Quick-Neuron™ Dopaminergic - mRNA Kit

This kit differentiates human pluripotent stem cells into dopaminergic neurons in 10 days using synthetic mRNA.
DA-mRNA
As low as $349.00
The Quick-Neuron™ Dopaminergic - mRNA Kit facilitates rapid and efficient differentiation of human iPS or ES cells into dopaminergic neurons in just 10 days. Our proprietary transcription factor-based stem cell differentiation method uses synthetic mRNAs to produce highly pure populations of neurons without a genetic footprint. Quick-Neuron™ Dopaminergic differentiated cell cultures display typical neurite outgrowth and express a variety of neuronal markers, such as TUBB3 (pan-neuronal) and TH (dopaminergic).
More Information
Short Description This kit differentiates human pluripotent stem cells into dopaminergic neurons in 10 days using synthetic mRNA.
Product Components Small: QN1-mRNA, QN2-mRNA, Component N, Component P, Component D4, Component D5, Component D6, and Coating Material A
Storage Conditions mRNA should be stored at -80°C. All other components can be stored at -20°C or -80°C.
Product Use This product is for research use only. It is not approved for use in humans or for therapeutic or diagnostic use.
Differentiation Method Transcription factors delivered by synthetic mRNA
Cell Type Dopaminergic Neurons
Shipping Conditions Dry ice
Shelf Life 1 year

What kind of transcription factors are used for differentiation induction?

It is a proprietary formulated RNA and cannot be disclosed.


Why does a reagent in my differentiation kit have less than the required volume?

For reagents supplied in small volumes, be sure to briefly centrifuge before use. If pipettors have been calibrated recently and the volume is less than it is supposed to be even after the tube is spun down, please contact us at [email protected]


What should I do if I find on day 1 that cells were accumulated in the center of the well?

It is not recommended to start mRNA-based differentiation induction because the differentiation efficiency is expected to be quite low. For successful differentiation using our mRNA-based methods including Mesendoderm Booster, hPSCs should be evenly distributed in the well. It is likely that the plate was shaken too much, and cells were accumulated in the center of the well while they were floating. Next time, please handle the plate more gently or it can be left on a flat bench top without vibration for 15 min before it is put inside a CO₂ incubator.


What should I do if I find on day 1 that my culture was seeded only in the center but not in the periphery of the well?

Unless cells are accumulated in the center of the well, the instructions can be followed since this is an issue of coating. We have observed that 4-well plates available from Nunc sometimes do not allow cells to settle down in the periphery of the well when our coating conditions are applied. Next time, please use a 24-well plate and try the following: 1) incubate the plate with Coating Material A at 4°C overnight instead of 37°C for 2 hours, 2) do not aspirate the supernatant completely or leave the supernatant just enough to cover the well bottom surface after coating with Coating Material A is completed and 3) do not touch the bottom of wells with fingers when handling the plate.


I plated cells as instructed, so why does my culture look less confluent than the one shown in the user guide on day 1?

hPSCs were likely damaged while they were harvested. Ideally, hPSCs should be lifted only by pipetting several times using Solution D1 as instructed in the user guide. Even if pipetting 15 times does not lift all of the cells in the culture, do not attempt to do more pipetting but collect only cells that come off. Instead rinse the culture with PBS and start Solution D1 treatment again but with longer incubation (up to 20 minutes). Next time please reduce the concentration of the substrate used to coat the dish/well for the maintenance of the source hPSCs to 50-70%.


Why do I see many floating cells and/or cellular debris on day 1?

hPSCs were likely damaged while they were harvested. hPSCs may have been mechanically harvested by scraping or were pipetted too much or too vigorously. Lift Solution D1-treated hPSCs only by pipetting them up and down up to 15 times.


Why does my culture have colonies that appear balled up and round on day 1?

It could be that Coating Material A was diluted at room temperature or diluted using PBS warmed to room temperature. Keep both Coating Material A and PBS on ice before dilution.


Can I use Geltrex or Matrigel as a coating substrate for hPSC cultures?

Our kits are not optimized with these substrates. However, if your hPSC differentiation protocols are already optimized with such a substrate, you may try using one of these with our kit at your own risk.


I was able to harvest more hPSCs than I needed for the kit. Can I replate or freeze the leftover hPSCs to maintain their culture?

No. If you’re following the instructions given in the user guide, the hPSCs will be harvested in a differentiation medium so the leftover hPSCs cannot be maintained.


Why are there many aggregates after harvesting hPSCs?

After harvesting hPSCs, cells should not be left in the collection tube for more than 5 minutes. Leaving cells for a longer period may cause the formation of cellular clumps which interferes with infection. Single cells are best for infection.


Why doesn’t Solution D1 dissociate my hPSC culture without scraping?

The concentration of the substrate used to coat the dish/well was likely too high, so Solution D1 treatment requires longer incubation than 10 minutes (up to 20 minutes). Next time, please reduce the concentration of the substrate to 50-70%.


Why do differentiation kits require hPSCs be maintained under StemFit or StemFlex conditions?

hPSCs should be adapted to passaging as single cells prior to differentiation. Our protocols have only been tested with StemFit/StemFlex, so we can't guarantee results using other culture conditions.


How long do I need to maintain hPSCs prior to beginning to use your kit?

Before beginning differentiation, cultures should be healthy and displaying typical morphologies (i.e., round colonies with tightly packed cells exhibiting a small cytoplasmic area), few spontaneously differentiating cells, and normal growth rates (i.e., doubling once a day). We recommend growing the cells for at least 14 days post-thaw before differentiating and not allowing the cultures to reach more than 80% confluency.


Do I need a license agreement for any of Elixirgen Scientific’s products?

No. You don't need any licence or material transfer agreement (MTA) to use our differentiation kits or iPSC-derived cells. However, please be advised that these products are for research use only.


What kind of RNA is used for differentiation induction?

It is a proprietary formulated RNA and cannot be disclosed.