Primary Human Small Intestine Microvascular Endothelial Cells (HSIMVECs)

We are excited to introduce our exceptional product, the Primary Human Small Intestine Microvascular Endothelial Cells (HSIMVECs), available under catalog number UBP015. These remarkable cells are derived from normal human small intestine tissue and are conveniently provided in frozen vials at passage 1 or T-25 flask format. Each vial contains over 5x10^5 cells, ensuring an ample supply for your research needs.

For optimal cell culture, we recommend utilizing our Universal Endothelial Growth Medium (UEGM), supplemented with 10% serum and growth supplements. These cells exhibit an impressive minimum average population doubling level of >16 when cultured as per the detailed protocol provided.

Notably, the cell characteristics include cytoplasmic VWF/Factor VIII, Di-I-Ac-LDL, and PECAM1, each demonstrating over 95% positivity by immunofluorescence. Furthermore, our HSInMVEC cells have been rigorously tested and are confirmed negative for HIV-1, HBV, HCV, and mycoplasma.

Please note that these cells are designated for research purposes only. When shipping, the frozen vials are carefully packaged with dry ice to maintain their integrity during transit.

Upon receipt of the frozen vials, promptly transfer them into a -80°C freezer for short-term storage or a liquid nitrogen tank for long-term preservation. Thank you for considering our exceptional HSIMVECs for your research endeavors.

Cell culture instructions for a T-25 flask:

1. Ensure that the flask is at 90% confluence. If not, remove the transport medium and add 5 ml of fresh media to the flask. Place the flask in a 37°C incubator until the cells reach 90% confluence, changing the media every 2 days.

2. If the flask is at 90% confluence, remove the transport media from the flask.

3. Rinse the T-25 flask containing cells with 5 ml 1X PBS.

4. Gently aspirate out the 1X PBS after rinsing and discarding.

5. Add 2 ml of room temperature Universal Detachment solution to the T-25 flask containing cells, ensuring that the entire interior surface is covered.

6. Place the T-25 flask containing cells into a 37°C incubator for 1 or 2 minutes. Cells will normally come off the surface within 1 or 2 minutes.

7. Suspend the cells with 15 ml of Universal ENDO-Growth Medium and transfer them equally into 3 pre-coated T-25 flasks (the cells are now at a subculture ratio of 1:3).

8. There is no need to spin cells during subculture when Universal Cell Detachment solution is used.

9. For proliferating cell culture, change the Universal ENDO-Growth medium every 2 days. The cells normally become confluent within 7 days when split at a 1:3 ratio.

10. Use ENDO-Basal media containing 0.5% FBS to induce quiescent cells (after 18-24 hours).

Welcome to the Thawing and Subculture Protocols to ensure optimal cell culture techniques and successful experiments.

A) Pre-coating of T-25 flasks:

Prepare the T-25 flask for cell culture by applying 2ml of Universal Coating Solution, ensuring full coverage. After 5 minutes, carefully remove any excess coating solution and rinse the flask twice with 5ml of 1x PBS. Your flask is now primed and ready for use.

B) Thawing the cells:

Thaw the frozen cell vial in a 37°C water bath, leaving a small amount of ice in the vial. Then, transfer the cells into the pre-coated T-25 flask with 10ml of growth medium. Usually, the cells will reach confluency overnight and be ready for passage within a few days.

C) Subculturing the cells:

Start by rinsing the cells in a T-25 flask with 5ml of room-temperature 1xPBS, followed by adding 2ml of room-temperature Universal Detachment Solution into the flask. Gently dispose of the excess solution within 20 seconds by aspiration.

D) Detaching the cells:

Leave the T-25 flask with the cells in a 37°C incubator for 1 minute. Most cells usually detach from the surface within 1-2 minutes. Alternatively, you can monitor the cells under a microscope until most of them become rounded up. Then gently tap the flask against the bench surface, and the cells will move on the surface of the flask when observed under a microscope.

E) Centrifugation:

Add 5ml of Universal Neutralization Buffer and spin down the cells with an 800g centrifugation for 5 minutes.

F) Re-suspending the cells:

Re-suspend the cell pellet with 10 or 15ml of Universal Growth Medium and transfer 5ml each into 2 or 3 pre-coated T25 flasks for a 1/2 to 1/3 subculture ratio.

G) Maintenance:

Ensure the medium is changed every 2 or 3 days, and the cells usually reach confluency within 7 days when split at a 1/3 ratio.

H) Preparation for experiments:

For experiments, to prepare quiescent cells, replace with Universal Endothelial Basal Medium containing 0.5% FBS when the cells are nearly confluent for about 8-12 hours before your experiments.

These protocols are designed to support the growth and health of your cells, ensuring the success of your important research.