@ARTICLE{Li_X._Molecular_2019,
 author={Li, X. and Liu, M. and Bai, X. and Li, Y. and Zhao, Y. and Wang, S. and Wang, J.},
 volume={vol.22},
 number={No 1},
 journal={Polish Journal of Veterinary Sciences},
 pages={143-150},
 howpublished={online},
 year={2019},
 publisher={Polish Academy of Sciences Committee of Veterinary Sciences},
 publisher={University of Warmia and Mazury in Olsztyn},
 abstract={Osteocalcin is a major non-collagenous component of the bone extracellular matrix and is considered to be an indicative factor of osteoblast differentiation. In the present study, we detected osteocalcin expression in different antler areas and growth phases by immunohisto- chemistry. Osteocalcin was highly expressed in all areas during the mineralization period and in mesenchymal cell and chondrocyte areas during the rapid growth period. The nucleotide sequence of the osteocalcin gene in sika deer antler was determined. The open reading frame was 303 bp encoding a protein of 100 amino acids. The estimated molecular mass of osteocalcin was 10.38 kDa and the theoretical isoelectric point was 5.37. The osteocalcin gene with a 6× His-tag at the C-terminus was cloned into the pGEX-4T1 vector and expressed in Escherichia coli under optimal conditions. The recombinant soluble protein fused with GST was purified with Ni-NTA resin. The purified osteocalcin protein exhibited a significant increase in HA adhesion and promoted antler chondrocyte proliferation. Osteocalcin is an important factor in regulating the rapid growth and differentiation of deer antlers.},
 type={Article},
 title={Molecular cloning, recombinant expression, and purification of osteocalcin in sika deer (Cervus nippon) antler},
 URL={http://ochroma.man.poznan.pl/Content/109605/PDF/19.pdf},
 doi={10.24425/pjvs.2018.125613},
 keywords={Cervus nippon, osteocalcin, molecular cloning, expression, purification},
}