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Purification of Human Angiotensinogen
SUMMARY A four-step method for the purification of human angiotensinogen has been devised. The four steps are(1) removal of albumin by affinity chromatography on blue dextran-Sepharose, (2) chromatography on DEAESephadex, (3) chromatography on hydroxylapatite, and (4) chromatography on DEAE-cellulos...
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Published in: | Circulation research 1977-10, Vol.41 (4 Suppl II), p.II-29-33-29-33 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | SUMMARY A four-step method for the purification of human angiotensinogen has been devised. The four steps are(1) removal of albumin by affinity chromatography on blue dextran-Sepharose, (2) chromatography on DEAESephadex, (3) chromatography on hydroxylapatite, and (4) chromatography on DEAE-cellulose. This method is capable of producing 8 mg of purified angiotensinogen from 150 ml of plasma with 33% overall recovery of reninreleasable angiotensin I. The angiotensinogen appears homogeneous by immunochemical and ultracentrifugal techniques. The N-terminal amino acids have been determined to be alanine and aspartic acid or asparagine. |
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ISSN: | 0009-7330 1524-4571 |
DOI: | 10.1161/01.res.41.4.29 |