Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P01275 (glucagon)
 26,492 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Antibodies were readily produced in three rabbits to unconjugated pure natural porcine secretin, and in two rabbits to synthetic porcine secretin conjugated to BSA. The final dilutions of the antisera to bind 50% of 1 fmol 125-i-labeled secretin prepared by the Chloramine-T method and purified on a Sephadex G-15 and a SP Sephadex C-25 column varied between 1:14,500 and 1:245,000. The effective equilibrium constants (Keff) according to Scatchard varied between 0.8 x 10(11) and 3.4 x 10(11), the average equilibrium constants (Ko) according to Sips varied between 0.8 x 10(11) and 3.6 x 10(11), and the indices of heterogeneity (alpha) according to Sips were 1.00 or close to 1.00. None of the antisera showed any cross reactivity to gastrin, glucagon or insulin. There was no differences in any of the preceding parameters between the antisera produced to the two immunogen preparations. It is suggested that the immunogenicity of secretin may be related to its basic charge, and to the possibility that secretin may circulate bound to certain plasmafactors or in a polymerized form. The two antisera with the highest equilibrium constants, which also allowed the highest working dilution to be applied, allowed measurements of fasting plasma secretin levels in the low pmol/1 range in all acidified plasmas examined.
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PMID:Production and evaluation of secretin antibodies. 65 47

Antibody was readily produced in a rabbit against synthetic porcine secretin coupled to BSA. The final dilution of the antiserum to bind 50% of 1 fmol 125I-labeled secretin was 1 : 150,000. The effective equilibrium constant (Keff) according to Scatchard was 3.4 X 10(11) l/mol, the average equilibrium constant (Ko) according to Sips 3.5 X 10(11) l/mol, and the index of heterogeneity (alpha) according to Sips 1,00. No cross reactivity was found for gastrin, glucagon and insulin. 125I-labeled synthetic porcine secretin was prepared by the Chloramine-T-method, and the label purified on a Sephadex G-15 column followed by a SP Sephadex C-25 column had a specific radioactivity of 1.150 muCi/nmol. The radioimmunoassay method described has a detection limit of 1.6 pmol/l with 95% confidence limit, a within assay precision of 9,6%, and a between assay precision of 12.8%. It allows detection of fasting plasma secretin in the low pmol/l range, and the rather sharp rise and fall in plasma secretin subsequent to a brief period of duodenal acidification. The problem involved in measuring plasma secretin have been overcome by acidification of the plasma, and by subtracting the "apparent" secretin concentration in corresponding secretin-free plasma prepared by incubation at 37 degrees C for 96 h for each subject.
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PMID:Radioimmunoassay of secretin in acidified plasma. 72 17