PCS-450-011 ™
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HepatoXcell™ Pro are Primary Human Hepatocytes, 7 day Plateable, derived from normal, healthy, human liver tissues.
Use promo code ATCC‑000062 to get 10% off 1–5 vials of HepatoXcell™ Pro or Plus when you purchase at least 1 bottle of Thawing Medium, Plating Medium, and Maintenance Medium.
Use promo code ATCC-000058 to get 20% off when purchasing 20 vials or more of Hepatocyte cells.
ATCC determines the biosafety level of a material based on our risk assessment as guided by the current edition of Biosafety in Microbiological and Biomedical Laboratories (BMBL), U.S. Department of Health and Human Services. It is your responsibility to understand the hazards associated with the material per your organization’s policies and procedures as well as any other applicable regulations as enforced by your local or national agencies.
ATCC highly recommends that appropriate personal protective equipment is always used when handling vials. For cultures that require storage in liquid nitrogen, it is important to note that some vials may leak when submersed in liquid nitrogen and will slowly fill with liquid nitrogen. Upon thawing, the conversion of the liquid nitrogen back to its gas phase may result in the vial exploding or blowing off its cap with dangerous force creating flying debris. Unless necessary, ATCC recommends that these cultures be stored in the vapor phase of liquid nitrogen rather than submersed in liquid nitrogen.
Unpacking and storage instructions
Required media and supplement
• One bottle of each of the following: Hepatocyte Thaw Media (ATCC PCS-450-032), Hepatocyte Plating Media (ATCC PCS-450-038), Hepatocyte Maintenance Media (ATCC PCS-450-034). Cell Basement Membrane (ATCC ACS-3035). Optional media supplements: Penicillin-Streptomycin-Amphotericin B Solution (ATCC PCS-999-002)
Handling procedure
1. Refer to the batch specific information for the total number of viable cells recovered post-thaw for any lot of PCS-450-011.
2. Add 19 mL of pre-warmed Hepatocyte Thaw Media to a 50 mL centrifuge tube.
3. Remove one vial of PCS-450-011 from storage and thaw the cells by gentle agitation in a 37°C water bath. To reduce the possibility of contamination, keep the O-ring and cap out of the water. Thawing should be rapid (approximately 1 to 2 minutes).
4. Remove the vial from the water bath as soon as the contents are thawed leaving a small ice pellet and decontaminate by dipping in or spraying with 70% ethanol. All operations from this point onward should be carried out under strict aseptic conditions.
5. Gently pour the contents of the vial into the 50 mL centrifuge tube.
6. Using a wide bore pipette tip wash the vial with 1 mL of the Hepatocyte Thaw Media suspension to retrieve any cells left in the vial.
Note: When pipetting Hepatocytes NEVER pipette up and down to mix, instead gently rock or shake the tube.
7. Centrifuge at 100 x g for 10 minutes.
8. Carefully remove the supernatant and resuspend with 1 mL of prewarmed Hepatocyte Plating Media.
9. Gently rock or shake the tube to resuspend the cells, then add an additional 1 mL of Hepatocyte Plating Media.
10. Mix gently by rocking or shaking to ensure a homogenous suspension.
11. Perform a cell count using the Trypan Blue Exclusion Method.
12. Using the total number of viable cells, dilute the cells to 800,000 cells/mL.
13. Seed one well in a Collagen I coated 24-well plate with 500 µL of the cell suspension.
14. Gently shake plate in a “T” motion to evenly distribute the cells.
15. Under the microscope, let the cells settle to ensure seeding density is not too low or high.
16. If the seeding density is too low add 50 µL of cell suspension to the well, if too high shake the plate to resuspend cells and remove 50 µL of cell suspension.
17. After seeding density is optimized, seed remaining wells with Human Hepatocyte cell suspension.
18. Gently shake in a “T” motion and place into a 36°C ± 2°C, 5% CO2 ± 2% CO2 incubator.
19. At 1 hour post seeding gently shake the plate in a “T” motion to evenly distribute the cells and remove any dead cells attached to the plate wells.
20. At 2 hours post-seeding gently shake the plate in a “T” motion and perform a media change using pre-warmed plating media to remove excess dead cells.
21. Four to six hours post-seeding, perform a media change with cold Hepatocyte Maintenance Media supplemented with 0.3 mg/mL Cell Basement Matrix.
22. Put plate back into incubator and change media daily.
The product is provided 'AS IS' and the viability of ATCC® products is warranted for 30 days from the date of shipment, provided that the customer has stored and handled the product according to the information included on the product information sheet, website, and Certificate of Analysis. For living cultures, ATCC lists the media formulation and reagents that have been found to be effective for the product. While other unspecified media and reagents may also produce satisfactory results, a change in the ATCC and/or depositor-recommended protocols may affect the recovery, growth, and/or function of the product. If an alternative medium formulation or reagent is used, the ATCC warranty for viability is no longer valid. Except as expressly set forth herein, no other warranties of any kind are provided, express or implied, including, but not limited to, any implied warranties of merchantability, fitness for a particular purpose, manufacture according to cGMP standards, typicality, safety, accuracy, and/or noninfringement.
This product is intended for laboratory research use only. It is not intended for any animal or human therapeutic use, any human or animal consumption, or any diagnostic use. Any proposed commercial use is prohibited without a license from ATCC.
While ATCC uses reasonable efforts to include accurate and up-to-date information on this product sheet, ATCC makes no warranties or representations as to its accuracy. Citations from scientific literature and patents are provided for informational purposes only. ATCC does not warrant that such information has been confirmed to be accurate or complete and the customer bears the sole responsibility of confirming the accuracy and completeness of any such information.
This product is sent on the condition that the customer is responsible for and assumes all risk and responsibility in connection with the receipt, handling, storage, disposal, and use of the ATCC product including without limitation taking all appropriate safety and handling precautions to minimize health or environmental risk. As a condition of receiving the material, the customer agrees that any activity undertaken with the ATCC product and any progeny or modifications will be conducted in compliance with all applicable laws, regulations, and guidelines. This product is provided 'AS IS' with no representations or warranties whatsoever except as expressly set forth herein and in no event shall ATCC, its parents, subsidiaries, directors, officers, agents, employees, assigns, successors, and affiliates be liable for indirect, special, incidental, or consequential damages of any kind in connection with or arising out of the customer's use of the product. While reasonable effort is made to ensure authenticity and reliability of materials on deposit, ATCC is not liable for damages arising from the misidentification or misrepresentation of such materials.
Please see the material transfer agreement (MTA) for further details regarding the use of this product. The MTA is available at www.atcc.org.
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