JPS5916215B2 - How to transport a support piece for electrophoresis - Google Patents

How to transport a support piece for electrophoresis

Info

Publication number
JPS5916215B2
JPS5916215B2 JP57013315A JP1331582A JPS5916215B2 JP S5916215 B2 JPS5916215 B2 JP S5916215B2 JP 57013315 A JP57013315 A JP 57013315A JP 1331582 A JP1331582 A JP 1331582A JP S5916215 B2 JPS5916215 B2 JP S5916215B2
Authority
JP
Japan
Prior art keywords
support piece
decolorizing
section
liquid
electrophoresis
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.)
Expired
Application number
JP57013315A
Other languages
Japanese (ja)
Other versions
JPS57146143A (en
Inventor
喜代三 越石
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.)
Olympus Corp
Original Assignee
Olympus Optical 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 Olympus Optical Co Ltd filed Critical Olympus Optical Co Ltd
Priority to JP57013315A priority Critical patent/JPS5916215B2/en
Publication of JPS57146143A publication Critical patent/JPS57146143A/en
Publication of JPS5916215B2 publication Critical patent/JPS5916215B2/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/447Systems using electrophoresis
    • G01N27/44704Details; Accessories

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)

Description

【発明の詳細な説明】 本発明は濾紙、セルロースアセテートフィルム等の電気
泳動用支持体片を染色および脱色区間を経て搬送する方
法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for conveying a piece of electrophoretic support, such as a filter paper or a cellulose acetate film, through a dyeing and decolorizing section.

電気泳動法は血清等の体液の蚕白成分の分離定量法とし
て臨床検査の分野で盛んに用いられてい; る方法であ
る。
Electrophoresis is a method that is widely used in the field of clinical testing as a method for separating and quantifying silkworm white components in body fluids such as serum.

分析のプロセスは、濾紙、セルロースアセテートフィル
ム等の支持体片に塗布された血清を泳動分離させ、次い
で支持体片上で分離された成分を染色し、更に支持体片
の血清成分以外の部分を脱色し、その後各成分の光学的
密度を0 濃度計で定量測定するという順序で行なわれ
る。このような分析プロセスに対して電気泳動学会では
標準操作法を制定している。従来このような電気泳動法
による分析は総て人手で行なつている。
The analysis process involves electrophoretically separating the serum applied to a piece of support such as filter paper or cellulose acetate film, then staining the separated components on the support piece, and then decolorizing the parts of the support piece other than the serum components. After that, the optical density of each component is quantitatively measured using a zero densitometer. The Electrophoretic Society has established standard operating methods for such analytical processes. Conventionally, all analyzes using electrophoresis have been performed manually.

すなわち、血清を泳動分離さ5 せた支持体片を染色液
中に浸して染色し、次いで脱色液中に浸して分離成分以
外の部分を脱色するプロセスを人手で行なつている。し
かし、電気泳動法が広く用いられるようになつてくるの
に伴なつて検体数が増大し、特に研究所、大病院では一
’0 田こ非常に多くの検体の定量測定を行なう必要が
生じてきた。このために、人員の確保が必要となると共
に比較的単純な操作を多数回繰返すことによる人的誤差
が生ずる可能性が生じてきた。従つて、上述した分析操
作を自動的に行なう自動染色i5処理装置が望まれるよ
うになつた。このような自動染色処理装置を開発するに
当つては、支持体片を染色区間および脱色区間を経て搬
送する必要が生じたが、支持体片は、例えばセルロース
アセテートフィルムで造られているので、■0 これを
ローラ間に挾んで搬送すると搬送ローラヘの巻き付き等
が生じ支持体片が折れたり、搬送路の途中で詰つたりす
る欠点がある。
That is, the support piece on which the serum has been electrophoretically separated is immersed in a staining solution for staining, and then immersed in a decolorizing solution to decolorize parts other than the separated components, which is manually performed. However, as electrophoresis has become widely used, the number of specimens has increased, and it has become necessary for laboratories and large hospitals in particular to quantitatively measure a large number of specimens. It's here. For this reason, it is necessary to secure personnel, and there is a possibility that human error may occur due to repeating a relatively simple operation many times. Therefore, an automatic staining i5 processing apparatus that automatically performs the above-mentioned analysis operations has become desirable. In developing such an automatic dyeing processing device, it became necessary to transport the support piece through a dyeing section and a decolorizing section, but since the support piece is made of, for example, cellulose acetate film, (20) If this is conveyed while being sandwiched between rollers, it may wind around the conveyance rollers, causing the support piece to break or become clogged in the middle of the conveyance path.

また、支持体片を搬送する場合、フィルムが搬送機構や
その他の部分と接触すると、フィルムに傷がついたり、
■5 汚れが付着したりする欠点がある。このような不
具合が生じないようにするためには、きわめて複雑で高
価な搬送機構が必要となる欠点がある。本発明の目的は
、上述した欠点を解消し、支持体片を染色区間および脱
色区間を経て安定かつ正確に搬送することができ、しか
も任意の搬送機構を用いることができ、さらに搬送中に
フイルムが損傷したり汚れたりすることがないような支
持体片搬送方法を提供しようとするものである。本発明
は、電気泳動法により成分を分離させた支持体片を染色
区間および脱色区間を経て搬送するに当たり、フイルム
状細条の少なく共側縁に枠を取り付けた支持体片の前記
枠と協働する搬送機構によつて支持体片を染色区間およ
び脱色区間を経て搬送することを特徴とするものである
。さらに本発明は、前記フイルム状細条の互いに対向す
る少なく共一対の側縁を溝にはさみ込むように枠を取り
付け、この枠を搬送機構と協働させることを特徴とする
ものである。次に図面を参照して本発明を詳細に説明す
る。
Also, when transporting the support piece, if the film comes into contact with the transport mechanism or other parts, the film may be scratched or
■5 There is a drawback that dirt may adhere. In order to prevent such problems from occurring, a very complicated and expensive transport mechanism is required. An object of the present invention is to eliminate the above-mentioned drawbacks, to be able to transport a support piece stably and accurately through a dyeing section and a decolorizing section, to be able to use an arbitrary transport mechanism, and to prevent film transfer during transport. It is an object of the present invention to provide a method for transporting a support piece in which the support piece is not damaged or soiled. In the present invention, when transporting a support piece whose components have been separated by an electrophoretic method through a dyeing section and a decolorizing section, the present invention provides cooperation with the frame of a support piece that has fewer film-like stripes and has a frame attached to the colateral edge. The present invention is characterized in that the support piece is conveyed through a dyeing section and a decolorizing section by means of a working conveyance mechanism. Furthermore, the present invention is characterized in that a frame is attached so as to sandwich at least a pair of mutually opposing side edges of the film-like strip into the groove, and this frame is made to cooperate with a conveying mechanism. Next, the present invention will be explained in detail with reference to the drawings.

第1図は本発明の支持体片を用い、本発明の搬送方法で
搬送するようにした自動染色処理装置の一例の構成を線
図的に示すものである。本例では、支持体片1を、電気
泳動法の中で現在最も広く用いられているセルロースア
セテートフイルムとする。第1図に示すように、電気泳
動分離された支持体片1を多数収納し、かつ順次に1個
づつ送り出すことができる供給ラツク2を設ける。各支
持体片1は第2図に示すように、セルロースアセテート
フイルムの細条1aの両側縁にプラスチツク枠1b,1
cを取り付けた構造とする。このようにフイルム状細条
1aの側縁に枠1b,1cを設けることにより支持体片
の取扱いは非常に容易となり、後述するように簡単な搬
送機構によつて正確に搬送できる。供給ラツク2の近傍
に連続的に移動する無終端チエーン3を設ける。
FIG. 1 diagrammatically shows the structure of an example of an automatic dyeing processing apparatus that uses the support piece of the present invention and transports it by the transport method of the present invention. In this example, the support piece 1 is a cellulose acetate film, which is currently most widely used in electrophoresis. As shown in FIG. 1, a supply rack 2 is provided which can house a large number of electrophoretically separated support pieces 1 and sequentially feed them out one by one. As shown in FIG.
The structure is such that c is attached. By providing the frames 1b and 1c on the side edges of the film-like strip 1a in this manner, the support pieces can be handled very easily, and can be accurately transported using a simple transport mechanism as will be described later. A continuously moving endless chain 3 is provided in the vicinity of the supply rack 2.

供給ラツク2から送り出される順次の支持体片1はこの
チエーン3の各区画内に装填され、支持体片の枠1b,
1cとチエーン3との協働によりプレート4上を順次に
矢印で示すように右方に送られる。このプレート4は第
3図に示すように両側縁4a,4bを僅かに突出させた
浅い樋状とする。従つて順次の支持体片1の枠1b,1
cがこのプレート4の突縁4a,4b上に乗つて案内さ
れることになる。プレート4は染色区間Sと、脱色区間
Dとを有している。
The successive support pieces 1 delivered from the supply rack 2 are loaded into each section of this chain 3, and the support piece frames 1b,
By the cooperation of 1c and chain 3, it is sequentially sent to the right on plate 4 as shown by the arrow. As shown in FIG. 3, this plate 4 has a shallow gutter shape with both side edges 4a and 4b slightly protruding. Therefore frames 1b, 1 of successive carrier pieces 1
c will be guided by riding on the projecting edges 4a, 4b of this plate 4. The plate 4 has a dyeing section S and a decolorizing section D.

第3図はプレート4の染色区間Sを示し、この区間Sに
おいてプレート4には染色液注入孔S1と、染色液流出
孔S/とを形成する。
FIG. 3 shows a staining section S of the plate 4, and in this section S, the plate 4 is formed with a staining solution injection hole S1 and a staining solution outflow hole S/.

脱色区間Dにおいても、同様の構造の注入孔と流出孔と
の組を5組Dl,D/;D2,D2′;・・・:D5,
DJ(第1図参照)設ける。第1図に示すように、これ
らを支持体片1の移動方向に順次に配置する。またプレ
ート4の表面には注入孔S1と連通する条溝4cを形成
する。支持体片1が染色液注入孔S1の位置にくると、
弁B1を閉じ、弁B2を開き、ポンプP1を働らかせて
、染色液槽C。
In the decolorization section D, five pairs of injection holes and outflow holes having the same structure are arranged Dl,D/;D2,D2';...:D5,
A DJ (see Figure 1) will be provided. As shown in FIG. 1, these are arranged one after another in the direction of movement of the support piece 1. Furthermore, grooves 4c are formed on the surface of the plate 4 to communicate with the injection holes S1. When the support piece 1 comes to the position of the stain solution injection hole S1,
Close valve B1, open valve B2, operate pump P1, and dye bath C.

内の染色液を一定量吸引する。次に弁B2を閉じ、弁B
,を開いてポンプP1を働かせ、吸引した一定量の染色
液をプレート4の染色液注入孔S1から注入し、条溝4
c内に充満させる。支持体片1とプレート4との間の間
隔は小さいから、注入孔S1から注入された染色液は毛
細管現象で支持体片1とプレート4との間に広がり、支
持体片1の全面に染色液が被着することになる。この染
色液は、その粘性および表面張力によつて、支持体片1
とプレート4との間に保持されたま\支持体片1の移動
に伴なつて移動し、染色液流出孔S/の位置に達する。
支持体片1がS1からS/まで移動する時間を、1分3
0秒〜3分の間の適当な時間に定め、この時間中に規定
の染色処理が行なわれるようにする。
Aspirate a certain amount of the staining solution inside. Then close valve B2 and
, open the pump P1, inject a certain amount of the suctioned staining liquid from the staining liquid injection hole S1 of the plate 4, and fill the groove 4.
Fill in c. Since the distance between the support piece 1 and the plate 4 is small, the staining solution injected from the injection hole S1 spreads between the support piece 1 and the plate 4 due to capillary action, staining the entire surface of the support piece 1. The liquid will adhere to it. Due to its viscosity and surface tension, this staining solution is applied to the support piece 1.
While being held between the support piece 1 and the plate 4, it moves as the support piece 1 moves and reaches the position of the staining solution outflow hole S/.
The time it takes for support piece 1 to move from S1 to S/ is 1 minute 3
A suitable time between 0 seconds and 3 minutes is set, and the specified dyeing process is performed during this time.

流出孔S/の位置に達すると染色液は流出孔S/を経て
流下し、染色液槽C。中に戻る。このようにして染色液
は循環しながら、順次の支持体片1を染色することにな
る。このように同一の染色液を多数の支持体片の染色に
使用することができるので、染色液の使用量は少なくて
済み、染色液槽COを、容積の小さいものとすることが
できると共に処理コストを下げることができる。染色液
としては、ホンソー3Rを6%のトリクロル酢酸水溶液
に0.4〜0.8%に溶解したものを用いる。プレート
4の脱色区間Dでは脱色操作が行なわれ、支持体片上に
分離された血清成分以外の部分は脱色される。本例装置
では、5個の脱色液槽C1〜C5を設け、これら液槽中
の脱色液を1台のポンプP2によつて吸排し、順次の脱
色位置で順次の支持体片1に脱色液を被着し得るように
する。すなわち、或る支持体片1に注目した場合、これ
が第1の脱色液注入孔D,の位置にあるとき、弁E2を
開いてポンプP2を作動させ、第1の脱色液槽C1から
一定量の脱色液を吸引する。この場合)他の弁El9f
l9f29glツG29hlツH2!11,i2は総て
閉じている。次に弁e1を開き、弁E2を閉じてポンプ
P2を駆動し、脱色注入孔D1から脱色液を注入する。
注入後弁e1を閉じる。上述した染色区間Sにおけるの
と同様に、脱色液は毛細管現象により支持体片1とプレ
ート4との間に充満し、更に支持体片1と一緒に脱色液
流出孔D/の位置まで移動し、ここから流出する。この
流出される脱色液は染色液により著しく汚染されている
から廃棄する。この支持体片1が第2の脱色液注入孔D
2の位置に来ると、弁F2を開き、ポンプP2を再び駆
動し、脱色液槽C2から一定量の脱色液を吸引する。次
に弁F2を閉じ、弁f1を開いて吸引した脱色液を第2
脱色液注入孔D2を経て支持体片1とプレート4との間
に注入する。注入後弁f1を閉じる。支持体片1が第2
の脱色液流出孔Dダの位置に来ると、支持体片1とプレ
ート4との間に保持した脱色液を流出孔D2′を経て流
出させる。この脱色液は第1の脱色液槽C1に戻す。以
下、支持体片1が第3,第4,第5の脱色液注入孔D3
,D4,D5の位置に来たときに第3,第4,第5の脱
色液槽C3,C4,C5から脱色液を注入し、第3,第
4,第5の流出孔Df,D4′,Dlを経て流出させ、
第2,第3,第4の脱色液槽C2,C3,C4に戻す。
第5の脱色液槽C5には新たな脱色液を補給するように
する。このように構成することにより、順次の脱色液槽
C1〜C5には染色液で汚染される程度の少ない脱色液
が収容されているため、きわめて少量の脱色液で理想的
な脱色操作が行なわれる。脱色液としては、1〜3%の
酢酸水溶液を用いる。
When the staining liquid reaches the position of the outflow hole S/, it flows down through the outflow hole S/ and enters the staining liquid tank C. Go back inside. In this way, the dyeing solution is circulated and dyes successive pieces of support 1. In this way, the same staining liquid can be used for staining a large number of support pieces, so the amount of staining liquid used can be reduced, and the volume of the staining liquid bath CO can be reduced, and the processing time can be reduced. Costs can be lowered. As the staining solution, 0.4 to 0.8% of Honso 3R dissolved in a 6% trichloroacetic acid aqueous solution is used. In the decolorization section D of the plate 4, a decolorization operation is performed, and parts other than the serum components separated on the support piece are decolorized. In the apparatus of this example, five decolorizing liquid tanks C1 to C5 are provided, and the decolorizing liquid in these liquid tanks is sucked and discharged by one pump P2, and the decolorizing liquid is applied to the support pieces 1 at successive decolorizing positions. be able to be coated. That is, when focusing on a certain support piece 1, when it is at the position of the first decolorizing liquid injection hole D, the valve E2 is opened and the pump P2 is operated, and a certain amount is poured from the first decolorizing liquid tank C1. Aspirate the decolorizing solution. In this case) other valve El9f
19f29gl, G29hl, H2!11, i2 are all closed. Next, the valve e1 is opened, the valve E2 is closed, the pump P2 is driven, and the decolorizing liquid is injected from the decolorizing injection hole D1.
After injection, close valve e1. As in the staining section S described above, the decolorizing liquid fills between the support piece 1 and the plate 4 due to capillary action, and further moves together with the support piece 1 to the position of the decolorizing liquid outflow hole D/. , flows from here. This drained decolorizing solution is heavily contaminated with the staining solution and is therefore discarded. This support piece 1 is connected to the second decolorizing liquid injection hole D.
When reaching position 2, the valve F2 is opened, the pump P2 is driven again, and a certain amount of decolorizing liquid is sucked from the decolorizing liquid tank C2. Next, close the valve F2, open the valve f1, and transfer the suctioned decolorizing liquid to the second
The decolorizing liquid is injected between the support piece 1 and the plate 4 through the injection hole D2. After injection, close valve f1. Support piece 1 is the second
When reaching the position of the decolorizing liquid outflow hole D, the decolorizing liquid held between the support piece 1 and the plate 4 is caused to flow out through the outflow hole D2'. This decolorizing liquid is returned to the first decolorizing liquid tank C1. Hereinafter, the support piece 1 is connected to the third, fourth, and fifth decolorizing liquid injection holes D3.
, D4, and D5, the decolorizing liquid is injected from the third, fourth, and fifth decolorizing liquid tanks C3, C4, and C5, and the decolorizing liquid is injected into the third, fourth, and fifth outflow holes Df, D4'. , Flow out through Dl,
It is returned to the second, third, and fourth decolorizing liquid tanks C2, C3, and C4.
A new decolorizing liquid is supplied to the fifth decolorizing liquid tank C5. With this configuration, the sequential decolorizing liquid tanks C1 to C5 contain decolorizing liquid that is less likely to be contaminated with the staining liquid, so that an ideal decolorizing operation can be performed with an extremely small amount of decolorizing liquid. . A 1 to 3% acetic acid aqueous solution is used as the decolorizing solution.

また支持体片1がD1からD/,D2からDI・・・D
5からD冫まで移動する時間が1〜2分となるようにす
る。第1図の区間Kは加熱区間であり、ヒーター5によ
り加熱した空気を支持体片1に送り、乾燥する。
Also, the support piece 1 is D1 to D/, D2 to DI...D
The time it takes to move from 5 to D is 1 to 2 minutes. Section K in FIG. 1 is a heating section, in which air heated by heater 5 is sent to support piece 1 to dry it.

このようにして、染色、脱色、乾燥処理の終つた支持体
片1はプレート4の右端でプレート4から落下し、収納
ラツク6内に収納される。第1図において、染色液槽C
。内に収容された染色液はその量が徐々に減少すると共
に染色効果が低下する。従つて、例えばカウンターによ
つて検体数をカウントし、所定の検体数たけ処理した後
に、染色液を補給するか交替する必要がある。また第5
の脱色液槽C5内の脱色液も処理が進むにつれて減少す
るから、所定の検体数だけ処理した後に脱色液を補給す
るか交替する必要がある。第1図においては、符号7で
示すプロツクがこのような機能を有するものである。第
4図は1台のポンプP2によつて脱色液の注入を行なう
場合、同時刻に弁の動作が重ならないようにするための
タイミングを示す線図である。
In this way, the support piece 1 that has been dyed, bleached, and dried falls off the right end of the plate 4 and is stored in the storage rack 6. In Figure 1, staining solution tank C
. As the amount of the dyeing liquid stored in the container gradually decreases, the dyeing effect also decreases. Therefore, it is necessary to count the number of specimens using a counter, for example, and to replenish or replace the staining solution after processing a predetermined number of specimens. Also the fifth
Since the decolorizing liquid in the decolorizing liquid tank C5 also decreases as the processing progresses, it is necessary to replenish or replace the decolorizing liquid after processing a predetermined number of samples. In FIG. 1, a block designated by the reference numeral 7 has such a function. FIG. 4 is a diagram showing the timing to avoid overlapping valve operations at the same time when the decolorizing liquid is injected by one pump P2.

順次の支持体片1の移送間隔をPとし、順次の脱色液注
入孔と流出孔との間隔DlD/−D2D2′D3Df−
D4D4′−D5D♂−Pとし、順次の脱色液注入孔の
間隔をDlD2−11,D2D3−.(!2,D3D4
−13,D4D5−14とするとき、のような位置関係
をもたせることによつて弁が同時に開くことを阻止する
ことができる。ここにM,nは正数であつて、mは支持
体片1の移動速度、装置の寸法等の設計要素によつて適
当な値に選定され、nは脱色液注入孔の個数によつて定
められる。電気泳動学会によつて制定された標準操作法
によれば、脱色液を5回変える方法が推奨されているの
で、その場合には、n−5とすればよい。第1図および
第4図はn−5の例であり、支持体片群が右方へ移送さ
れるものであり、支持体片11に脱色液が注入された後
、支持体片群が−P) 5たけ右方
へ移動すると、支持体片1−2に脱色液が注入される。
The interval between successive transfers of the support pieces 1 is P, and the interval between the successive decolorizing liquid injection holes and outflow holes DlD/-D2D2'D3Df-
D4D4'-D5D♂-P, and the intervals between the sequential decolorizing liquid injection holes are D1D2-11, D2D3-. (!2, D3D4
-13, D4D5-14, it is possible to prevent the valves from opening at the same time by providing the following positional relationship. Here, M and n are positive numbers, m is selected to an appropriate value depending on design factors such as the moving speed of the support piece 1 and the dimensions of the device, and n is selected depending on the number of decolorizing liquid injection holes. determined. According to the standard operating method established by the Electrophoretic Society, it is recommended to change the decolorizing solution five times, so in that case, n-5 may be used. 1 and 4 are examples of n-5, in which the support piece group is transferred to the right, and after the decolorizing liquid is injected into the support piece 11, the support piece group is transferred to the - P) When moving 5 degrees to the right, the decolorizing liquid is injected into the support piece 1-2.

更に−Pたけ移動して支持体片1−3に脱色液が注入さ
れる。
The decolorizing liquid is further moved by -P and is injected into the support piece 1-3.

以下、支持体片が−Pたけ移動す0 ゝ
5る毎に支持体片1−3,1−4,1−5に脱色
液が注入される。
Below, the support piece moves by -P 0ゝ
A decolorizing liquid is injected into the support pieces 1-3, 1-4, and 1-5 every 5 minutes.

更に−Pたけ移動すると、脱色液*注入孔D1の位置に
来る支持体片1−1 に脱色液が注入され、以下−Pた
け移動する毎に支持体片1−28,1−38,1−48
,1−58に脱色液が注入される。
When the support piece 1-1 moves further by -P, the decolorizing liquid is injected into the support piece 1-1 that comes to the position of the decolorizing liquid* injection hole D1, and thereafter, every time the support piece 1-2 moves by -P, the support piece 1-28, 1-38, 1 -48
, 1-58, the decolorizing solution is injected.

このように脱色液の注入タイミングをずらすことにより
、1台の比較的小型のポンプを用いることができ、この
場合、脱色液間の混合も起らない。これに対し総ての脱
色液の注入を1台のポンプにより同時に行なうとすると
大型のポンプが必要になると共に脱色液の混合が起る惧
れが上述したように、本発明によればフイルム状細条の
側縁に枠を取り付けて支持体片を構成することによりそ
の搬送は非常に簡単かつ正確となると共に搬送機構とし
てもベルト、チエーン等任意の搬送機構を用いることが
できる。また、フイルム状細条の側縁を溝にはさみ込む
ようにして枠を取り付ける場合には、フイルム状細条に
多少のたるみがあつても、フイルム状細条が搬送機構や
他の部分に接触することがないので、フイルム状細条に
傷や汚れが付くことがなくなる。本発明は上述した例に
のみ限定されるものではなく、幾多の変更を加え得るこ
と勿論である。
By shifting the injection timing of the decolorizing liquid in this manner, one relatively small pump can be used, and in this case, mixing between the decolorizing liquids does not occur. On the other hand, if all the decolorizing liquids were to be injected at the same time using one pump, a large pump would be required and there would be a risk of mixing of the decolorizing liquids. By attaching a frame to the side edge of the strip to form a support piece, its conveyance becomes very simple and accurate, and any conveyance mechanism such as a belt or chain can be used as the conveyance mechanism. In addition, when attaching the frame so that the side edges of the film-like strips are inserted into the grooves, even if the film-like strips have some slack, the film-like strips will not come into contact with the conveyance mechanism or other parts. Since there are no scratches or stains on the film-like strips, there is no possibility of scratches or stains on the film-like strips. It goes without saying that the present invention is not limited to the above-mentioned examples, but can be modified in many ways.

例えば上述した例ではチエーン3を用いたが、ベルトそ
の他の適当な移送機構を用いることもできる。またチエ
ーン、ベルト等は必らずしも連続的に送る必要はなく、
間欠的に送ることもできる。また、上述の例では、染色
処理した支持体片1を収納ラツク6に落し込むようにし
たが、順次の染色処理した支持体片1を濃度計に直接送
り込んで光学的密度を測定して定量分析するようにする
こともできる。この場合には電気泳動法による分析定量
を行なう自動測定装置が得られる。更に上述した例では
1台のポンプによつて5回の脱色液注入を行なうように
したが、例えば5個のポンプを設けることもできる。こ
の場合にはこれら5個のポンプを同時に駆動することが
できる。また染色液、脱色液注人、流出機構も土述した
例たけに限定されるものではなく、他の任意の注入、流
出機構を用いることができる。また上述した例では支持
体片1には1検体分のフイルム1aを収納したが複数の
検体のフイルムを同時に収納することもできる。またフ
イルム1aは上述したように枠1b,1cで両側縁のみ
を挾んだ構造とする必要はなく、前、後縁も枠で挾むこ
ともでき、プラスチツクケース内に収納することもでき
る。
For example, although a chain 3 is used in the example described above, a belt or other suitable transport mechanism may also be used. Also, chains, belts, etc. do not necessarily need to be fed continuously.
It can also be sent intermittently. Further, in the above example, the dyed support piece 1 is dropped into the storage rack 6, but the dyed support piece 1 is successively fed directly into the densitometer to measure the optical density for quantitative determination. It can also be analyzed. In this case, an automatic measuring device is obtained that performs analytical quantification by electrophoresis. Further, in the above example, one pump is used to inject the decolorizing liquid five times, but for example, five pumps may be provided. In this case, these five pumps can be driven simultaneously. Furthermore, the dyeing liquid, decolorizing liquid pourer, and outflow mechanism are not limited to the above-mentioned examples, and any other arbitrary injection and outflow mechanism may be used. Further, in the above-mentioned example, the film 1a for one specimen is stored in the support piece 1, but it is also possible to store the films for a plurality of specimens at the same time. Further, the film 1a does not need to have a structure in which only the opposite edges are held between the frames 1b and 1c as described above, but the front and rear edges can also be held between the frames, and the film 1a can also be stored in a plastic case.

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

第1図は本発明の支持体片搬送方法を適用した自動染色
処理装置の一例の構成を示す線図、第2図は第1図に示
す自動染色処理装置に用いる本発明の支持体片の一例の
構成を示す斜視図、第3図は第1図に示す自動染色処理
装置のプレートの構造を示す斜視図、第4図は第1図に
示す自動染色処理装置における脱色操作を示す線図であ
る。 1・・・・・・支持体片、1a・・・・・・フイルム状
細条、1b,1c・・・・・・枠、2・・・・・・供給
ラツク、3・・・・・・無終端チエーン、4・・・・・
・プレート、5・・・・・・ヒーター6・・・・・・収
納ラツタ、S・・・・・・染色区間、D・・・・・・脱
色区間、K・・・・・・乾燥区間、P1・・・・・・染
色液供給ポンプ、P2......脱色液供給ポンプ、
CO・・・・・・染色液槽、C1〜C5・・・・・・脱
色液槽。
FIG. 1 is a diagram showing the configuration of an example of an automatic staining processing apparatus to which the support piece conveying method of the present invention is applied, and FIG. FIG. 3 is a perspective view showing the structure of the plate of the automatic staining processing device shown in FIG. 1; FIG. 4 is a diagram showing the decoloring operation in the automatic staining processing device shown in FIG. 1. It is. 1... Support piece, 1a... Film strip, 1b, 1c... Frame, 2... Supply rack, 3...・Endless chain, 4...
・Plate, 5...Heater 6...Storage rack, S...Dyeing section, D...Decolorizing section, K...Drying section , P1... Staining solution supply pump, P2. .. .. .. .. .. decolorizing liquid supply pump,
CO...Staining solution tank, C1-C5...Decolorization solution tank.

Claims (1)

【特許請求の範囲】 1 電気泳動法により成分を分離させた支持体片を染色
区間および脱色区間を経て搬送するに当たり、フィルム
状細条の少なく共側縁に枠を取り付けた支持体片の前記
枠と協働する搬送機構によつて支持体片を染色区間およ
び脱色区間を経て搬送することを特徴とする電気泳動用
支持体片の搬送方法。 2 前記支持体片を複数個収納する収納部から支持体片
を順次に送り出し、染色区間および脱色区間を経て搬送
した後格納部へ格納することを特徴とする特許請求の範
囲第1項記載の電気泳動用支持体片の搬送方法。 3 前記フィルム状細条の互いに対向する少なく共一対
の側縁を溝にはさみ込むように枠を取り付け、この枠を
搬送機構と協動させることを特徴とする特許請求の範囲
第1項記載の電気泳動用支持体片の搬送方法。
[Scope of Claims] 1. When transporting a support piece whose components have been separated by electrophoresis through a dyeing section and a decolorizing section, the above-mentioned support piece having fewer film-like stripes and a frame attached to the colateral edge is used. A method for transporting a support piece for electrophoresis, characterized in that the support piece is transported through a dyeing section and a decolorizing section by a transport mechanism that cooperates with a frame. 2. The method according to claim 1, characterized in that the support pieces are sequentially sent out from a storage unit that stores a plurality of the support pieces, and are stored in the storage unit after being transported through a dyeing section and a decolorizing section. A method of transporting a support piece for electrophoresis. 3. A frame according to claim 1, characterized in that a frame is attached so that at least a pair of mutually opposing side edges of the film-like strip are sandwiched in the groove, and this frame is made to cooperate with a conveyance mechanism. A method of transporting a support piece for electrophoresis.
JP57013315A 1982-02-01 1982-02-01 How to transport a support piece for electrophoresis Expired JPS5916215B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57013315A JPS5916215B2 (en) 1982-02-01 1982-02-01 How to transport a support piece for electrophoresis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57013315A JPS5916215B2 (en) 1982-02-01 1982-02-01 How to transport a support piece for electrophoresis

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP48021779A Division JPS5810695B2 (en) 1973-02-24 1973-02-24 Automatic staining processing method

Publications (2)

Publication Number Publication Date
JPS57146143A JPS57146143A (en) 1982-09-09
JPS5916215B2 true JPS5916215B2 (en) 1984-04-13

Family

ID=11829734

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57013315A Expired JPS5916215B2 (en) 1982-02-01 1982-02-01 How to transport a support piece for electrophoresis

Country Status (1)

Country Link
JP (1) JPS5916215B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4812216A (en) * 1987-08-28 1989-03-14 Bios Corporation Method of handling and transporting a transfer membrane used in a blotting apparatus

Also Published As

Publication number Publication date
JPS57146143A (en) 1982-09-09

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