RO103684B1 - Production method of immuno-globulin a1(iga1) - Google Patents

Production method of immuno-globulin a1(iga1)

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Publication number
RO103684B1
RO103684B1 RO138173A RO13817389A RO103684B1 RO 103684 B1 RO103684 B1 RO 103684B1 RO 138173 A RO138173 A RO 138173A RO 13817389 A RO13817389 A RO 13817389A RO 103684 B1 RO103684 B1 RO 103684B1
Authority
RO
Romania
Prior art keywords
iga1
nan3
buffer
k2hpo4
nacl
Prior art date
Application number
RO138173A
Other languages
Romanian (ro)
Other versions
RO103684A2 (en
Inventor
Aurel Ionita
Constantina Ionita
Emil Ionita
Original Assignee
Institutul "Cantacuzino"
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 Institutul "Cantacuzino" filed Critical Institutul "Cantacuzino"
Priority to RO138173A priority Critical patent/RO103684B1/en
Publication of RO103684A2 publication Critical patent/RO103684A2/en
Publication of RO103684B1 publication Critical patent/RO103684B1/en

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  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Peptides Or Proteins (AREA)

Abstract

Procedeul conform inventiei consta în aceea ca plasma de mielom IgA1, selectionata a fi cât mai bogata în IgA1 si cât mai saraca în IgG, este defibrinata cu CaCl2 si apoi tratata cu 25 g (NH4)2SO4 la 100 ml la 4 degree C, dupa centrifugare precipitatul se spala de doua ori cu solutie (NH4)2SO4, 25 g 100 ml apa si reluat în tampon Na3PO4/H3PO4 0,03 M pH'5, ce contine 0,3 M NaCl si o,o2% NaN3, apoi cromatografiat pe DEAE Affi Gel-Blue, eluaeea se face cu acelasi tampon si primul peak se concentreaza si se echilibreaza cu tampon K2HPO4 0,02 M pH'8, ce contine 0,02% NaN3 si se trece pe aceeasi coloana cromatografica regenerata si echilibrata cu acest tampon, în final IgA1 este eluata cu 0,1 M NaCl în tampon K2HPO4 0,02 M pH'8, ce contine 0,02 NaN3.The process according to the invention consists in that IgA1 myeloma plasma selected as being as rich in IgA1 and as poor as IgG is defibrinated with CaCl2 and then treated with 25 g (NH4) 2 SO4 per 100 ml at 4 ° C after centrifugation, the precipitate was washed twice with (NH4) 2 SO4 solution, 25 g of 100 mL of water, and resuspended in 0.03 M NaHPO4 / H3PO4 pH5 containing 0.3M NaCl and 0.2% NaN3, then chromatographed on DEAE Affi Gel-Blue, the eluate is made with the same buffer and the first peak is concentrated and equilibrated with K2HPO4 0.02 M pH8 buffer containing 0.02% NaN3 and passed to the same regenerated and balanced chromatographic column this buffer, finally IgA1 is eluted with 0.1 M NaCl in K2HPO4 0.02 M pH8, containing 0.02 NaN3.

RO138173A 1989-02-10 1989-02-10 Production method of immuno-globulin a1(iga1) RO103684B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
RO138173A RO103684B1 (en) 1989-02-10 1989-02-10 Production method of immuno-globulin a1(iga1)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RO138173A RO103684B1 (en) 1989-02-10 1989-02-10 Production method of immuno-globulin a1(iga1)

Publications (2)

Publication Number Publication Date
RO103684A2 RO103684A2 (en) 1991-12-09
RO103684B1 true RO103684B1 (en) 1992-03-25

Family

ID=20123980

Family Applications (1)

Application Number Title Priority Date Filing Date
RO138173A RO103684B1 (en) 1989-02-10 1989-02-10 Production method of immuno-globulin a1(iga1)

Country Status (1)

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RO (1) RO103684B1 (en)

Also Published As

Publication number Publication date
RO103684A2 (en) 1991-12-09

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