Examples of 'splenocyte' in a sentence
Meaning of "splenocyte"
splenocyte (noun): A type of white blood cell derived from the spleen, important for immune responses and fighting infections
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- A type of monocyte characteristically found in spleen tissue
How to use "splenocyte" in a sentence
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splenocyte
In some embodiments the cell may be a splenocyte.
A splenocyte is a cell produced in the spleen.
Cytokine levels in lung homogenates are determined as in splenocyte supernatants.
The splenocyte suspensions were then divided into halves.
A particularly preferred immunocyte is a splenocyte.
Splenocyte specific proliferation assays were performed for each group.
Four individual assay chambers were counted per splenocyte preparation.
Values of stimulated splenocyte cultures with those of unstimulated control cultures.
According to other embodiments the human lymphoid cell is a lymph node lymphocyte or a splenocyte.
Splenocyte proliferation assay.
Comparison of the ability of different splenocyte populations to present soluble or particulate antigens.
The mouse spleens were harvested and lymphocytes were isolated from the splenocyte mixture.
Therefore significant reductions in splenocyte counts with all treatments compared to vehicle.
Splenocyte isolation Preparation of spleen cell suspension.
Data gathered from blood and splenocyte samples demonstrated similar results.
See also
Figure 3 shows the effect by the test substance on ex vivo mouse splenocyte activation.
MIMP did not affect splenocyte responses in the absence of mitogens.
Figure 1 shows the effect of various phosphorothioate oligonucleotides on in vitro murine splenocyte proliferation.
Then the supernatant containing the single cell splenocyte suspension was transferred to a fresh tube.
After 14 days the mice were sacrificed and the spleen were removed to obtain splenocyte suspensions.
Each band represents pooled splenocyte extracts from 3 mice.
The syngeneic splenocyte control did not elicit a detectable adaptive immune response ( results not shown ).
Table III shows the data of the splenocyte activation in the mouse.
Murine splenocyte suspensions were prepared from BALB / c mice.
Proliferative recall responses to Collagen II were seen in splenocyte cultures from all experimental groups.
Splenocyte proliferation was measured by the MTT assay and shown as a stimulation index ( SI ).
This is achieved using a conventional splenocyte co-culture system.
Splenocyte responses to PHA preferentially reflect T lymphocyte responses, confirming the responses seen with ConA.
All animals were culled 2 hours later and splenocyte cytokine secretion measured in vitro.
Capacity for induction of lymphokines by Balb / c mouse splenocyte.
In these experiments the splenocyte populations were prepared from non-immunized mice.
Briefly, spleens isolated from BALB / c mice were used to prepare splenocyte suspensions.
Positive control wells received splenocyte suspensions in the absence of the test extracts / compounds.
Figures 8 and 9 demonstrate the effect of NCM treatment in vivo on splenocyte and thymocyte markers.
Since Compound 1 does not alter splenocyte proliferation in vitro, we favor the later explanation.
Cells were harvested at days 2, 4 and 6 following preparation of the splenocyte cultures.
One female Lewis rat served as the splenocyte donor for each group ( experimental condition ).
Figure 3 shows the effect . of different modified HIV-1 rev oligonucleotides on murine splenocyte proliferation.
No proliferation was detected in splenocyte cultures stimulated in vitro with B-glucan of C. albicans.
Splenocyte suspensions were prepared by removing the spleens and placing them into RPMI 1640 medium.
To evaluate lymphocyte lytic activity in mice in vivo, splenocyte isolation and evaluation was performed.
Mouse splenocyte preparation,.
For the mouse cell study, MIR and mouse splenocyte assays were used.
Conventional murine splenocyte assay for immunosuppressive activity . Example 3.
Treatment was incubated with BMDC for 24 hours followed by 4 day co-incubation with WT splenocyte.
A volume of 0.2 ml of the splenocyte suspension was added to replicate test wells.
Figure 2 shows that mouse IFN a / B induced STAT1 phosphorylation in all splenocyte subsets analysed.
A volume of 0.2 ml of the combined splenocyte suspensions was added to triplicate test wells.
Splenocyte effectors were added to obtain effector to target ratio of 5:1 and 1:1 respectively.
That represents OVA-stimulated splenocyte cpm/non-stimulated splenocyte cpm.
