Find the Abcam 3T3-L1 differentiation protocol, ab287843.
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What Notos does today
- 01
Reads the whole protocol.
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- 02
Hands-free at the bench.
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- 03
Remembers what really happened.
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Notos turns each step into a picture with its key numbers, big enough to read with gloves on, from across the bench.
- 1.To initiate differentiation, culture cells until ~80% confluent.
- 2.Replace medium with fresh preadipocyte medium and incubate an additional 48 hrs.
- 3.Add 1 μl of Differentiation Cocktail to 1 ml of DMEM/F12 (1:1) with 10% FBS. Make enough differentiation medium as needed. Sterilize with a 0.22 μM syringe filter. Replace preadipocyte medium with differentiation medium.
- 4.Incubate for 3 days in a humidified incubator at 37°C with 5% CO2.
- Differentiation Cocktail 1 μl
- DMEM/F12 (1:1) 1 ml
- 10% FBS
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Experimental Context · Voice · Actions · Video
- t
- 00:12:47.3
- action
- dispense
- object
- tube A3
- reagent
- Buffer A
- volume
- 1.0 mL · rep 3 of 5
- step
- 2 / 7 · Add 5 mL Buffer A
- hand
- right · P1000 grip · 21 keypoints
- voice
- “Adding buffer A to tube three.”
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