Bony fish use the glycoprotein hormone stanniocalcin (STC) to counteract hy
percalcaemia. This is achieved through dual mechanisms involving gill calci
um uptake inhibition and stimulation of renal inorganic phosphate reabsorpt
ion. Human STC (hSTC-1) shows considerable homology with both rat and mouse
STC (mSTC) and their mRNA is expressed in a wide range of tissues. In fish
, STC is produced by endocrine glands known as the corpuscles of Stannius b
ut in mammals the widespread expression is suggestive of a paracrine rather
than an endocrine role. In order to determine the distribution and structu
ral characteristics of hSTC-1, the recombinant protein was expressed in bac
teria, purified by metal-ion affinity chromatography, and a study was made
of the likely epitopes for raising an antibody. This novel hSTC-1 antibody
was used to test the purification protocol. Since the role of mammalian STC
is largely unknown, the specific distribution of STC needed to be addresse
d. To test the specificity of the antibody, sodium dodecyl sulfate-polyacry
lamide gel electrophoresis (SDS-PAGE)/Western blotting was undertaken in ho
mogenised rat bladder, ovary and kidney.