basal medium.
BMSC were maintained in a conventional osteoblastic differentiation medium.
A liquid chondrogenic differentiation medium comprising,.
The culture was transferred to MB medium and subsequently to a differentiation medium.
The differentiation medium has the following essential composition,.

See also

USSCs were cultured in a chondrogenic differentiation medium.
The differentiation medium was substituted by half with a fresh one, twice a week.
USSCs were grown under sedimentation culture in a chondrogenic differentiation medium.
The medium was changed with new differentiation medium 4 hours post transfection.
Osteogenic differentiation was induced by replacing the medium with Osteogenic Differentiation medium.
According to a second embodiment, the differentiation medium contains human serum.
Differentiation medium was changed every three days and gels were cultured for 10 days.
In some embodiments, the culture medium is a differentiation medium.
The osteoblast differentiation medium was replaced with fresh medium every 3 days for 3 weeks.
On day 2 no additional insulin was added in the differentiation medium.
Culture in adipogenic differentiation medium was as described in Example 6.
After three weeks, the culture was transferred to selective differentiation medium.
After differentiation medium reached room temperature, about 20 mL was poured into a small beaker.
In some embodiments, gastrin can be excluded from this differentiation medium.
Differentiation medium was added, and medium was changed every 3 days for a total of 12 days.
Once the cells have reached confluence, the medium is replaced by a differentiation medium.
The medium was replaced with new differentiation medium every 3 days to induce differentiation for 3-4 weeks.
To induce differentiation of the undifferentiated adipocytes, the cells were then incubated in a differentiation medium.
Next, the cells are put in a differentiation medium for 5 days.
Retinoic acid ( RA ) and ascorbic acid also can be included in a neurogenic differentiation medium.
The liquid chondrogenic differentiation medium according to claim 1, wherein said low-molecular-weight sulfated polysaccharide,.
Once confluent, the cell media formulation is changed to differentiation medium to induce cell differentiation.
Typically, the differentiation medium does not contain a Wnt agonist, R-spondin or Nicotinamide.
Hence, as an embodiment the present invention, providing an autoHS differentiation medium overcomes these problems.
In one embodiment, the differentiation medium comprises EGF, a TGF-beta inhibitor, FGF and a Notch inhibitor.
This alternative second culture medium is useful as a differentiation medium ( DM ).
The cells are then maintained in a differentiation medium for 10 days.
Three days after, IBMX and dexamethasone were withdrawn from the differentiation medium.
The morphology of the CD90 - cells grown in differentiation medium is typically hepatic.
This medium including the growth factors will be referred to as endothelial differentiation medium ( EDM ).
Differentiation was induced at day 7, by adding NSA-A differentiation medium ( StemCell Technologies ) for 21 days.
The cells were grown on sterile 24-well plates with 600 µL of differentiation medium per well.
After one week, the medium is replaced with cartilage differentiation medium supplemented with 10ng/mL Bmp2.

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