Scaled down method for the reproducible recovery to high purity of human serum albumin from low volume blood samples View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2001-05

AUTHORS

M. Rynö, T. Anttinen-Klemetti, R. Vaaranrinta, J. Tornaeus, A. Hesso, T. Veidebaum, K. Peltonen

ABSTRACT

A basic need for a protein-based dosimeter is a purified protein. In this communication we present an isolation protocol and an HPLC-based assay which allows one to determine the purity of the isolated albumin. A total of 168 human blood samples were collected from workers of a benzene processing plant and from nearby countryside at Kohtla-Järve, Estonia. Albumin was isolated from plasma by sequential precipitation and the purity was determined by HPLC. The amount of albumin present in plasma varied between the individuals, being 147 +/- 26 mg/5 ml (n = 168), which is about 59% of plasma albumin. However, the isolated albumin was highly pure (100.9 +/- 8.2%, n = 5). All albumin samples analyzed demonstrate two peaks in HPLC analysis. The two peaks detected were collected and subjected to MS analysis, which demonstrates a difference of 120 mass units between the two albumin products isolated. We have developed an assay, which is easy to carry out and is not too labor intense. The HPLC analysis can be applied to confirm the purity of the isolated albumin as well as to confirm the quantity of the albumin in samples. More... »

PAGES

197-201

Identifiers

URI

http://scigraph.springernature.com/pub.10.1023/a:1016347102660

DOI

http://dx.doi.org/10.1023/a:1016347102660

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1002243433

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/12233742


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164 schema:name Finnish Institute of Occupational Health, Topeliuksenkatu 41 Aa, FIN-00250, Helsinki, Finland
165 Finnish Institute of Occupational Health, Topeliuksenkatu 41 Aa, FIN-00250, Helsinki, Finland Corresponding author
166 rdf:type schema:Organization
 




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