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SU552373A1 - Electrophoretic Elution Apparatus - Google Patents

Electrophoretic Elution Apparatus

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Publication number
SU552373A1
SU552373A1 SU2080651A SU2080651A SU552373A1 SU 552373 A1 SU552373 A1 SU 552373A1 SU 2080651 A SU2080651 A SU 2080651A SU 2080651 A SU2080651 A SU 2080651A SU 552373 A1 SU552373 A1 SU 552373A1
Authority
SU
USSR - Soviet Union
Prior art keywords
elution apparatus
electrophoretic elution
cell
compartment
fractions
Prior art date
Application number
SU2080651A
Other languages
Russian (ru)
Inventor
Галина Евгеньевна Цимаркина
Елена Израйлевна Панкратьева
Елена Абрамовна Дыскина
Сергей Иванович Гущин
Original Assignee
Специальное Конструкторское Бюро Биофизической Аппаратуры
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 Специальное Конструкторское Бюро Биофизической Аппаратуры filed Critical Специальное Конструкторское Бюро Биофизической Аппаратуры
Priority to SU2080651A priority Critical patent/SU552373A1/en
Application granted granted Critical
Publication of SU552373A1 publication Critical patent/SU552373A1/en

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Description

нее отделение 7 снизу ограничено полупроницаемой мембраной 8, котора  герметично прижата к телу  чейки 4 уплотнительным кольцом 9. Дл  слива элюированных фракций в нижнем отделении 7  чейки 4 установлен штуцер 10.its compartment 7 is bounded below by a semipermeable membrane 8, which is hermetically pressed against the body of the cell 4 with a sealing ring 9. A fitting 10 is installed to drain the eluted fractions in the lower compartment 7 of cell 4.

Аппарат работает следующим образом.The device works as follows.

Вырезанные из блока полиакриламидного гел  отдельные -белковые фракции размельчаютс  п помещаютс  в верхнее отделение 6  чейки 4. Верхн   электродна  секци  1 устанавливаетс  в нижней 2, и обе секции заливаютс  электродным буферным раствором так, чтобы уровень буфера в нижней секции 2 был выше полупроницаемой мембраны в. При подаче на электроды 3 аппарата выпр мленного напр жени  белковые компоненты мигрируют из гел  в нижнее отделение 7  чейки 4, скапливаютс  там и вывод тс  по истечении определенного времени через штуцер 10.The individual protein fractions cut from the polyacrylamide gel block are crushed and placed in the upper compartment 6 of cell 4. The upper electrode section 1 is installed in the lower 2, and both sections are filled with electrode buffer solution so that the level of the buffer in the lower section 2 is above the semipermeable membrane in. When a straightened voltage is applied to the electrodes 3 of the apparatus, protein components migrate from the gel to the lower compartment 7 of cell 4, accumulate there and are released after a certain time through fitting 10.

Така  конструкци  аппарата, благодар  наличию верхнего отделени   чейки, отделенного сеткой, позвол ет работать с измельченным гелем, обеспечива  получение отдельных фракций с выходом до 92-95% за минимальное врем . Наличие нижнего отделени  меньшего объема позвол ет сконцентрировать выделение фракции в значительно меньшем объеме, чем они содержались в геле. Простота и разборность конструкции облегчают работу на аппарате и исключают возможность загр знени  выдел емы.х фракций другими компонентами.This design of the apparatus, due to the presence of the upper compartment of the cell, separated by a mesh, allows working with the crushed gel, providing separate fractions with a yield of up to 92-95% in the shortest time. The presence of a lower compartment of smaller volume allows the fraction of the fraction to be concentrated in a much smaller volume than they were contained in the gel. The simplicity and disassembly of the design facilitates the work on the apparatus and eliminates the possibility of contamination of the excreted fractions by other components.

Claims (2)

1.Патент США 3539494, кл. 204-299, 1970.1. US Patent 3539494, cl. 204-299, 1970. 2.Патент США № 3255100, кл. 204-180, 1966 (прототип).2. US patent number 3255100, cl. 204-180, 1966 (prototype). 10ten .ff.ff 7 -97 -9 СЖТULT
SU2080651A 1974-12-03 1974-12-03 Electrophoretic Elution Apparatus SU552373A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU2080651A SU552373A1 (en) 1974-12-03 1974-12-03 Electrophoretic Elution Apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU2080651A SU552373A1 (en) 1974-12-03 1974-12-03 Electrophoretic Elution Apparatus

Publications (1)

Publication Number Publication Date
SU552373A1 true SU552373A1 (en) 1977-03-30

Family

ID=20602428

Family Applications (1)

Application Number Title Priority Date Filing Date
SU2080651A SU552373A1 (en) 1974-12-03 1974-12-03 Electrophoretic Elution Apparatus

Country Status (1)

Country Link
SU (1) SU552373A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4576702A (en) * 1984-11-05 1986-03-18 International Biotechnologies, Inc. Analytical electroelution device
US4576703A (en) * 1984-11-05 1986-03-18 International Biotechnologies, Inc. Preparatory electroelution device
US4725348A (en) * 1984-05-09 1988-02-16 Max-Planck-Gesellschaft Zur Foerderung Der Wissenschaften E.V. Device for the elution of electrically-charged macromolecules

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4725348A (en) * 1984-05-09 1988-02-16 Max-Planck-Gesellschaft Zur Foerderung Der Wissenschaften E.V. Device for the elution of electrically-charged macromolecules
US4576702A (en) * 1984-11-05 1986-03-18 International Biotechnologies, Inc. Analytical electroelution device
US4576703A (en) * 1984-11-05 1986-03-18 International Biotechnologies, Inc. Preparatory electroelution device

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