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Human Dopaminergic Neuron Cells

Size Price Quantity
1.0 Frozen Vial $600.00
Name of ProductsHuman Dopaminergic Neuron Cells (HDaNCs)
Catalogue NumbercAP-0057
Product FormatFrozen Vial
Cell Number more than 5x10[5] cells/vial
Human dopaminergic neuronal cells are isolated from fetal brain tissue obtained from agencies authorized to procure and distribute tissues for research. Dopaminergic neuronal cells are selected in a tyrosine free medium supplemented with a mixture of growth factors. The actively growing population of cells is tested for tyrosine hydroxylase (TH) expression by immunocytochemistry. HDaNCs cells are provided at more than 5 x 10[5] cells/vial @ Passage 1 with more than 70% TH positive. HDaNCs are grown in HDaNCs medium (supplemented with 10% FBS and growth factors, cAP-63). The cells are grown in regular tissue culture dishes coated with Matrigel Coating Solution (cAP-58) and subcultured at a split ratio of 1 to 2 at the confluence. We recommend not to use the cells beyond 4 passages. There may be a significant decrease in the number of tyrosine hydroxylase positive cells after 4 passages as they are not maintained in selective medium to allow the growth of only cells expressing tyrosine hydroxylase.
1.Tyrosine hydroxylase (TH) more than 70% positive by immunofluorescence
2.HDaNCs are negative for HIV-1, HBV, HCV, and mycoplasma.
The cells are offered for Research Use Only.
Frozen Vials in a Dry Ice Package.
When you receive the dry ice package with cells in frozen vials, transfer the frozen vials of cells into a -80C freezer for short period storage or a liquid nitrogen tank for long- term storage.
A)Pre-coating of T25 flasks- Add 2ml each Matrigel Coating Solution (cAP-58) into a T25 flask to cover the whole surface of the flask, and then incubate for at least 1 hour at 37C. Aspirate the excessive coating solution shortly before the inoculation of the cells.
B)Thaw the frozen cell vial in a 37C water bath first, and then transfer the cells into the pre-coated T25 flask with 10ml of HDaNCs medium. Change the medium after overnight and then every two days. The cells usually become confluent within 5-7 days.
C)To passage the cells, rinse the cells in a T25 flask with 5ml HBSS (RT) twice; then add 2ml Trypsin/EDTA (RT) (cAP-23) into one T25 flask; gently dispose the excessive Trypsin/EDTA solution within 20 seconds by aspiration.
D)Leave the T25 flask with the cells at RT or 37C for 1 min (most cells usually will detach from the surface within 1-2 mins; or monitor the cells under a microscope until most of cells become rounded up, and then gently tap the flask against the bench surface, and the cells will move on the surface of the flask when monitoring under microscope.
E)Add 5ml Trypsin Neutralization Buffer and spin down the cells with 800g centrifugation for 5 mins.
G)Re-suspend the cell pellet with 10 or 15ml Full medium and transfer 5 ml each into 2 or 3 pre-coated T25 flasks (for 1/2 to 1/3 subculture ratio).
H)Change medium every 2 or 3days and the cells usually become confluent within 7 days (when split at a 1/3 ratio).
Quick Coating SolutioncAP-01
HDaNC Growth MediumcAP-63
HBSS w/o Ca2+, Mg2+cAP-11
Cell Freezing Solution (FBS)cAP-22
Cell Freezing Solution (Non-FBS)cAP-22B
Trypsin/EDTA SolutioncAP-23
Trypsin Neutralization SolutioncAP-28
ITS (100x)cAP-26
L-Glutamine-MAXIMUM (100x) cAP-27
Human Plasma Fibronectin SolutioncAP-42
Handling human tissue derived products is potentially bio-hazardous, despite tested negative for HIV, HBV and HCV DNA; nonetheless, proper precautions must be taken to avoid inadvertent exposure.