Analysis of the expression of porcine CD200R1 and CD200R1L by using newly developed monoclonal antibodies
Developmental & Comparative Immunology, ISSN: 0145-305X, Vol: 100, Page: 103417
2019
- 5Citations
- 13Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations5
- Citation Indexes5
- CrossRef2
- Captures13
- Readers13
- 13
Article Description
CD200R1 and CD200R1-like are paired receptors which modulate activation of immune cells. Here, we describe the characterisation of their porcine homologues. Analysis of database porcine sequences shows an exceptionally high homology between the extracellular Ig-like domains of these receptors, being the rest more dissimilar. We have obtained two mAbs, PCT1 and PCT3, against a CD200R1-Fc recombinant protein, that bind on CHO cells expressing GFP-tagged CD200R1. The specificity of these mAbs was analysed on CD200R1 L, and also on a CD200R1 splicing variant that lacks the V-type Ig domain. PCT1 bound to both CD200R1 and CD200R1L, but not to the splicing variant, what suggests that recognises an epitope in the V-type Ig domain. PCT3 reacted with both CD200R1 variants, but not CD200R1L, probably binding to an epitope in the N-terminal sequence of CD200R1. Analysis of porcine cells with these mAbs showed expression of CD200R1/CD200R1L on B cells, monocytes and alveolar macrophages.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0145305X19301946; http://dx.doi.org/10.1016/j.dci.2019.103417; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85067881497&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/31233758; https://linkinghub.elsevier.com/retrieve/pii/S0145305X19301946; https://dx.doi.org/10.1016/j.dci.2019.103417
Elsevier BV
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