neural maintenance medium Search Results


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Axol Bioscience axol neural maintenance xf medium
Axol Neural Maintenance Xf Medium, supplied by Axol Bioscience, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/neural+maintenance+medium/154367__Implementation_of_High_Throughput_Screening_on_iPS_cells_ascii45_final_ascii46_pdf-11-36-36?v=Axol+Bioscience
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axol neural maintenance xf medium - by Bioz Stars, 2026-07
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Axol Bioscience neural maintenance medium kit
Neural Maintenance Medium Kit, supplied by Axol Bioscience, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/neural+maintenance+medium/pm36310202-122-32-31?v=Axol+Bioscience
Average 93 stars, based on 1 article reviews
neural maintenance medium kit - by Bioz Stars, 2026-07
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90
Lonza neural progenitor maintenance media bullet kit cc-3210
Neural Progenitor Maintenance Media Bullet Kit Cc 3210, supplied by Lonza, 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/product/neural+maintenance+medium/pm20639497-48-6-13?v=Lonza
Average 90 stars, based on 1 article reviews
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Lonza neural progenitor maintenance medium npmm
Neural Progenitor Maintenance Medium Npmm, supplied by Lonza, 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
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XCell Science neural stem cell maintenance medium
In vitro differentiated neurons recapitulate key transcriptional signatures of neurotypes identified from <t>single-cell</t> RNA-sequencing of human ventral midbrain (A) Differentiation of neuronal <t>stem</t> cells (NSCs) into <t>neural</t> progenitor cells (NPCs) and mature neurons (Day 14), followed by 3 additional weeks of culture. Cells were harvested on different day “D” for experiment. (B) Measurement of ApoE and MAP2 mRNA level by quantitative PCR (qPCR) in isogenic control and ApoE−/− cells harvested on different day. Data are presented as mean ± S.D. (triplicate qPCR reactions, 2-tailed t -tests). (C) Representative immunoblots and MAP2 quantification of cells harvested on different days. Lysates were probed with MAP2, actin and ApoE antibodies. The level of MAP2 was normalized to actin and quantified with reference to Day 14 control neurons. Data presented as mean ± S.E.M (∗∗p < 0.005, n = 5. 2-tailed paired t -test). (D) Representative immmunofluorescence images of Day 14 neurons stained with MAP2 and DAPI. The scale bars represent 150 μm. (E) RNA-seq volcano plots of differentially expressed genes between NSC and Day 14 neurons as determined by DESeq2 with Log 2 (2-fold change) threshold and adjusted p-value <0.05. (F) Top 10 enriched gene ontology terms (BP: Biological Process) for genes highly expressed in either control or ApoE−/− neurons (left) and NSC (right). (G) Ranked enrichment analysis of gene expression signatures in control and ApoE−/− cells (Negative: NSC; Positive: Neurons) by directional fgsea statistical enrichment test using cell type signature gene sets. “h” indicates human; GABA: GABAergic neurons; CTX: cerebral cortex; DA: dopaminergic neurons; SERT: serotonergic; NB: neuroblast; NbML: mediolateral neuroblasts; OMTN: oculomotor and trochlear nucleus; RN: red nucleus; OPC: oligodendrocyte precursor cells; PROG: Progenitor; FPL: lateral floorplate; BP: basal plate; FPM: medial floorplate; ENDO: endothelial cells; PFC: prefrontal cortex.
Neural Stem Cell Maintenance Medium, supplied by XCell Science, 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/product/neural+maintenance+medium/pmc10909902-35-0-6?v=XCell+Science
Average 90 stars, based on 1 article reviews
neural stem cell maintenance medium - by Bioz Stars, 2026-07
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BioWhittaker Molecular Applications neural progenitor maintenance medium bullet kit
In vitro differentiated neurons recapitulate key transcriptional signatures of neurotypes identified from <t>single-cell</t> RNA-sequencing of human ventral midbrain (A) Differentiation of neuronal <t>stem</t> cells (NSCs) into <t>neural</t> progenitor cells (NPCs) and mature neurons (Day 14), followed by 3 additional weeks of culture. Cells were harvested on different day “D” for experiment. (B) Measurement of ApoE and MAP2 mRNA level by quantitative PCR (qPCR) in isogenic control and ApoE−/− cells harvested on different day. Data are presented as mean ± S.D. (triplicate qPCR reactions, 2-tailed t -tests). (C) Representative immunoblots and MAP2 quantification of cells harvested on different days. Lysates were probed with MAP2, actin and ApoE antibodies. The level of MAP2 was normalized to actin and quantified with reference to Day 14 control neurons. Data presented as mean ± S.E.M (∗∗p < 0.005, n = 5. 2-tailed paired t -test). (D) Representative immmunofluorescence images of Day 14 neurons stained with MAP2 and DAPI. The scale bars represent 150 μm. (E) RNA-seq volcano plots of differentially expressed genes between NSC and Day 14 neurons as determined by DESeq2 with Log 2 (2-fold change) threshold and adjusted p-value <0.05. (F) Top 10 enriched gene ontology terms (BP: Biological Process) for genes highly expressed in either control or ApoE−/− neurons (left) and NSC (right). (G) Ranked enrichment analysis of gene expression signatures in control and ApoE−/− cells (Negative: NSC; Positive: Neurons) by directional fgsea statistical enrichment test using cell type signature gene sets. “h” indicates human; GABA: GABAergic neurons; CTX: cerebral cortex; DA: dopaminergic neurons; SERT: serotonergic; NB: neuroblast; NbML: mediolateral neuroblasts; OMTN: oculomotor and trochlear nucleus; RN: red nucleus; OPC: oligodendrocyte precursor cells; PROG: Progenitor; FPL: lateral floorplate; BP: basal plate; FPM: medial floorplate; ENDO: endothelial cells; PFC: prefrontal cortex.
Neural Progenitor Maintenance Medium Bullet Kit, supplied by BioWhittaker Molecular Applications, 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/product/neural+maintenance+medium/us07807458-1036-12-23?v=BioWhittaker+Molecular+Applications
Average 90 stars, based on 1 article reviews
neural progenitor maintenance medium bullet kit - by Bioz Stars, 2026-07
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90
DV Biologics neural maintenance medium n-gro
In vitro differentiated neurons recapitulate key transcriptional signatures of neurotypes identified from <t>single-cell</t> RNA-sequencing of human ventral midbrain (A) Differentiation of neuronal <t>stem</t> cells (NSCs) into <t>neural</t> progenitor cells (NPCs) and mature neurons (Day 14), followed by 3 additional weeks of culture. Cells were harvested on different day “D” for experiment. (B) Measurement of ApoE and MAP2 mRNA level by quantitative PCR (qPCR) in isogenic control and ApoE−/− cells harvested on different day. Data are presented as mean ± S.D. (triplicate qPCR reactions, 2-tailed t -tests). (C) Representative immunoblots and MAP2 quantification of cells harvested on different days. Lysates were probed with MAP2, actin and ApoE antibodies. The level of MAP2 was normalized to actin and quantified with reference to Day 14 control neurons. Data presented as mean ± S.E.M (∗∗p < 0.005, n = 5. 2-tailed paired t -test). (D) Representative immmunofluorescence images of Day 14 neurons stained with MAP2 and DAPI. The scale bars represent 150 μm. (E) RNA-seq volcano plots of differentially expressed genes between NSC and Day 14 neurons as determined by DESeq2 with Log 2 (2-fold change) threshold and adjusted p-value <0.05. (F) Top 10 enriched gene ontology terms (BP: Biological Process) for genes highly expressed in either control or ApoE−/− neurons (left) and NSC (right). (G) Ranked enrichment analysis of gene expression signatures in control and ApoE−/− cells (Negative: NSC; Positive: Neurons) by directional fgsea statistical enrichment test using cell type signature gene sets. “h” indicates human; GABA: GABAergic neurons; CTX: cerebral cortex; DA: dopaminergic neurons; SERT: serotonergic; NB: neuroblast; NbML: mediolateral neuroblasts; OMTN: oculomotor and trochlear nucleus; RN: red nucleus; OPC: oligodendrocyte precursor cells; PROG: Progenitor; FPL: lateral floorplate; BP: basal plate; FPM: medial floorplate; ENDO: endothelial cells; PFC: prefrontal cortex.
Neural Maintenance Medium N Gro, supplied by DV Biologics, 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/product/neural+maintenance+medium/pm28210976-70-19-22?v=DV+Biologics
Average 90 stars, based on 1 article reviews
neural maintenance medium n-gro - by Bioz Stars, 2026-07
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N/A
Culture system containing PBMTM Neural Progenitor Basal Medium (CC-3210), NPMMTM Maintenance Media SingleQuotsTM (CC-4241) and Neural Progenitor Supplement SingleQuotsTM (CC-4242) required for growth and differentiation of neural progenitor cells
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In vitro differentiated neurons recapitulate key transcriptional signatures of neurotypes identified from single-cell RNA-sequencing of human ventral midbrain (A) Differentiation of neuronal stem cells (NSCs) into neural progenitor cells (NPCs) and mature neurons (Day 14), followed by 3 additional weeks of culture. Cells were harvested on different day “D” for experiment. (B) Measurement of ApoE and MAP2 mRNA level by quantitative PCR (qPCR) in isogenic control and ApoE−/− cells harvested on different day. Data are presented as mean ± S.D. (triplicate qPCR reactions, 2-tailed t -tests). (C) Representative immunoblots and MAP2 quantification of cells harvested on different days. Lysates were probed with MAP2, actin and ApoE antibodies. The level of MAP2 was normalized to actin and quantified with reference to Day 14 control neurons. Data presented as mean ± S.E.M (∗∗p < 0.005, n = 5. 2-tailed paired t -test). (D) Representative immmunofluorescence images of Day 14 neurons stained with MAP2 and DAPI. The scale bars represent 150 μm. (E) RNA-seq volcano plots of differentially expressed genes between NSC and Day 14 neurons as determined by DESeq2 with Log 2 (2-fold change) threshold and adjusted p-value <0.05. (F) Top 10 enriched gene ontology terms (BP: Biological Process) for genes highly expressed in either control or ApoE−/− neurons (left) and NSC (right). (G) Ranked enrichment analysis of gene expression signatures in control and ApoE−/− cells (Negative: NSC; Positive: Neurons) by directional fgsea statistical enrichment test using cell type signature gene sets. “h” indicates human; GABA: GABAergic neurons; CTX: cerebral cortex; DA: dopaminergic neurons; SERT: serotonergic; NB: neuroblast; NbML: mediolateral neuroblasts; OMTN: oculomotor and trochlear nucleus; RN: red nucleus; OPC: oligodendrocyte precursor cells; PROG: Progenitor; FPL: lateral floorplate; BP: basal plate; FPM: medial floorplate; ENDO: endothelial cells; PFC: prefrontal cortex.

Journal: iScience

Article Title: ApoE maintains neuronal integrity via microRNA and H3K27me3-mediated repression

doi: 10.1016/j.isci.2024.109231

Figure Lengend Snippet: In vitro differentiated neurons recapitulate key transcriptional signatures of neurotypes identified from single-cell RNA-sequencing of human ventral midbrain (A) Differentiation of neuronal stem cells (NSCs) into neural progenitor cells (NPCs) and mature neurons (Day 14), followed by 3 additional weeks of culture. Cells were harvested on different day “D” for experiment. (B) Measurement of ApoE and MAP2 mRNA level by quantitative PCR (qPCR) in isogenic control and ApoE−/− cells harvested on different day. Data are presented as mean ± S.D. (triplicate qPCR reactions, 2-tailed t -tests). (C) Representative immunoblots and MAP2 quantification of cells harvested on different days. Lysates were probed with MAP2, actin and ApoE antibodies. The level of MAP2 was normalized to actin and quantified with reference to Day 14 control neurons. Data presented as mean ± S.E.M (∗∗p < 0.005, n = 5. 2-tailed paired t -test). (D) Representative immmunofluorescence images of Day 14 neurons stained with MAP2 and DAPI. The scale bars represent 150 μm. (E) RNA-seq volcano plots of differentially expressed genes between NSC and Day 14 neurons as determined by DESeq2 with Log 2 (2-fold change) threshold and adjusted p-value <0.05. (F) Top 10 enriched gene ontology terms (BP: Biological Process) for genes highly expressed in either control or ApoE−/− neurons (left) and NSC (right). (G) Ranked enrichment analysis of gene expression signatures in control and ApoE−/− cells (Negative: NSC; Positive: Neurons) by directional fgsea statistical enrichment test using cell type signature gene sets. “h” indicates human; GABA: GABAergic neurons; CTX: cerebral cortex; DA: dopaminergic neurons; SERT: serotonergic; NB: neuroblast; NbML: mediolateral neuroblasts; OMTN: oculomotor and trochlear nucleus; RN: red nucleus; OPC: oligodendrocyte precursor cells; PROG: Progenitor; FPL: lateral floorplate; BP: basal plate; FPM: medial floorplate; ENDO: endothelial cells; PFC: prefrontal cortex.

Article Snippet: Neural stem cell maintenance medium , XCell Science Inc. , Cat#SM-001-BM100.

Techniques: In Vitro, RNA Sequencing, Real-time Polymerase Chain Reaction, Control, Western Blot, Staining, Gene Expression

Journal: iScience

Article Title: ApoE maintains neuronal integrity via microRNA and H3K27me3-mediated repression

doi: 10.1016/j.isci.2024.109231

Figure Lengend Snippet:

Article Snippet: Neural stem cell maintenance medium , XCell Science Inc. , Cat#SM-001-BM100.

Techniques: Recombinant, Transfection, Reverse Transcription, Imaging, Expressing, Control, Knock-Out, Sequencing, Negative Control, Plasmid Preparation, Software, Functional Assay