JPH0535328Y2 - - Google Patents
Info
- Publication number
- JPH0535328Y2 JPH0535328Y2 JP17252187U JP17252187U JPH0535328Y2 JP H0535328 Y2 JPH0535328 Y2 JP H0535328Y2 JP 17252187 U JP17252187 U JP 17252187U JP 17252187 U JP17252187 U JP 17252187U JP H0535328 Y2 JPH0535328 Y2 JP H0535328Y2
- Authority
- JP
- Japan
- Prior art keywords
- sample
- electrode
- container
- containers
- 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 - Lifetime
Links
- 238000001962 electrophoresis Methods 0.000 claims description 20
- 238000000926 separation method Methods 0.000 claims description 20
- 239000008151 electrolyte solution Substances 0.000 claims description 17
- 238000005192 partition Methods 0.000 claims description 7
- 230000002378 acidificating effect Effects 0.000 claims description 4
- 229940021013 electrolyte solution Drugs 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000012670 alkaline solution Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000003929 acidic solution Substances 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 1
- 230000005520 electrodynamics Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
Landscapes
- Peptides Or Proteins (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
Description
【考案の詳細な説明】
〔産業上の利用分野〕
この考案は電気泳動で用いられる電気泳動装置
に関する。[Detailed Description of the Invention] [Industrial Application Field] This invention relates to an electrophoresis device used in electrophoresis.
電気永動は、電解質溶液を入れた二つの容器を
分離用ゲルで連結し、一方の容器内に分析用試料
(各種のタンパク質等)を導入し、前記二つの電
解質溶液に電極を挿入して直流電圧をかけ、試料
微粒子を帯電且つ泳動させこの微粒子の成分を分
析する方法である。
Electrodynamics involves connecting two containers containing electrolyte solutions with a separation gel, introducing a sample for analysis (various proteins, etc.) into one container, and inserting electrodes into the two electrolyte solutions. In this method, a direct current voltage is applied to charge and migrate sample particles, and the components of these particles are analyzed.
上記する電気泳動で用いられる従来の電気泳動
装置は第3図に示すような構造になつている。即
ち、一方にはアルカリ性溶液(例えば水酸化ナト
リウム溶液)を入れた容器Aを、他方には酸性溶
液(例えばリン酸溶液)を入れた容器Bを置き、
これらの容器間を分離用ゲルCで連結し、このゲ
ルCに多孔質フイルタDを介して電解液が接触す
る構造になつている。そして前記アルカリ性溶液
を入れた容器Aにはマイクロシリンジ等で試料E
を導入し、直流電圧をかけ帯電した試料Eを分離
用ゲルCに滲出させて電気泳動させ、分析するよ
うになつている。 The conventional electrophoresis apparatus used in the above electrophoresis has a structure as shown in FIG. That is, a container A containing an alkaline solution (e.g., sodium hydroxide solution) is placed on one side, and a container B containing an acidic solution (e.g., a phosphoric acid solution) is placed on the other side.
These containers are connected by a separation gel C, and the electrolyte is in contact with the gel C via a porous filter D. Then, sample E is added to container A containing the alkaline solution using a microsyringe or the like.
is introduced, a DC voltage is applied, the charged sample E is oozed into a separation gel C, electrophoresed, and analyzed.
上記するような従来の電気泳動装置では、分離
用ゲルと容器中の試料とがフイルタを介して常に
接触するようになつている。従つて、全泳動時間
にわたつて分離用ゲルと試料とが接触しているの
でしばしば分析結果にテーリングが生じていた
り、短時間で効率良く分離出来ないという問題が
あつた。また、現在実施されている上記装置では
一度サンプリングするとゲルと試料とを完全に分
離出来なくなるという問題があつた。
In the conventional electrophoresis apparatus as described above, the separation gel and the sample in the container are always in contact with each other via a filter. Therefore, since the separation gel and the sample are in contact for the entire electrophoresis time, there are problems in that tailing often occurs in the analysis results and that efficient separation cannot be performed in a short time. Furthermore, the above-mentioned apparatus currently in use has a problem in that once sampling is performed, the gel and sample cannot be completely separated.
この考案はかかる問題点に鑑みてなされたもの
であり、その目的とするところは任意の時点で分
離用ゲルと試料とを分離出来るようにし上記問題
点を解決することにある。 This invention was made in view of the above problems, and its purpose is to solve the above problems by making it possible to separate the separation gel and the sample at any time.
即ち、この考案は上記する問題点を解決するた
めに、一方にはアルカリの電解溶液を他方には酸
性の電解溶液を入れる二つの容器と、これらの容
器を連結する分離用ゲルと、前記二つの容器の電
解溶液にそれぞれ陰極と陽極とを入れた直流電源
とよりなる電気泳動装置において、前記一方の容
器を隔壁により複数個の部屋に分離してその一つ
を試料用部屋とし、該複数個に分離した各部屋に
同一電極内で切り換え可能な電極を入れたことを
特徴とする。
That is, in order to solve the above-mentioned problems, this invention consists of two containers, one containing an alkaline electrolytic solution and the other containing an acidic electrolytic solution, a separation gel connecting these containers, and a separation gel that connects these containers. In an electrophoresis apparatus consisting of a DC power supply with a cathode and an anode placed in electrolytic solutions in two containers, one of the containers is separated into a plurality of chambers by a partition wall, one of which is used as a sample chamber, and the plurality of It is characterized by having switchable electrodes within the same electrode placed in each separate room.
初めに試料を入れた部屋の電極に直流電圧をか
けると、試料は帯電して分離用ゲルに滲出してい
く。次に、適当な時期に試料の入つていない部屋
の電極に切り換えると試料は電気の流れの外に置
かれ容器内の試料は分離用ゲルには入らなくな
る。従つて、分離用ゲル内での以降の電気泳動で
は容器内の試料とは切り離して電気泳動を行わせ
ることが出来る。
When a direct current voltage is applied to the electrodes in the chamber containing the sample, the sample becomes electrically charged and oozes into the separation gel. Next, at an appropriate time, the electrodes are switched to a room that does not contain a sample, and the sample is placed outside the current of electricity and the sample in the container no longer enters the separation gel. Therefore, subsequent electrophoresis within the separation gel can be performed separately from the sample in the container.
以下、この考案の具体的実施例について図面を
参照して説明する。
Hereinafter, specific embodiments of this invention will be described with reference to the drawings.
第1図はこの考案にかかる電気泳動装置の試料
を導入する容器側の縦断側図である。この図で1
は電解質溶液を入れた容器、2はこの容器1に入
れた電解質溶液であり、例えば水酸化ナトリウム
のアルカリ溶液が入れてある。3は電極(−極)、
3′は同じく電極(−極)であつて、回転接触子
30により電極3の端子31或いは電極3′の端
子32のいずれかに任意に切換え可能となつてい
る。4はこの容器1を二つの部屋12と13に仕
切るための隔壁であるが、この図で示すように部
屋13はクランク状或いはラビリンス状となつて
前記隔壁4の下部で前記部屋12及びフイルタ5
につながつている。6は分離用ゲルでありこのゲ
ル6は例えばポリアクリルアミドで製作される。
7は前記クランク状或いはラビリンス状の部屋1
3の下部にマイクロシリンジ14で導入した分析
試料である。この分析試料としては例えば種々の
タンパク質の混合物などがある。 FIG. 1 is a longitudinal sectional side view of the electrophoresis apparatus according to this invention on the side of a container into which a sample is introduced. In this diagram 1
2 is a container containing an electrolyte solution, and 2 is an electrolyte solution placed in this container 1, which contains, for example, an alkaline solution of sodium hydroxide. 3 is an electrode (-pole),
Reference numeral 3' is also an electrode (-pole), which can be arbitrarily switched to either the terminal 31 of the electrode 3 or the terminal 32 of the electrode 3' by means of a rotary contactor 30. Reference numeral 4 denotes a partition wall for partitioning the container 1 into two chambers 12 and 13. As shown in this figure, the chamber 13 is shaped like a crank or a labyrinth, and the chamber 12 and the filter 5 are separated from each other at the bottom of the partition wall 4.
connected to. 6 is a separation gel, and this gel 6 is made of polyacrylamide, for example.
7 is the crank-shaped or labyrinth-shaped room 1
This is an analysis sample introduced into the lower part of 3 with a microsyringe 14. This analysis sample includes, for example, a mixture of various proteins.
第2図はこの考案にかかる電気泳動装置の全体
概要図である。この図で8は酸性の電解溶液9を
入れた容器であり、この酸性溶液9としては例え
ばリン酸液が入れてある。また、前記容器8の溶
液内には電極(+極)10が入れてあり前記容器
1の電極3或いは3′に電源11を介してつなが
れている。更に前記容器8は分離用ゲル6を介し
て容器1とつながれている。即ち、分離用ゲル6
は一方はアルカリ溶液、他方は酸性溶液として分
離用ゲル6に試料が電気泳動する際の駆動源とし
て直流電圧をかけるようになつている。15は分
離用ゲル6の下に設置した冷却板である。 FIG. 2 is an overall schematic diagram of the electrophoresis apparatus according to this invention. In this figure, 8 is a container containing an acidic electrolytic solution 9, and the acidic solution 9 is, for example, a phosphoric acid solution. Further, an electrode (+ electrode) 10 is placed in the solution in the container 8 and connected to the electrode 3 or 3' of the container 1 via a power source 11. Further, the container 8 is connected to the container 1 via a separation gel 6. That is, the separation gel 6
One is an alkaline solution and the other is an acidic solution, and a DC voltage is applied as a driving source when the sample is electrophoresed on the separation gel 6. 15 is a cooling plate installed under the separation gel 6.
而して、第1図及び第2図に示すように多孔質
フイルタ5を介して電解液2がゲル6に接触して
いることは従来と同じであるが、電解液2を入れ
た容器1の部屋は12と13の二つに分かれてお
り、また試料も部屋13へ導入するようになつて
いる。そして試料を分離用ゲル6に導入するとき
は回転接触子30を前記試料側の部屋13に入れ
た電極3′の端子32に接触させて直流電圧をか
けるのである。こうして直流電流を導通させると
試料は電荷すると共にフイルタ5より出て分離用
ゲル6内を泳動し各タンパク質固有の成分ごとに
分離されて行く。また、適切な時期に回転接触子
30を電極3′から電極3に切り換えると電流は
破線のように流れ、容器中の試料7は電気の流れ
の外に置かれることなり部屋13から出て来るこ
とが出来なくなる。従つて電極3′から3に切り
換えた後の電気泳動では全く試料とは切り離して
泳動させることが出来る。 As shown in FIGS. 1 and 2, the electrolytic solution 2 is in contact with the gel 6 through the porous filter 5 as in the conventional case, but the container 1 containing the electrolytic solution 2 is The room is divided into two, 12 and 13, and the sample is also introduced into room 13. When a sample is introduced into the separating gel 6, the rotary contactor 30 is brought into contact with the terminal 32 of the electrode 3' placed in the chamber 13 on the sample side, and a DC voltage is applied. When a direct current is applied in this manner, the sample becomes electrically charged and exits from the filter 5 and migrates within the separation gel 6, where it is separated into components unique to each protein. Furthermore, when the rotating contactor 30 is switched from electrode 3' to electrode 3 at an appropriate time, the current flows as shown by the broken line, and the sample 7 in the container is placed outside the flow of electricity and comes out of the chamber 13. I can't do anything. Therefore, in electrophoresis after switching from electrode 3' to electrode 3, electrophoresis can be performed completely separately from the sample.
尚、隔壁4により分けた容器1の部屋12と1
3の容量は、部屋12が20ml〜50ml程度で、部屋
13は5ml〜10ml程度とするのが適当である。 Note that the chambers 12 and 1 of the container 1 are separated by a partition wall 4.
It is appropriate that the capacity of room 12 is about 20 ml to 50 ml, and the capacity of room 13 is about 5 ml to 10 ml.
この考案にかかる電気泳動装置は以上詳述した
ような構成としたので、電気永動のある時点以降
全く試料とは分離して泳動出来る。その結果短時
間で効率良くゲル中に試料を導入出来るし、また
テーリングを防止して正確な分析結果を得ること
が出来る。
Since the electrophoresis apparatus according to this invention has the configuration described in detail above, it is possible to perform electrophoresis completely separated from the sample after a certain point in electrophoresis. As a result, the sample can be efficiently introduced into the gel in a short time, and tailing can be prevented and accurate analysis results can be obtained.
第1図はこの考案にかかる電気泳動装置のサン
プリングポート部分の縦断面図、第2図はこの考
案にかかる電気泳動装置の全体概要図、第3図は
従来の電気永動装置の概要図である。
1……電解質溶液用容器、2……電解質溶液
(アルカリ性)、3,3′……電極(−極)、4……
隔壁、5……多孔質フイルタ、6……分離用ゲ
ル、7……試料、8……電解質溶液用容器、9…
…電解質溶液(酸性)、10……電極(+極)、1
1……直流電源、12,13……仕切り部屋、3
0……回転接触子、31,32……端子。
Fig. 1 is a longitudinal sectional view of the sampling port portion of the electrophoresis device according to this invention, Fig. 2 is an overall schematic diagram of the electrophoresis device according to this invention, and Fig. 3 is a schematic diagram of a conventional electrophoresis device. be. 1...Container for electrolyte solution, 2...Electrolyte solution (alkaline), 3,3'...electrode (-electrode), 4...
Partition wall, 5...Porous filter, 6...Separation gel, 7...Sample, 8...Container for electrolyte solution, 9...
... Electrolyte solution (acidic), 10 ... Electrode (+ electrode), 1
1... DC power supply, 12, 13... Partition room, 3
0... Rotating contact, 31, 32... Terminal.
Claims (1)
電解溶液を入れる二つの容器と、これらの容器を
連結する分離用ゲルと、前記二つの容器の電解溶
液にそれぞれ陰極と陽極とを入れた直流電源とよ
りなる電気泳動装置において、前記一方の容器を
隔壁により複数個の部屋に分離してその一つを試
料用部屋とし、該複数個に分離した各部屋に同一
電極内で切り換え可能な電極を入れたことを特徴
とする電気泳動装置。 Two containers containing an alkaline electrolytic solution in one and an acidic electrolytic solution in the other, a separation gel connecting these containers, and a direct current containing a cathode and an anode in the electrolytic solutions in the two containers, respectively. In an electrophoresis apparatus comprising a power source, one of the containers is separated into a plurality of chambers by a partition wall, one of which is used as a sample chamber, and each of the plurality of separated chambers is provided with an electrode that can be switched within the same electrode. An electrophoresis device characterized by containing.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17252187U JPH0535328Y2 (en) | 1987-11-11 | 1987-11-11 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17252187U JPH0535328Y2 (en) | 1987-11-11 | 1987-11-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0177944U JPH0177944U (en) | 1989-05-25 |
| JPH0535328Y2 true JPH0535328Y2 (en) | 1993-09-08 |
Family
ID=31464490
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17252187U Expired - Lifetime JPH0535328Y2 (en) | 1987-11-11 | 1987-11-11 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0535328Y2 (en) |
-
1987
- 1987-11-11 JP JP17252187U patent/JPH0535328Y2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0177944U (en) | 1989-05-25 |
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