JPH06233671A - Culture container - Google Patents

Culture container

Info

Publication number
JPH06233671A
JPH06233671A JP5020217A JP2021793A JPH06233671A JP H06233671 A JPH06233671 A JP H06233671A JP 5020217 A JP5020217 A JP 5020217A JP 2021793 A JP2021793 A JP 2021793A JP H06233671 A JPH06233671 A JP H06233671A
Authority
JP
Japan
Prior art keywords
main body
side wall
culture container
culture
lid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP5020217A
Other languages
Japanese (ja)
Other versions
JP2740611B2 (en
Inventor
Kanehisa Yokoyama
兼久 横山
Akinori Akamine
昭則 赤嶺
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP5020217A priority Critical patent/JP2740611B2/en
Publication of JPH06233671A publication Critical patent/JPH06233671A/en
Application granted granted Critical
Publication of JP2740611B2 publication Critical patent/JP2740611B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M23/00Constructional details, e.g. recesses, hinges
    • C12M23/02Form or structure of the vessel
    • C12M23/08Flask, bottle or test tube

Abstract

PURPOSE:To obtain a culture container capable of performing pipet operation or scraping operation without impairing the airtightness as the container and causing a dead angle in operation after the culturing and surely and readily recovering a cell, etc. CONSTITUTION:This culture container is composed of a body part 1 composed of a bottom wall 3 and sidewalls 4, surrounding the bottom wall and having a neck part 5 to be an opening therein and a lid part 2 engaged with the tops of the sidewalls parallel to the bottom wall. The engaging part of the body part with the lid part is detachably and temporarily bonded.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、細菌培養、細胞培養、
組織培養などに用いられる、プラスチック製でディスポ
ーザブルの培養容器に関するものである。
The present invention relates to bacterial culture, cell culture,
The present invention relates to a plastic, disposable culture container used for tissue culture and the like.

【0002】[0002]

【従来の技術】本発明が対象とする培養容器は一般に培
養用フラスコと呼ばれ、細菌培養、細胞培養、組織培養
などの分野で汎用されている。特に、細胞培養の分野で
は、培養用ディッシュや培養用プレートと並んで広く使
用されている。この培養用フラスコが使われる由縁は、
頚部にキャップをすることによりほぼ密封状態となり、
培養中の取扱が容易であり、培養用ディッシュのように
持ち運びの際に培地がこぼれる恐れがなく、又、外から
の雑菌の侵入の危険性が少ないことにある。
2. Description of the Related Art A culture container targeted by the present invention is generally called a culture flask and is widely used in the fields of bacterial culture, cell culture, tissue culture and the like. In particular, in the field of cell culture, it is widely used along with culture dishes and culture plates. The reason why this culture flask is used is
By putting a cap on the neck, it becomes almost sealed,
It is easy to handle during culturing, there is no risk of spilling the medium when carrying it like a dish for culturing, and there is little risk of invasion of foreign bacteria from the outside.

【0003】しかし、培養用フラスコの使用時には、開
口部となる頚部を通じて細胞浮遊液の注入や、培地の注
入、交換をピペットを使って行ったり、培養した細胞を
かきとり治具で剥がしたり、剥した細胞を細胞浮遊液と
してピペットで吸い取り、回収するなどの操作が行われ
る。これらの操作のうち、細胞浮遊液や培地の注入など
の培養容器の外から内への操作においては特に支障は生
じないが、培養容器の内から外、すなわち、細胞の回収
時のピペット操作やかきとり治具の操作において死角を
生じ、用具が培養容器の隅ずみまで届かないという欠点
がある。又、細い頚部を通して操作するため、数多くの
培養容器から細胞を回収する場合などは作業効率が悪
く、かなりの長時間を要すると言う問題がある。
However, when the culture flask is used, a cell suspension is injected through the neck, which is an opening, a medium is injected or exchanged with a pipette, and the cultured cells are peeled off with a scraping jig. The cells are sucked into a cell suspension with a pipette, and collected. Among these operations, there are no particular problems in operations from outside to inside the culture container, such as injection of cell suspension or medium, but from inside to outside of the culture container, that is, pipetting at the time of collecting cells or There is a drawback that a blind spot is generated in the operation of the scraping jig, and the tool cannot reach the corners of the culture container. Further, since the operation is performed through a narrow neck, there is a problem that the working efficiency is low and a considerably long time is required when cells are collected from many culture vessels.

【0004】このような欠点を補うために、頚部の開口
部の径をなるべく大きくとるような設計を行おうとして
も、容器を積みかさねてインキュベーターへ入れる場合
には、限られたスペースにより多くの培養容器を納める
必要上、培養容器本体の高さには制限が有り、そのため
開口部径も制限され大きくすることが出来ない。
In order to make up for such drawbacks, even if a design is made such that the diameter of the neck opening is as large as possible, when the containers are stacked and put in the incubator, more space is required due to the limited space. Since it is necessary to accommodate the culture container, the height of the culture container body is limited, and therefore the diameter of the opening is also limited and cannot be increased.

【0005】これらの欠点を解決する手段の1つとし
て、頚部の開口端の直径を大きくとり、かつ側壁の高さ
が高くならないように、頚部の取り付け部へ向かって上
下を狭めていくという方法(実開昭63−63400号
公報、米国特許第 4,770,854号)があるが、開口端の直
径を大きくすると、これらの容器にキャップを付けて順
に積み重ねていく上で頚部同志がお互いに邪魔し合う結
果となり、またキャップ構造の設計が難しくなり気密性
を損なう恐れが有るため、開口端を一定以上には大きく
出来ない制約がある。
As one of means for solving these drawbacks, a method of increasing the diameter of the open end of the neck and narrowing the upper and lower parts toward the attachment part of the neck so that the height of the side wall does not become high. (Japanese Utility Model Laid-Open No. 63-63400, US Pat. No. 4,770,854), but when the diameter of the open end is increased, the necks interfere with each other when the containers are capped and stacked in order. As a result, the design of the cap structure becomes difficult and airtightness may be impaired. Therefore, there is a restriction that the opening end cannot be made larger than a certain value.

【0006】そこで、培養終了後の細胞等の回収を容易
にするため、フラスコ上面の蓋部にプラスチックのシー
トを熔着しておき、培養後そのシートを剥すか切りとる
ことにより、頚部を経ずに細胞等の回収操作を行うよう
に工夫したものもある。しかし、このようにシートを蓋
部として貼った場合、シートは強度が小さいため、フラ
スコを複数個積み重ねた時不安定になり易く、積み重ね
に適さない。又、シートをカッター等で切る場合など、
カッターの刃を滅菌するなどの注意を払わないと、外部
より細菌等がフラスコ内に混入する問題もある。
[0006] Therefore, in order to facilitate the recovery of cells and the like after the completion of the culture, a plastic sheet is welded to the lid on the upper surface of the flask, and after the culture, the sheet is peeled or cut off so that it does not pass through the neck. There is also a device devised to collect cells and the like. However, when the sheet is stuck as the lid in this way, the sheet is weak in strength, so that it tends to become unstable when a plurality of flasks are stacked, and is not suitable for stacking. Also, when cutting the sheet with a cutter, etc.
If care is not taken such as sterilizing the blade of the cutter, there is also a problem that bacteria etc. are mixed into the flask from the outside.

【0007】[0007]

【発明が解決しようとする課題】本発明は、培養用フラ
スコのこの様な現状に鑑みてなされたもので、その目的
とするところは、気密性などを損なうことなく、細胞等
の回収時におけるピペットやかきとり治具の操作を容易
にした培養容器を提供することにある。
DISCLOSURE OF THE INVENTION The present invention has been made in view of the present situation of culture flasks, and its purpose is to recover cells and the like without impairing airtightness. It is to provide a culture container in which a pipette and a scraping jig can be easily operated.

【0008】[0008]

【課題を解決するための手段】即ち本発明は、培養面と
なる底部壁とその底部壁を囲む側壁よりなり、該側壁に
は開口部となる頚部を有する本体部と、底部壁と平行に
側壁の上端部に嵌合する蓋部とで構成されるプラスチッ
クの成形品であって、両者の嵌合部が取り外し可能であ
るよう仮接着されていることを特徴とする培養容器であ
る。
Means for Solving the Problems That is, the present invention comprises a bottom wall which is a culture surface and a side wall which surrounds the bottom wall, and a main body having a neck which is an opening in the side wall, and a side wall which is parallel to the bottom wall. A culture container, which is a plastic molded product composed of a lid portion fitted to the upper end portion of the side wall, wherein the fitting portions of both are temporarily adhered so as to be removable.

【0009】以下、図面により本発明による培養容器に
ついて詳細に説明する。図1は本発明の一実施例となる
培養容器を示す図で、(a)は全体を示す斜視図、
(b)は側断面図である。
Hereinafter, the culture container according to the present invention will be described in detail with reference to the drawings. FIG. 1 is a view showing a culture container according to an embodiment of the present invention, (a) is a perspective view showing the whole,
(B) is a side sectional view.

【0010】本発明でいう培養容器とは、細胞培養、組
織培養、細菌培養などに用いられるプラスチック製の培
養用フラスコであり、培養面となる底部壁(3)とそれ
を取り囲む側壁(4)からなり、側壁(4)の一つには
使用時に試料液や培地を注入するための開口部となる頚
部(5)が設けられた容器本体部(1)と、側壁(4)
の上端部に底部壁(3)と平行に取り外し可能に嵌合、
取り付けされる蓋部(2)とで構成されている。
The culture vessel in the present invention is a plastic culture flask used for cell culture, tissue culture, bacterial culture, etc., and has a bottom wall (3) as a culture surface and a side wall (4) surrounding it. And a side wall (4) having a container body (1) provided with a neck (5) serving as an opening for injecting a sample solution or a medium at the time of use, and the side wall (4).
Removably fitted to the upper end of the parallel to the bottom wall (3),
It is composed of a lid part (2) to be attached.

【0011】本体部(1)と蓋部(2)の嵌合部は、図
2に示したように、本体部(1)の側壁(4)の上端部
の全周または一部に切欠き(6)または溝(7)を設
け、一方蓋部(2)にはその周縁部下面の、前記切欠き
(6)または溝(7)に対応する位置に凸部(8)を設
ける方法により形成されている。また、これとは反対
に、蓋部(2)の周縁部下面の全体または一部に溝
(9)を設けて、本体部(1)の側壁(4)の上端部、
または上端部の前記溝(9)に対応する位置に設けた凸
部(10)を嵌合させる方式であっても良い。これによ
って、本体部(1)と蓋部(2)とを組立てる際の位置
合せがスムーズに行なえるだけでなく、嵌合部面積を大
きくし、嵌合部の密封性、接着性をより確実にする効果
が得られる。
As shown in FIG. 2, the fitting portion between the main body portion (1) and the lid portion (2) is notched on the entire circumference or a part of the upper end portion of the side wall (4) of the main body portion (1). (6) or the groove (7) is provided, and the convex portion (8) is provided at the position corresponding to the notch (6) or the groove (7) on the lower surface of the peripheral portion of the lid portion (2). Has been formed. On the contrary, by providing a groove (9) in the whole or a part of the lower surface of the peripheral edge of the lid (2), the upper end of the side wall (4) of the main body (1),
Alternatively, a method of fitting a convex portion (10) provided at a position corresponding to the groove (9) on the upper end may be adopted. This not only allows for smooth alignment when assembling the main body part (1) and the lid part (2), but also increases the area of the fitting part and ensures the sealing and adhesiveness of the fitting part. The effect is obtained.

【0012】本体部(1)と蓋部(2)とは、シリコー
ンゴムによる仮接着により嵌合、組立てする。嵌合部の
切欠き(6)または溝(7、9)に、液状のシリコーン
ゴムを塗布もしくは充填した後、本体部(1)と蓋部
(2)とを組合せてシリコーンゴムを硬化させると、図
2および図3に示すようなシリコーンゴム層(11)が
形成され、密封接着層となる。一般にシリコーンゴム
は、疎水性であるプラスチック類とは完全には接着しな
いので、接着後も本体部(1)から蓋部(2)を容易に
取り外すことが出来る。また、蓋部(2)の長さ及び/
または幅を本体部(1)のそれより若干大きく作り、底
部壁(3)を取り囲む側壁の少なくとも一つに沿って、
図3に示すような幅0.3〜1.5mm程度の出張り(12)
を設けておけば、本体部(1)から蓋部(2)を取り外
すのに好都合である。
The body portion (1) and the lid portion (2) are fitted and assembled by temporary adhesion with silicone rubber. After the liquid silicone rubber is applied or filled in the notches (6) or the grooves (7, 9) of the fitting portion, the silicone rubber is cured by combining the body portion (1) and the lid portion (2). The silicone rubber layer (11) as shown in FIGS. 2 and 3 is formed to serve as a sealing adhesive layer. In general, silicone rubber does not completely adhere to hydrophobic plastics, so that the lid (2) can be easily removed from the main body (1) even after the adhesion. In addition, the length of the lid (2) and /
Alternatively, the width is made slightly larger than that of the main body (1), and along at least one of the side walls surrounding the bottom wall (3),
A protrusion with a width of about 0.3 to 1.5 mm as shown in FIG. 3 (12)
If it is provided, it is convenient to remove the lid portion (2) from the main body portion (1).

【0013】本体部(1)と蓋部(2)の嵌合部の両方
が疎水性であると、蓋部を取り外したとき、シリコーン
ゴム層(11)が本体部側と蓋部側のどちらに残るかは
一定しない。そこで、本体部(1)または蓋部(2)の
どちらか片方に親水化処理を施すことにより、蓋部
(2)を取り外した時に、シリコーンゴム層(11)を
確実に親水化処理を施した側に残すことが出来る。これ
により一旦、蓋部(2)を取り外しても、残ったシリコ
ーンゴム層(11)がパッキングの役目をし、再び蓋部
(2)を本体(1)に嵌合させて再使用、あるいは培養
を継続することもできる。細胞の接着性を付与する目的
で培養面である底部壁(3)に親水化処理を施す必要性
が高いことから、本体部(1)側に親水化処理を施せ
ば、1回の親水化処理ですみ工程上有利となる。
If both the main body part (1) and the fitting part of the lid part (2) are hydrophobic, the silicone rubber layer (11) will remain on either the main body part side or the lid part side when the lid part is removed. It remains uncertain whether or not it will remain. Therefore, by applying a hydrophilic treatment to either the main body portion (1) or the lid portion (2), the silicone rubber layer (11) is surely subjected to the hydrophilic treatment treatment when the lid portion (2) is removed. You can leave it on the side you did. As a result, even if the lid part (2) is once removed, the remaining silicone rubber layer (11) serves as a packing, and the lid part (2) is fitted again to the main body (1) for reuse or culture. Can also be continued. Since it is highly necessary to apply hydrophilic treatment to the bottom wall (3) that is the culture surface for the purpose of imparting cell adhesiveness, if the main body (1) side is subjected to hydrophilic treatment, it will be hydrophilized once. Processing is advantageous in terms of processing.

【0014】尚、本発明における培養用フラスコを形成
するプラスチックは、透明なものであることが必要で、
ポリスチレン、ポリエステル、ポリカーボネートなどを
用いるのが良い。キャップは透明である必要はなく、通
常キャップとして用いられるプラスチックでよい。又、
嵌合部の封止接着に用いる接着剤としては、細胞毒性の
ないことや、密封性を保持することが必要で、シリコー
ンゴムが適している。シリコーンゴムとしては、硬化前
は液状で、硬化に高温を要しない、できれば室温硬化性
のものが上記熱可塑性の樹脂に適用する点から望まし
い。
The plastic forming the culture flask in the present invention must be transparent.
It is preferable to use polystyrene, polyester, polycarbonate or the like. The cap need not be transparent and may be the plastic normally used as a cap. or,
Silicone rubber is suitable as an adhesive used for sealing and adhering the fitting portion, since it is required to have no cytotoxicity and maintain sealing property. As the silicone rubber, it is preferable to use a silicone rubber that is liquid before curing and does not require high temperature for curing, and is preferably room temperature curable, from the viewpoint of being applied to the thermoplastic resin.

【0015】[0015]

【発明の効果】本発明に従うと、培養時における培養容
器の気密性などを損なわせることなく、培養後の細胞等
の回収時には蓋部を取り外すことにより、頚部を経るこ
となく、ピペット及びかきとり治具による操作を行うこ
とが出来るので、ピペットやかきとり治具の操作上の死
角がなく、確実にしかも容易に細胞等の回収ができる培
養容器を提供することができる。
EFFECTS OF THE INVENTION According to the present invention, the pipette and scraping can be repaired without passing through the neck by removing the lid when recovering cells after culturing without impairing the airtightness of the culture container during culturing. Since the operation can be performed by the tool, it is possible to provide a culture container in which there is no blind spot in the operation of the pipette or the scraping jig and the cells and the like can be collected reliably and easily.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明における培養容器の一実施例を示す図
で、(a)は斜視図、(b)は側断面図である。
1A and 1B are views showing an embodiment of a culture container according to the present invention, in which FIG. 1A is a perspective view and FIG. 1B is a side sectional view.

【図2】本体部と蓋部の嵌合構造の一実施例を示す図で
ある。
FIG. 2 is a diagram showing an example of a fitting structure of a main body and a lid.

【図3】本体部と蓋部の嵌合構造の他の実施例を示す図
である。
FIG. 3 is a view showing another embodiment of the fitting structure of the main body and the lid.

【符号の説明】[Explanation of symbols]

1 本体部 2 蓋部 3 底部壁 4 側壁 6 切欠き 7、9 溝 8、10 凸部 11 シリコーンゴム層 12 出張り DESCRIPTION OF SYMBOLS 1 Main body part 2 Lid part 3 Bottom wall 4 Side wall 6 Notch 7, 9 Groove 8, 10 Convex part 11 Silicone rubber layer 12 Protrusion

Claims (7)

【特許請求の範囲】[Claims] 【請求項1】 培養面となる底部壁とその底部壁を囲む
側壁よりなり、該側壁には開口部となる頚部を有する本
体部と、底部壁と平行に側壁の上端部に嵌合する蓋部と
で構成されるプラスチックの成形品であって、両者の嵌
合部が取り外し可能であるよう仮接着されていることを
特徴とする培養容器。
1. A main body having a bottom wall serving as a culture surface and a side wall surrounding the bottom wall, the main body having a neck serving as an opening in the side wall, and a lid fitted to the upper end of the side wall parallel to the bottom wall. A culture container characterized in that it is a plastic molded article composed of a part and a fitting part of both parts is temporarily adhered so as to be removable.
【請求項2】 本体部と側壁の嵌合部が、側壁上端部の
全周または一部に設けた切欠きまたは溝と、蓋部の周縁
下面の全体または一部に設けた凸部とで形成されている
ことを特徴とする、請求項1記載の培養容器。
2. The fitting portion between the main body portion and the side wall includes a notch or a groove provided on the entire circumference or a part of the upper end portion of the side wall, and a convex portion provided on the whole or a part of the lower peripheral surface of the lid portion. The culture container according to claim 1, wherein the culture container is formed.
【請求項3】 本体部と側壁の嵌合部が、蓋部の周縁下
面の全体または一部に設けた溝に対して、本体部の側壁
上端部または上端部に設けた凸部が嵌合するように形成
してなることを特徴とする、請求項1記載培養容器。
3. The fitting portion between the main body portion and the side wall is fitted with the convex portion provided at the upper end portion or the upper end portion of the side wall of the main body portion with respect to the groove provided on the whole or a part of the lower surface of the peripheral edge of the lid portion. The culture container according to claim 1, wherein the culture container is formed as follows.
【請求項4】 底部壁を囲む側壁の少なくとも一つに沿
って、蓋部の周縁が出張りを形成していることを特徴と
する、請求項1及至請求項3のいずれかに記載の培養容
器。
4. The culture according to any one of claims 1 to 3, wherein the peripheral edge of the lid portion forms a protrusion along at least one of the side walls surrounding the bottom wall. container.
【請求項5】 本体部と蓋部の嵌合部を仮接着するため
の接着剤が液状シリコーンゴムであることを特徴とす
る、請求項1及至請求項4のいずれかに記載の培養容
器。
5. The culture container according to claim 1, wherein the adhesive for temporarily adhering the fitting portion between the main body portion and the lid portion is liquid silicone rubber.
【請求項6】 本体部の側壁上端嵌合部と蓋部の周縁下
面嵌合部のどちらか一方に親水化処理を施したことを特
徴とする、請求項5記載の培養容器。
6. The culture container according to claim 5, wherein one of the side wall upper end fitting portion of the main body portion and the peripheral edge lower surface fitting portion of the lid portion is subjected to a hydrophilic treatment.
【請求項7】 本体部の内面及び側壁上端嵌合部に親水
化処理を施したことを特徴とする、請求項5記載の培養
容器。
7. The culture container according to claim 5, wherein the inner surface of the main body portion and the side wall upper end fitting portion are subjected to a hydrophilic treatment.
JP5020217A 1993-02-08 1993-02-08 Culture vessel Expired - Fee Related JP2740611B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5020217A JP2740611B2 (en) 1993-02-08 1993-02-08 Culture vessel

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Publication Number Publication Date
JPH06233671A true JPH06233671A (en) 1994-08-23
JP2740611B2 JP2740611B2 (en) 1998-04-15

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ID=12021001

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Application Number Title Priority Date Filing Date
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Country Link
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08332071A (en) * 1995-06-06 1996-12-17 Becton Dickinson & Co Assembly of culture slide
JPH08332073A (en) * 1995-06-06 1996-12-17 Becton Dickinson & Co Assembly of culture slide
JPH08332072A (en) * 1995-06-06 1996-12-17 Becton Dickinson & Co Assembly of culture slide
JP2004129558A (en) * 2002-10-10 2004-04-30 Inst Of Physical & Chemical Res Vessel for cell culture, scraper, and method for cell culture
WO2006019836A1 (en) * 2004-07-22 2006-02-23 Corning Incorporated Culture flask
JP2014143998A (en) * 2013-01-18 2014-08-14 Eppendorf Ag Culture bottle
JP2015221002A (en) * 2014-05-22 2015-12-10 大日本印刷株式会社 Cell culture vessel

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JPH04117276A (en) * 1990-09-06 1992-04-17 Sekisui Chem Co Ltd Device for microbe culture medium
JPH0471500U (en) * 1990-11-05 1992-06-24
JPH0497599U (en) * 1991-01-31 1992-08-24
JPH0497600U (en) * 1991-01-31 1992-08-24
JPH04110500U (en) * 1991-03-14 1992-09-25 日本合成ゴム株式会社 Cell culture container

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JPS57192200U (en) * 1981-05-30 1982-12-06
JPS5894383A (en) * 1981-11-30 1983-06-04 Terumo Corp Cover for instrument for cultivation
JPS61146200U (en) * 1985-02-28 1986-09-09
JPS6286900U (en) * 1985-11-22 1987-06-03
JPS62134400U (en) * 1986-02-15 1987-08-24
JPS63173575A (en) * 1987-01-14 1988-07-18 Hitachi Ltd Component for cell manipulating apparatus
JPH04117276A (en) * 1990-09-06 1992-04-17 Sekisui Chem Co Ltd Device for microbe culture medium
JPH0471500U (en) * 1990-11-05 1992-06-24
JPH0497599U (en) * 1991-01-31 1992-08-24
JPH0497600U (en) * 1991-01-31 1992-08-24
JPH04110500U (en) * 1991-03-14 1992-09-25 日本合成ゴム株式会社 Cell culture container

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08332071A (en) * 1995-06-06 1996-12-17 Becton Dickinson & Co Assembly of culture slide
JPH08332073A (en) * 1995-06-06 1996-12-17 Becton Dickinson & Co Assembly of culture slide
JPH08332072A (en) * 1995-06-06 1996-12-17 Becton Dickinson & Co Assembly of culture slide
JP2888332B2 (en) * 1995-06-06 1999-05-10 ベクトン・ディキンソン・アンド・カンパニー Culture slide assembly
JP2891334B2 (en) * 1995-06-06 1999-05-17 ベクトン・ディキンソン・アンド・カンパニー Culture slide assembly
JP2891333B2 (en) * 1995-06-06 1999-05-17 ベクトン・ディキンソン・アンド・カンパニー Culture slide assembly
JP2004129558A (en) * 2002-10-10 2004-04-30 Inst Of Physical & Chemical Res Vessel for cell culture, scraper, and method for cell culture
WO2006019836A1 (en) * 2004-07-22 2006-02-23 Corning Incorporated Culture flask
US7687262B2 (en) 2004-07-22 2010-03-30 Corning Incorporated Flask
JP2014143998A (en) * 2013-01-18 2014-08-14 Eppendorf Ag Culture bottle
JP2015221002A (en) * 2014-05-22 2015-12-10 大日本印刷株式会社 Cell culture vessel

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