Antibodies to different peptides in osteopontin reveal complexities in the various secreted forms
β Scribed by Shigeyuki Kon; Masahiro Maeda; Tatsuya Segawa; Yoshiaki Hagiwara; Yuko Horikoshi; Shunsuke Chikuma; Kumiko Tanaka; Mohammod Mizanur Rashid; Manabu Inobe; Ann F. Chambers; Toshimitsu Uede
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 332 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
β¦ Synopsis
We have generated synthetic peptides corresponding to various portions of human osteopontin (OPN) and have immunized rabbits and mice with these peptides to generate polyclonal and monoclonal antibodies specific to human OPN. We then generated six distinct sandwich enzyme-linked immunoabsorbent assay (ELISA) systems by using different pairs of polyclonal and monoclonal antibodies against human OPN. These systems allowed us to detect not only various isoforms and truncated forms of recombinant OPN, but also the glycosylated form of native urinary OPN. Most importantly, tumor-derived OPN was differentially detected by the six ELISA systems. The ELISA systems that we have developed will be useful for clarifying the functional roles for OPN in vivo in various physiologic and pathologic conditions.
π SIMILAR VOLUMES
An immunocytological study of four different parts of the gut of Helix aspersa clearly demonstrates the presence of many cells and fibers immunoreactive toward antibodies directed to vertebrate (Ξ±, Ξ²-endorphin, Ξ±, Ξ²-MSH, ACTH 1-24 and ACTH 17-39, met-enkephalin, somatostatin, insulin, glucagon, P.P.
## Abstract ## Objective The HLA shared epitope (SE) alleles are primarily a risk factor for the presence of antibodies to cyclic citrullinated peptide (antiβCCP antibodies) rather than for the development of rheumatoid arthritis (RA). The SE alleles interact with the environmental risk factor tob