Abstract:
:The bovine oxytocin precursor was expressed in Escherichia coli as a fusion protein by cloning the hormone encoding cDNA in frame behind the replicase gene of the RNA phage MS2. By step-wise extraction with different urea concentrations, the fusion protein was enriched in the 7 M urea fraction and further purified by Sephacryl S-300 chromatography. The oxytocin precursor was cleaved off the fusion protein by cyanogen bromide treatment, chromatographed on FPLC columns and identified by Western blot analysis, using antibodies raised against neurophysin.
journal_name
Biochimiejournal_title
Biochimieauthors
Nörenberg U,Brunath A,Richter Ddoi
10.1016/0300-9084(88)90165-4subject
Has Abstractpub_date
1988-01-01 00:00:00pages
109-17issue
1eissn
0300-9084issn
1638-6183pii
0300-9084(88)90165-4journal_volume
70pub_type
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