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Gibco™
Medio Neurobasal™
El medio Neurobasal es un medio basal diseñado para el mantenimiento a largo plazo y la maduración de neuronas prenatalesMás información
| Número de catálogo | Cantidad |
|---|---|
| 21103049 | 500 mL |
Número de catálogo 21103049
Precio (EUR)
86,50
Each
-
Cantidad:
500 mL
Precio (EUR)
86,50
Each
El medio Neurobasal es un medio basal diseñado para el mantenimiento a largo plazo y la maduración de neuronas prenatales y embrionarias puras sin necesidad de una capa de alimentación de astrocitos cuando se utiliza con suplementos Gibco B-27.
El medio Neurobasal es adecuado para su uso en la mayoría de las aplicaciones de células neuronales. Para otras aplicaciones, ofrecemos formulaciones alternativas de medios Neurobasal y suplementos B-27.
Para protocolos establecidos que usen medios Neurobasal, acceda a nuestro manual de protocolos de neurobiología Gibco.
Vea las publicaciones que utilizan productos de neurobiología Gibco en nuestra CellCite Gibco.
El medio Neurobasal es adecuado para su uso en la mayoría de las aplicaciones de células neuronales. Para otras aplicaciones, ofrecemos formulaciones alternativas de medios Neurobasal y suplementos B-27.
Para protocolos establecidos que usen medios Neurobasal, acceda a nuestro manual de protocolos de neurobiología Gibco.
Vea las publicaciones que utilizan productos de neurobiología Gibco en nuestra CellCite Gibco.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Tipo de célulaCélulas neuronales
Línea de productosNeurobasal™
Tipo de productoMedio neurobasal
Cantidad500 mL
Duración de almacenamiento12 meses a partir de la fecha de fabricación
Condiciones de envíoAmbiente
Probado paraEndotoxinas, rendimiento, esterilidad, osmolalidad, pH
ClasificaciónSin suero
Culture TypeCultivo de células neuronales
FormularioLíquido
Con aditivosRojo de fenol
Unit SizeEach
Contenido y almacenamiento
Almacenar en el refrigerador (2–8 °C) y proteger de la luz.
Formulaciones de medios
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Certificados
Buscar por número de lote o por número de lote parcial
N.º de loteCertificate TypeDateCatalog Number(s)
3157167Certificate of Analysis26 jun 202521103049
3124491Certificate of Analysis06 jun 202521103049
3142746Certificate of Analysis15 may 202521103049
3137184Certificate of Analysis19 abr 202521103049
3026675Certificate of Analysis02 abr 202521103049
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SDSScientific Resources
Product Information
Preguntas frecuentes
Yes, the protein content in this product is high enough so filtering through a low protein binding filter as a 50X or 1X in solution should not be a problem.
Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.
No, it is not recommended to freeze media due to the potential of precipitates forming upon thaw. Inorganic salts and amino acids in the formulation may come out of solution when exposed to temperature fluctuations. These precipitates will not go back into solution easily once formed.
Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.
Neurobasal and Neurobasal-A media (for postnatal and adult neurons) allow for long-term maintenance of neuronal cells without the need for an astrocyte feeder layer. These media should be supplemented with either serum or a serum-free supplement, plus 0.5mM L-glutamine. B-27 supplement is a serum-free supplement that comes as a 50X concentrate in a 10ml volume. This is enough supplement for 500ml of media. Fetal, postnatal, and adult neural cultures can be grown in the appropriate Neurobasal medium supplemented with B-27 supplement .
We also have two other supplements. One is called G-5 and is for growth and expression of glial cells (normal and tumor) of astrocytic phenotype. This comes in a 1ml size, at a 100X concentration. The other supplement is called N-2 and is for growth and expression of post-mitotic neurons and tumor cells of neuronal phenotype. This comes in a 5ml size, at a 100X concentration.
For more information on Neurobasal media, search "Neurobasal" from our website home page.
Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.
The original published formulation of Neurobasal culture medium contained 10 µM L-cysteine. However, our Neurobasal media formulation contains 260 µM L-cysteine because it was shown to improve cell survival.
Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.
Neurospheres can be plated on laminin coated culture plates for neuron differentiation. The issue is that it is difficult to control the plating density of neurospheres. Alternatively, neurospheres can be dissociated into single cells and plate single cell suspension at a certain density such as 1-5 x 10^4 cells/cm2 onto laminin coated plates for neuron differentiation. For general neuron differentiation, Neurobasal+B27+N2 can be used. Growth factors such as BDNF and/or GDNF can be added into medium for improving survival of differentiating NSCs.
Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.
Citations & References (5)
Search citations by name, author, journal title or abstract text
Citations & References
Abstract
A comprehensive protocol for efficient differentiation of human NPCs into electrically competent neurons.
Journal:Journal of neuroscience methods
PubMed ID:39053772
Activation of Trk neurotrophin receptor signaling by pituitary adenylate cyclase-activating polypeptides.
Journal:J Biol Chem
PubMed ID:11784714
'Pituitary adenylate cyclase-activating polypeptide (PACAP), a neuropeptide that acts through G protein-coupled receptors, exerts neuroprotective effects upon many neuronal populations. However, the intracellular signaling mechanisms that account for PACAP''s trophic effects are not well characterized. Here we have tested the possibility that PACAP uses neurotrophin signaling pathways. We have found
Long-term culture of mouse cortical neurons as a model for neuronal development, aging, and death.
Journal:J Neurobiol
PubMed ID:11920724
A long-term cell culture system was used to study maturation, aging, and death of cortical neurons. Mouse cortical neurons were maintained in culture in serum-free medium (Neurobasal supplemented with B27) for 60 days in vitro (DIV). The levels of several proteins were evaluated by immunoblotting to demonstrate that these neurons
Axonal Transport Enables Neuron-to-Neuron Propagation of Human Coronavirus OC43.
Journal:J Virol
PubMed ID:29925652
Human coronaviruses (HCoVs) are recognized respiratory pathogens for which accumulating evidence indicates that in vulnerable patients the infection can cause more severe pathologies. HCoVs are not always confined to the upper respiratory tract and can invade the central nervous system (CNS) under still unclear circumstances. HCoV-induced neuropathologies in humans are
A Human Pluripotent Stem Cell-based Platform to Study SARS-CoV-2 Tropism and Model Virus Infection in Human Cells and Organoids.
Journal:Cell Stem Cell
PubMed ID:32579880
SARS-CoV-2 has caused the COVID-19 pandemic. There is an urgent need for physiological models to study SARS-CoV-2 infection using human disease-relevant cells. COVID-19 pathophysiology includes respiratory failure but involves other organ systems including gut, liver, heart, and pancreas. We present an experimental platform comprised of cell and organoid derivatives from
5 total citations