seeding neuronal media Search Results


brainphys neuronal medium  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc brainphys neuronal medium

Brainphys Neuronal Medium, supplied by STEMCELL Technologies Inc, 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/brainphys neuronal medium/product/STEMCELL Technologies Inc
Average 90 stars, based on 1 article reviews
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neuronal media (neurobasal medium-a  (Thermo Fisher)
90
Thermo Fisher neuronal media (neurobasal medium-a

Neuronal Media (Neurobasal Medium A, supplied by Thermo Fisher, 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/neuronal media (neurobasal medium-a/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
neuronal media (neurobasal medium-a - by Bioz Stars, 2026-04
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microfluidic culture device standard neuron device, cat# snd450  (Xona Microfluidics)
90
Xona Microfluidics microfluidic culture device standard neuron device, cat# snd450
A histogram (A) shows particle sizes of MSC-exosomes analyzed by the qNano system. Western blot analysis (B) shows the proteins of Alix and Hsp70 in MSC-exosomes (Exo) and supernatants (Sup). The schematic of a <t>microfluidic</t> culture device and a representative immunofluorescent image (C) show the pNFH+ cortical neurons and axons (green) in the cell body compartment (soma) and pNFH+ axons (green) in the axonal compartment (axon). The compartments are connected by 450 μm long microgrooves (C, microgrooves). DAPI labeled nuclei of cortical neurons (blue) were only present in the cell body compartment (C, soma). Panels D and E show representative images of pNFH+ axons in the axonal compartment (D, green) and quantitative data of the average axonal length (E) from the control (Ctl) and MSC-exosome (Exo) groups when the exosomes were applied into the soma compartment for 24 and 48h. * p<0.001 vs control. Panels F and G show representative time-lapse microscopic images of the growth cone extension (F) and quantitative data of growth cone elongation (G) in the axonal compartment during 60 min from the control (Ctl) and MSC-exosome (Exo) groups. Yellow and red arrows in panel F indicate starting (0 min) and ending (60 min) points, respectively. The representative time-lapse microscopic images (F) were acquired from 24h after soma application of the exosomes, whereas quantitative data (G) were acquired for 24 and 48h after exosome application. *p<0.05 vs control. Sample size in G represents the number of the growth cone from every independent experiment.
Microfluidic Culture Device Standard Neuron Device, Cat# Snd450, supplied by Xona Microfluidics, 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/microfluidic culture device standard neuron device, cat# snd450/product/Xona Microfluidics
Average 90 stars, based on 1 article reviews
microfluidic culture device standard neuron device, cat# snd450 - by Bioz Stars, 2026-04
90/100 stars
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seeding neuronal media  (NeuCyte Inc)
90
NeuCyte Inc seeding neuronal media
A histogram (A) shows particle sizes of MSC-exosomes analyzed by the qNano system. Western blot analysis (B) shows the proteins of Alix and Hsp70 in MSC-exosomes (Exo) and supernatants (Sup). The schematic of a <t>microfluidic</t> culture device and a representative immunofluorescent image (C) show the pNFH+ cortical neurons and axons (green) in the cell body compartment (soma) and pNFH+ axons (green) in the axonal compartment (axon). The compartments are connected by 450 μm long microgrooves (C, microgrooves). DAPI labeled nuclei of cortical neurons (blue) were only present in the cell body compartment (C, soma). Panels D and E show representative images of pNFH+ axons in the axonal compartment (D, green) and quantitative data of the average axonal length (E) from the control (Ctl) and MSC-exosome (Exo) groups when the exosomes were applied into the soma compartment for 24 and 48h. * p<0.001 vs control. Panels F and G show representative time-lapse microscopic images of the growth cone extension (F) and quantitative data of growth cone elongation (G) in the axonal compartment during 60 min from the control (Ctl) and MSC-exosome (Exo) groups. Yellow and red arrows in panel F indicate starting (0 min) and ending (60 min) points, respectively. The representative time-lapse microscopic images (F) were acquired from 24h after soma application of the exosomes, whereas quantitative data (G) were acquired for 24 and 48h after exosome application. *p<0.05 vs control. Sample size in G represents the number of the growth cone from every independent experiment.
Seeding Neuronal Media, supplied by NeuCyte Inc, 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/seeding neuronal media/product/NeuCyte Inc
Average 90 stars, based on 1 article reviews
seeding neuronal media - by Bioz Stars, 2026-04
90/100 stars
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cytosine-β-d arabinofuranoside  (Millipore)
90
Millipore cytosine-β-d arabinofuranoside
A histogram (A) shows particle sizes of MSC-exosomes analyzed by the qNano system. Western blot analysis (B) shows the proteins of Alix and Hsp70 in MSC-exosomes (Exo) and supernatants (Sup). The schematic of a <t>microfluidic</t> culture device and a representative immunofluorescent image (C) show the pNFH+ cortical neurons and axons (green) in the cell body compartment (soma) and pNFH+ axons (green) in the axonal compartment (axon). The compartments are connected by 450 μm long microgrooves (C, microgrooves). DAPI labeled nuclei of cortical neurons (blue) were only present in the cell body compartment (C, soma). Panels D and E show representative images of pNFH+ axons in the axonal compartment (D, green) and quantitative data of the average axonal length (E) from the control (Ctl) and MSC-exosome (Exo) groups when the exosomes were applied into the soma compartment for 24 and 48h. * p<0.001 vs control. Panels F and G show representative time-lapse microscopic images of the growth cone extension (F) and quantitative data of growth cone elongation (G) in the axonal compartment during 60 min from the control (Ctl) and MSC-exosome (Exo) groups. Yellow and red arrows in panel F indicate starting (0 min) and ending (60 min) points, respectively. The representative time-lapse microscopic images (F) were acquired from 24h after soma application of the exosomes, whereas quantitative data (G) were acquired for 24 and 48h after exosome application. *p<0.05 vs control. Sample size in G represents the number of the growth cone from every independent experiment.
Cytosine β D Arabinofuranoside, supplied by Millipore, 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/cytosine-β-d arabinofuranoside/product/Millipore
Average 90 stars, based on 1 article reviews
cytosine-β-d arabinofuranoside - by Bioz Stars, 2026-04
90/100 stars
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amaxa nucleofector device  (Lonza)
90
Lonza amaxa nucleofector device
A histogram (A) shows particle sizes of MSC-exosomes analyzed by the qNano system. Western blot analysis (B) shows the proteins of Alix and Hsp70 in MSC-exosomes (Exo) and supernatants (Sup). The schematic of a <t>microfluidic</t> culture device and a representative immunofluorescent image (C) show the pNFH+ cortical neurons and axons (green) in the cell body compartment (soma) and pNFH+ axons (green) in the axonal compartment (axon). The compartments are connected by 450 μm long microgrooves (C, microgrooves). DAPI labeled nuclei of cortical neurons (blue) were only present in the cell body compartment (C, soma). Panels D and E show representative images of pNFH+ axons in the axonal compartment (D, green) and quantitative data of the average axonal length (E) from the control (Ctl) and MSC-exosome (Exo) groups when the exosomes were applied into the soma compartment for 24 and 48h. * p<0.001 vs control. Panels F and G show representative time-lapse microscopic images of the growth cone extension (F) and quantitative data of growth cone elongation (G) in the axonal compartment during 60 min from the control (Ctl) and MSC-exosome (Exo) groups. Yellow and red arrows in panel F indicate starting (0 min) and ending (60 min) points, respectively. The representative time-lapse microscopic images (F) were acquired from 24h after soma application of the exosomes, whereas quantitative data (G) were acquired for 24 and 48h after exosome application. *p<0.05 vs control. Sample size in G represents the number of the growth cone from every independent experiment.
Amaxa Nucleofector Device, 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/result/amaxa nucleofector device/product/Lonza
Average 90 stars, based on 1 article reviews
amaxa nucleofector device - by Bioz Stars, 2026-04
90/100 stars
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neural progenitor cell basal medium  (Lonza)
90
Lonza neural progenitor cell basal medium
A histogram (A) shows particle sizes of MSC-exosomes analyzed by the qNano system. Western blot analysis (B) shows the proteins of Alix and Hsp70 in MSC-exosomes (Exo) and supernatants (Sup). The schematic of a <t>microfluidic</t> culture device and a representative immunofluorescent image (C) show the pNFH+ cortical neurons and axons (green) in the cell body compartment (soma) and pNFH+ axons (green) in the axonal compartment (axon). The compartments are connected by 450 μm long microgrooves (C, microgrooves). DAPI labeled nuclei of cortical neurons (blue) were only present in the cell body compartment (C, soma). Panels D and E show representative images of pNFH+ axons in the axonal compartment (D, green) and quantitative data of the average axonal length (E) from the control (Ctl) and MSC-exosome (Exo) groups when the exosomes were applied into the soma compartment for 24 and 48h. * p<0.001 vs control. Panels F and G show representative time-lapse microscopic images of the growth cone extension (F) and quantitative data of growth cone elongation (G) in the axonal compartment during 60 min from the control (Ctl) and MSC-exosome (Exo) groups. Yellow and red arrows in panel F indicate starting (0 min) and ending (60 min) points, respectively. The representative time-lapse microscopic images (F) were acquired from 24h after soma application of the exosomes, whereas quantitative data (G) were acquired for 24 and 48h after exosome application. *p<0.05 vs control. Sample size in G represents the number of the growth cone from every independent experiment.
Neural Progenitor Cell Basal Medium, 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/result/neural progenitor cell basal medium/product/Lonza
Average 90 stars, based on 1 article reviews
neural progenitor cell basal medium - by Bioz Stars, 2026-04
90/100 stars
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Image Search Results


Journal: Cell

Article Title: RNA Granules Hitchhike on Lysosomes for Long-Distance Transport, Using Annexin A11 as a Molecular Tether

doi: 10.1016/j.cell.2019.08.050

Figure Lengend Snippet:

Article Snippet: Cells were seeded and maintained in Cortical Neuron Culture Media, composed of BrainPhys Neuronal Medium (STEMCELL Technologies), B-27 supplement (ThermoFisher Scientific), brain-derived neurotrophic factor (10 ng/ml), neurotrophin-3 (10 ng/ml), and mouse laminin (1 μg/ml).

Techniques: Recombinant, Transgenic Assay, shRNA, Sequencing, Modification, Software

A histogram (A) shows particle sizes of MSC-exosomes analyzed by the qNano system. Western blot analysis (B) shows the proteins of Alix and Hsp70 in MSC-exosomes (Exo) and supernatants (Sup). The schematic of a microfluidic culture device and a representative immunofluorescent image (C) show the pNFH+ cortical neurons and axons (green) in the cell body compartment (soma) and pNFH+ axons (green) in the axonal compartment (axon). The compartments are connected by 450 μm long microgrooves (C, microgrooves). DAPI labeled nuclei of cortical neurons (blue) were only present in the cell body compartment (C, soma). Panels D and E show representative images of pNFH+ axons in the axonal compartment (D, green) and quantitative data of the average axonal length (E) from the control (Ctl) and MSC-exosome (Exo) groups when the exosomes were applied into the soma compartment for 24 and 48h. * p<0.001 vs control. Panels F and G show representative time-lapse microscopic images of the growth cone extension (F) and quantitative data of growth cone elongation (G) in the axonal compartment during 60 min from the control (Ctl) and MSC-exosome (Exo) groups. Yellow and red arrows in panel F indicate starting (0 min) and ending (60 min) points, respectively. The representative time-lapse microscopic images (F) were acquired from 24h after soma application of the exosomes, whereas quantitative data (G) were acquired for 24 and 48h after exosome application. *p<0.05 vs control. Sample size in G represents the number of the growth cone from every independent experiment.

Journal: Molecular neurobiology

Article Title: Exosomes derived from mesenchymal stromal cells promote axonal growth of cortical neurons

doi: 10.1007/s12035-016-9851-0

Figure Lengend Snippet: A histogram (A) shows particle sizes of MSC-exosomes analyzed by the qNano system. Western blot analysis (B) shows the proteins of Alix and Hsp70 in MSC-exosomes (Exo) and supernatants (Sup). The schematic of a microfluidic culture device and a representative immunofluorescent image (C) show the pNFH+ cortical neurons and axons (green) in the cell body compartment (soma) and pNFH+ axons (green) in the axonal compartment (axon). The compartments are connected by 450 μm long microgrooves (C, microgrooves). DAPI labeled nuclei of cortical neurons (blue) were only present in the cell body compartment (C, soma). Panels D and E show representative images of pNFH+ axons in the axonal compartment (D, green) and quantitative data of the average axonal length (E) from the control (Ctl) and MSC-exosome (Exo) groups when the exosomes were applied into the soma compartment for 24 and 48h. * p<0.001 vs control. Panels F and G show representative time-lapse microscopic images of the growth cone extension (F) and quantitative data of growth cone elongation (G) in the axonal compartment during 60 min from the control (Ctl) and MSC-exosome (Exo) groups. Yellow and red arrows in panel F indicate starting (0 min) and ending (60 min) points, respectively. The representative time-lapse microscopic images (F) were acquired from 24h after soma application of the exosomes, whereas quantitative data (G) were acquired for 24 and 48h after exosome application. *p<0.05 vs control. Sample size in G represents the number of the growth cone from every independent experiment.

Article Snippet: The cortical neurons were then seeded in a microfluidic culture device (Standard Neuron Device, Cat# SND450, Xona Microfluidics, Temecula, CA) at density at 3×10 7 cells/ml (~3×10 5 cells in the somal compartment).

Techniques: Western Blot, Labeling, Control