rpc00101: Daucus carota NC cell suspension culture
Domestic delivery: A 50-mL plastic conical centrifuge tube, containing cell suspension
Overseas delivery: A 250-mL plastic Erlenmeyer flask, containing cells placed on semi-solid medium
Subculture the cells to fresh medium immediately after arrival.
Do not store the cell culture in a refrigerator and a freezer.
Maintain aseptic conditions of the cell culture, and work in a laminar flow cabinet.
Culture medium: MS medium, 1 mg/L 2,4-D, pH 5.7 (medium no. 27)
Culture conditions: 27°C, dark, 110 rpm
Subculture: 14-day intervals
Citation of cell line
When results obtained by using this cell line are published in a scientific journal, it should be cited in the following manner: “Daucus carota NC cell line (rpc00101) was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan.”
Carrot NC cell line was established from a hypocotyl of Daucus carota L. cultivar US-Harumakigosun (Satoh et al. 1986 ). The NC is a non-embryogenic cell line that has been lost embryogenic competence during long-term culture of embryogenic suspension cells (Satoh 1998 ). The NC cells are grown in a Murashige and Skoog (MS) medium supplemented with 1 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D), pH 5.7. Our NC cell culture has been maintained in the dark at 27°C with rotary shaking at 110 rpm and subcultured at 14-day intervals.
Chemicals and stock solutions
(All stock solutions are stored at 4°C)
MS salt mix
Murashige and Skoog Plant Salt Mixture, FUJIFILM Wako Pure Chemical Corporation (#392-00591)
2,4-D (0.2 mg/mL)
2,4-D sodium monohydrate
(2,4-Dichlorophenoxy)acetic acid sodium salt monohydrate, Sigma-Aldrich (D6679)
KOH (1 N)
Erlenmeyer flask (300 mL), capped with two layers of aluminum foil
Pipette (10 mL; large tip opening) and a bulb, sterilized by autoclaving at 121°C for 20 min
Preparation of MS medium (medium no. 27)
Dissolve the following chemicals in approximately 800 mL of distilled water.
MS salt mix
1 bag (1 L)
Add following stock solutions, and fill up to approximately 950 mL with distilled water.
2,4-D (0.2 mg/mL)
Adjust the pH of the solution to 5.7 with KOH (1 N), and fill up to 1 L with distilled water.
Pour 100 mL of the medium into a 300-mL flask.
Autoclave the flask at 121°C for 20 min.
Agitate a 14-day-old culture well and transfer 5 mL of cell suspension to 100 mL of fresh MS medium with a pipette.
Incubate cell cultures on a rotary shaker at 110 rpm under the dark condition at 27°C.
For domestic customers: We send NC cell suspension in a 50-mL disposable conical centrifuge tube. The cells should be transferred to fresh MS medium immediately after arrival. Transfer settled cells to Erlenmeyer flasks containing fresh liquid medium with a pipette.
For overseas customers: We send NC cells placed on semi-solid MS medium in a 250-mL disposable Erlenmeyer flask. The cells should be transferred to fresh MS medium immediately after arrival. Collect the cells from the semi-solid medium with a spatula and transfer them to Erlenmeyer flasks containing fresh liquid medium.
In order to maintain NC cell suspension cultures stably, it is essential to transfer an adequate amount of cells to fresh MS medium in every subculture. The amount of cells may vary from one lab to another, because proliferation of NC cells is affected by culture conditions, such as a room temperature, rotation speed of a rotary shaker, and aeration condition of the culture.
In order to obtain good aeration of a suspension culture, a silicone sponge plug may be used instead of the aluminum foil cap (e.g., cap-type Silicosen; Shin-Etsu Polymer, Tokyo, Japan).