Literature DB >> 2302198

Purification and measurement of calpromotin, the cytoplasmic protein which activates calcium-dependent potassium transport.

R B Moore1, G A Plishker, S K Shriver.   

Abstract

A simple procedure is described for the purification of calpromotin, a protein from the cytoplasm of red blood cells which is capable of activating calcium-dependent potassium transport. The purification steps involve a salt gradient elution from an anion exchange column (Whatman DE-52) followed by a potassium phosphate gradient elution from a column of hydroxyapatite (HA Ultrogel). These steps result in a 54% yield with a 161 fold purification. The calpromotin is estimated to be 99% pure as determined by densitometry of the protein profile on an SDS polyacrylamide gel. A competitive enzyme-linked immunosorbent assay (ELISA) using rabbit anti-human calpromotin antibodies, is described for measuring levels of calpromotin in the 5 to 100 ng range.

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Year:  1990        PMID: 2302198     DOI: 10.1016/0006-291x(90)91923-g

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  1 in total

1.  Cytoplasmic calcium buffers in intact human red cells.

Authors:  T Tiffert; V L Lew
Journal:  J Physiol       Date:  1997-04-01       Impact factor: 5.182

  1 in total

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