• TC treated - plasma etched for adherent cells
• Vented polypropylene cap with 0.22um PTFE filters for gas exchange
• 30-50mL per layer recommended working volume
• Frosted writing area
• Clear lot number printed on each flask for traceability
• Ultrasonically welded layers, no extractable or leachable adhesives used
Quality you can rely on:
• cGMP Compliant (21 CFR part 820)
• USP grade VI virgin polystyrene flask
• USP grade VI virgin polypropylene caps
• USP grade VI virgin PTFE filter membrane
• Produced in ISO 13485:2016 and ISO 9001 facility
• Molded and packed in ISO 7 cleanroom
• E-beam sterilized and lot tested to SAL 10^-6
• Lot tested free of pyrogens USP 85
• Lot tested free of cytotoxins/pyrogens In Vivo USP 88 and In Vitro USP 87
• Lot tested free DNase/RNase and DNA
• Lot tested free BSE/TSE
• Certified free of animal products
Use Guide：
1、Mix cell suspension with medium: Prepare cell suspension of required concentration in a container. Recommended volume is about 30- 50mL per layer.
2、Add the mixed liquid into the Multi-layer Flask slowly with serological pipettes. To avoid foam and bubbles, allow liquid stream to flow along the slope of the Multi-layer Flask. (Save a little
liquid in pipette each time.)
3、Tips: A 10 mL pipette allows media to be dispensed at the bottom of the vessel. A 25 mL pipette allows media to be dispensed just past the NEST Logo.
4、Hold the Multi-layer Flask upright with the Logo facing you and tilt clockwise to a 45° angle on a flat work surface to partition the liquid into each layer.
5、While holding the Multi-layer Flask at a 45° angle, gently lay it flat onto the work surface with logo facing up.
6、After placing the Multi-layer Flask flat on a work surface, gently rock back and forth and side-to-side to distribute cells evenly onto culture surfaces.
7、Tips: Be careful to avoid foaming of medium, and not to spill liquid from each layer.
8、Repeat Step 3 to put the flask quickly and slightly into the incubator . Then, lay it flat as shown in Step 4. You may choose to either aspirate or pour the media from Multi-layer Flask.
9、Aspirating method: To aspirate or remove media, tilt Multi-layer Flask, with the NEST Logo facing you, counter-clock wise to a 45° angle while inverting the Multi-Flask toward you. Then,
tilt Multi-layer Flask to the right, continuing to aspirate all residual media.
10、Pouring method: With Logo facing you, pour spent media from Multi-layer Flask
11、Tips: Aspirate media using a NEST 2 mL or 10mL aspirating pipette.
12、Wash with buffer for one time and add dissociating reagent (≥5mL per layer). Then, follow Steps 3-4 to distribute to dissociating reagent to each layer.
13、Neutralize with inactivating solution and mix following Steps 3-4. Gently swirl to dislodge cells completely.
14、Follow Step 7 “Aspirating Method” protocol and collect cell suspension using a NEST 10mL serological pipette.
15、Follow Step 8 “Pouring Method”. Pour the cell suspension into a NEST conical tube.
16、Rinse with additional wash buffer if needed.
17、Search "NEST Multi-layer Flask" video on NEST website or Youtube.
