C57 Brain Striatum Neurons [Mouse]
[CAT#: NCC20-9PZ53]
Cryopreserved ampule of Mouse C57 Striatum Neurons containing ≥ 4 million cells
- Species:
- Mouse
- Applications:
- Cell Assay
- Cell Types:
- Neuron
Certificate of Analysis Lookup
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number
Description
The ready-to-use mouse C57 brain striatal neurons (M-CP-302) were separated from the mouse C57 black brain (E14, 15). These are all cell suspensions of high-quality primary embryonic brain neuron cells (including glial cells) prepared by standardized methods and can be cultured immediately.
Each vial striatal cell contains approximately 4 million living cells. Using the recommended seeding density and medium, seed it into 6 or more wells of a 24-well plate and 30 or more wells of a 96-well plate. After about 4 days of culture, the cells will form a network of neurites, and by day 7, fragmentation will be minimized.
Recommended medium: CocKit™ Primary Neuron Growth Medium (NCC20-9PZ10)
Each vial striatal cell contains approximately 4 million living cells. Using the recommended seeding density and medium, seed it into 6 or more wells of a 24-well plate and 30 or more wells of a 96-well plate. After about 4 days of culture, the cells will form a network of neurites, and by day 7, fragmentation will be minimized.
Recommended medium: CocKit™ Primary Neuron Growth Medium (NCC20-9PZ10)
Cell Types
Neuron
Applications
Cell Assay
Application Notes
• Guaranteed through 10 population doublings
• Positive immunofluorescence staining for glial fibrillary acid protein (GFAP)
• Positive immunofluorescence staining for glial fibrillary acid protein (GFAP)
Relevant Diseases
Alzheimer's Disease; Parkinson's Disease
Research Areas
Neurotoxicity; Neurogenesis
Species
Mouse
Size
≥ 4,000,000 cryopreserved cells per ampule
Form
Cryopreserved
Shipping
Dry Ice
Storage
Liquid nitrogen
Handling Advice
Frozen cells:Upon receipt, frozen ampoules should be transferred directly to gaseous phase liquid nitrogen without delay, unless they are to be used straight away.
Growing cells: Growing cell cultures should be checked on receipt using an inverted microscope. Immediately check the cell density upon arrival for any obvious defects. If the cell density is too high (more than 80% confluent) subculture the cells (harvest and reseed) immediately.
For detailed instructions on the thawing procedure of frozen cells and the culture of adherent or suspended cells, please feel free to contact us by email or phone.
Growing cells: Growing cell cultures should be checked on receipt using an inverted microscope. Immediately check the cell density upon arrival for any obvious defects. If the cell density is too high (more than 80% confluent) subculture the cells (harvest and reseed) immediately.
For detailed instructions on the thawing procedure of frozen cells and the culture of adherent or suspended cells, please feel free to contact us by email or phone.
Research Use Only
For research use only, not for diagnostic or therapeutic use.
Quality Control
• Test negative for mycoplasma, bacteria, yeast, and fungi
• HIV-1, Hepatitis B and Hepatitis C are not detected for all donors and/or cell lots
• A Certificate ofAnalysis is provided for each cell lot purchased
• HIV-1, Hepatitis B and Hepatitis C are not detected for all donors and/or cell lots
• A Certificate ofAnalysis is provided for each cell lot purchased
Neural Cell Lines
For Research Use Only. Not For Clinical Use.
