Yes, these can be stacked upon each other. Please see the helpful User Guide.
材料
angled neck high-density polyethylene cap (vented)
polystyrene flask
品質等級
無菌
sterile; γ-irradiated
特點
3 layer
包裝
pack of 16
製造商/商標名
Millicell®
參數
45 °C max. temp.
技術
cell culture | mammalian: suitable
高度
32 mm , excluding cap
51 mm , including cap
長度
22.2 cm
寬度
12 cm
表面積
600 cm2
有效容積
120-180 mL
結合類型
Tissue Culture (TC)-treated surface
運輸包裝
ambient
1 of 4
本產品 | PFHYS1008 | CLS430641 | CLS430824 |
|---|---|---|---|
| manufacturer/tradename Millicell® | manufacturer/tradename Millicell® | manufacturer/tradename Corning 430641 | manufacturer/tradename Corning 430824 |
| material angled neck high-density polyethylene cap (vented), polystyrene flask | material high-density polyethylene cap, polystyrene flask | material canted neck , cap (vented), polystyrene , rectangular flask | material canted neck , cap (phenolic-style), phenolic cap, polystyrene , rectangular bottom flask, rectangular flask |
| binding type Tissue Culture (TC)-treated surface | binding type Tissue Culture (TC)-treated surface | binding type - | binding type Tissue Culture (TC)-treated surface |
| feature 3 layer | feature 5 layer | feature graduations | feature cap, graduations |
| surface area 600 cm2 | surface area 1000 cm2 | surface area 75 cm2 | surface area 150 cm2 |
| packaging pack of 16 | packaging pack of 8 | packaging case of 100 | packaging case of 50 |
一般說明
特點和優勢
- Multilayer Design: Available in 3- and 5-layer configurations, providing a larger surface area for cell growth while maintaining a compact footprint similar to traditional T-flasks
- Enhanced Accessibility: Designed for better pipette access, accommodating larger volume pipettes (up to 25 mL)
- Increased Efficiency: Cultivate more cells in the same space, maximizing research output
- Space Optimization: Achieves significant space savings compared to other multilayer flasks on the market
準備報告
- To seed cells, fill the Millicell HY T-600 Flask with the desired growth media.
- Add desired number of cells to achieve typical seeding density.
- Mix the cells and media by raising the end of the flask and pipetting the solution up and down several times until a homogeneous suspension is achieved. Note: Failure to adequately mix cells into a homogeneous suspension may result in an uneven distribution of cells across the layers of the Millicell HY Flask.
- Briefly lay the flask on its side to equilibrate the liquid volume equally among the layers of the flask.
- Tilt the flask on its end to partition the liquid volume for each layer of the flask.
- Lay the flask down to spread the cell suspension evenly across the entire surface of each layer.
- Depending on the volume it may be necessary to rock the flask on all four corners to ensure that the entire surface wets. Note: If the liquid volume on any of the layers changes during the wetting procedure (e.g., spilling of liquid from top layer to lower layers), repeat steps 4–6 to ensure even distribution of liquid among all layers.
- Return the flask to a vertical position when transporting to the incubator. Lay the flask flat in the incubator (as in step 6) and culture cells under appropriate conditions.
- If media exchange is required, either aspirate or pour the media from the Millicell HY T-600 Flask. Note: Due to the larger surface area of the Millicell Flasks, it may be necessary to let the flask stand on its side for several minutes following each aspiration so that all residual liquid pools to a common point, allowing for a second aspiration to completely remove the remaining liquid.
- Add appropriate volume of fresh media, and repeat steps 4–8.
- To harvest cells, remove media as in step 9.
- Add desired amount of appropriate wash solution (e.g., PBS or 0.02% EDTA) to the flask and repeat steps 4–7.
- Remove wash solution as in step 9.
- Add desired amount of dissociation enzyme (e.g., 0.25% trypsin/EDTA or equivalent) according to preferred protocol, repeat steps 4–8, and incubate. Volume of dissociation enzyme required per cm2 does not need to be altered from T-flask protocol. Note: Ensure that all cells have completely dissociated from the surface of the flask via observation under microscope. Failure to allow complete dissociation of cells from culture surface (such that all cells are freely floating) may result in reduced cell yields.
- If using trypsin, add desired volume of inactivating solution, such as serum-containing media.
- Collect cells either by aspirating or pouring, as in step 9.
法律資訊
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
相關內容
Monitor your cell cultures with ease with the Millicell® DCI Digital Cell Imager. From confluency to cell count and morphology, the Millicell® DCI automates cell culture measurements for quicker, more consistent culturing.
使用 Millicell® DCI 數位細胞成像儀輕鬆監控您的細胞培養。Millicell® DCI 可自動進行細胞培養測量,從匯合度到細胞數量和形態,讓培養更快速、更一致。
Millicell® HY Multilayer Culture Flasks Enable Higher Cell Recovery and Space Savings Compared to Other Multilayer Flasks
Successful delivery of nucleic acids and protein in eukaryotic cells requires a transfection protocol that maximizes transfection efciency, minimizes cytotoxicity, and results in the desired level of gene expression or silencing. EMD Millipore recognizes that there is not a one-size-ts-all solution to your transfection needs. We provide the breadth of transfection reagents necessary to give you the freedom to design the perfect experiment.
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Can these 5 layer flasks be stacked atop each other?
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