swiss mouse embryos Search Results


fibroblast feeder cells  (ATCC)
94
ATCC fibroblast feeder cells
Fibroblast Feeder Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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nih/3t3  (ATCC)
99
ATCC nih/3t3
Nih/3t3, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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e15/e16 swiss mouse embryos  (Harlan UK Ltd)
90
Harlan UK Ltd e15/e16 swiss mouse embryos
E15/E16 Swiss Mouse Embryos, supplied by Harlan UK Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cd-1 murine embryos  (Charles River Laboratories)
90
Charles River Laboratories cd-1 murine embryos
Cd 1 Murine Embryos, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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swiss mouse embryos  (Charles River Laboratories)
90
Charles River Laboratories swiss mouse embryos
Swiss Mouse Embryos, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
swiss mouse embryos - by Bioz Stars, 2026-04
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nih swiss mouse embryos  (Harlan Sprague Dawley)
90
Harlan Sprague Dawley nih swiss mouse embryos
Nih Swiss Mouse Embryos, supplied by Harlan Sprague Dawley, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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microglial cultures derived from e13.5 mouse embryos  (Janvier Labs)
90
Janvier Labs microglial cultures derived from e13.5 mouse embryos
<t>Microglial</t> cells were incubated with three different doses of JN403 (100 nM, 1 μM, and 10 μM) for 24 hours, followed by an assessment of cell viability using the MTT-assay. (A) JN403 treatment alone did not elicit cellular toxicity in microglial cells at concentrations up to 1 μM. non-significant (n.s). (B) Microglial cells were pre-treated with 100 nM or 1 μM of JN403 for 24 hours and additionally coincubated for another 24 hours with 1μM αSyn fragment 61-140 on the next day. αSyn induced cytotoxicity in microglial cells. Neither 100 nM nor 1 μM of JN403 treatment changed the cell viability. Data are presented as the mean ± standard error of the mean. Cell viability was measured for multiple independent experiments. **** p < 0.0001, significantly different from the control group.
Microglial Cultures Derived From E13.5 Mouse Embryos, supplied by Janvier Labs, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
microglial cultures derived from e13.5 mouse embryos - by Bioz Stars, 2026-04
90/100 stars
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neocortices of swiss mouse embryos  (Charles River Laboratories)
90
Charles River Laboratories neocortices of swiss mouse embryos
<t>Microglial</t> cells were incubated with three different doses of JN403 (100 nM, 1 μM, and 10 μM) for 24 hours, followed by an assessment of cell viability using the MTT-assay. (A) JN403 treatment alone did not elicit cellular toxicity in microglial cells at concentrations up to 1 μM. non-significant (n.s). (B) Microglial cells were pre-treated with 100 nM or 1 μM of JN403 for 24 hours and additionally coincubated for another 24 hours with 1μM αSyn fragment 61-140 on the next day. αSyn induced cytotoxicity in microglial cells. Neither 100 nM nor 1 μM of JN403 treatment changed the cell viability. Data are presented as the mean ± standard error of the mean. Cell viability was measured for multiple independent experiments. **** p < 0.0001, significantly different from the control group.
Neocortices Of Swiss Mouse Embryos, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/neocortices of swiss mouse embryos/product/Charles River Laboratories
Average 90 stars, based on 1 article reviews
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90/100 stars
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mouse embryos and cell lines swiss webster  (Jackson Laboratory)
90
Jackson Laboratory mouse embryos and cell lines swiss webster
<t>Microglial</t> cells were incubated with three different doses of JN403 (100 nM, 1 μM, and 10 μM) for 24 hours, followed by an assessment of cell viability using the MTT-assay. (A) JN403 treatment alone did not elicit cellular toxicity in microglial cells at concentrations up to 1 μM. non-significant (n.s). (B) Microglial cells were pre-treated with 100 nM or 1 μM of JN403 for 24 hours and additionally coincubated for another 24 hours with 1μM αSyn fragment 61-140 on the next day. αSyn induced cytotoxicity in microglial cells. Neither 100 nM nor 1 μM of JN403 treatment changed the cell viability. Data are presented as the mean ± standard error of the mean. Cell viability was measured for multiple independent experiments. **** p < 0.0001, significantly different from the control group.
Mouse Embryos And Cell Lines Swiss Webster, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
mouse embryos and cell lines swiss webster - by Bioz Stars, 2026-04
90/100 stars
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Image Search Results


Microglial cells were incubated with three different doses of JN403 (100 nM, 1 μM, and 10 μM) for 24 hours, followed by an assessment of cell viability using the MTT-assay. (A) JN403 treatment alone did not elicit cellular toxicity in microglial cells at concentrations up to 1 μM. non-significant (n.s). (B) Microglial cells were pre-treated with 100 nM or 1 μM of JN403 for 24 hours and additionally coincubated for another 24 hours with 1μM αSyn fragment 61-140 on the next day. αSyn induced cytotoxicity in microglial cells. Neither 100 nM nor 1 μM of JN403 treatment changed the cell viability. Data are presented as the mean ± standard error of the mean. Cell viability was measured for multiple independent experiments. **** p < 0.0001, significantly different from the control group.

Journal: bioRxiv

Article Title: JN403, an alpha-7-nicotine-acetylcholine-receptor agonist, reduces alpha-synuclein induced inflammatory parameters of in vitro microglia but fails to attenuate the reduction of TH positive nigral neurons in a focal alpha-synuclein overexpression mouse model of Parkinson’s disease

doi: 10.1101/2020.04.04.996892

Figure Lengend Snippet: Microglial cells were incubated with three different doses of JN403 (100 nM, 1 μM, and 10 μM) for 24 hours, followed by an assessment of cell viability using the MTT-assay. (A) JN403 treatment alone did not elicit cellular toxicity in microglial cells at concentrations up to 1 μM. non-significant (n.s). (B) Microglial cells were pre-treated with 100 nM or 1 μM of JN403 for 24 hours and additionally coincubated for another 24 hours with 1μM αSyn fragment 61-140 on the next day. αSyn induced cytotoxicity in microglial cells. Neither 100 nM nor 1 μM of JN403 treatment changed the cell viability. Data are presented as the mean ± standard error of the mean. Cell viability was measured for multiple independent experiments. **** p < 0.0001, significantly different from the control group.

Article Snippet: Briefly, microglial cultures derived from E13.5 mouse embryos (Janvier Breeding Center, France) were obtained by mild trypsinization as described previously.

Techniques: Incubation, MTT Assay, Control

Inflammatory parameters (A) Nitric Oxide (NO) and (B) TNF-α were measured in JN403 pre-treated microglial cells for a baseline. (A) NO, and (B) TNF-α release increased with 1μM αSyn incubation, but both 100 nM and 1 μM of JN403 co-treatment significantly reduced NO and TNF-α release, * p < 0.05, ** p < 0.01.

Journal: bioRxiv

Article Title: JN403, an alpha-7-nicotine-acetylcholine-receptor agonist, reduces alpha-synuclein induced inflammatory parameters of in vitro microglia but fails to attenuate the reduction of TH positive nigral neurons in a focal alpha-synuclein overexpression mouse model of Parkinson’s disease

doi: 10.1101/2020.04.04.996892

Figure Lengend Snippet: Inflammatory parameters (A) Nitric Oxide (NO) and (B) TNF-α were measured in JN403 pre-treated microglial cells for a baseline. (A) NO, and (B) TNF-α release increased with 1μM αSyn incubation, but both 100 nM and 1 μM of JN403 co-treatment significantly reduced NO and TNF-α release, * p < 0.05, ** p < 0.01.

Article Snippet: Briefly, microglial cultures derived from E13.5 mouse embryos (Janvier Breeding Center, France) were obtained by mild trypsinization as described previously.

Techniques: Incubation

Iba1+ microglial cells were detected and the density analysis showed no differences between the rAAV groups and treatment groups. (A) Representative photomicrographs showing Iba1+ signals per group, TH (green) and Iba1 (magenta). No activated forms of microglia were found. Scale bar 200 μm. (B) The ratio of Iba1+ density of the injected side compared to the non-injected side showed no significant differences between the rAAVs and treatment, n=4, non-significant (n.s).

Journal: bioRxiv

Article Title: JN403, an alpha-7-nicotine-acetylcholine-receptor agonist, reduces alpha-synuclein induced inflammatory parameters of in vitro microglia but fails to attenuate the reduction of TH positive nigral neurons in a focal alpha-synuclein overexpression mouse model of Parkinson’s disease

doi: 10.1101/2020.04.04.996892

Figure Lengend Snippet: Iba1+ microglial cells were detected and the density analysis showed no differences between the rAAV groups and treatment groups. (A) Representative photomicrographs showing Iba1+ signals per group, TH (green) and Iba1 (magenta). No activated forms of microglia were found. Scale bar 200 μm. (B) The ratio of Iba1+ density of the injected side compared to the non-injected side showed no significant differences between the rAAVs and treatment, n=4, non-significant (n.s).

Article Snippet: Briefly, microglial cultures derived from E13.5 mouse embryos (Janvier Breeding Center, France) were obtained by mild trypsinization as described previously.

Techniques: Injection