单克隆抗体
流式细胞术
生物
趋化因子受体
免疫学
抗体
分子生物学
趋化因子
CCL22型
炎症
作者
Tomohiro Tanaka,Ren Nanamiya,Junko Takei,Takuro Nakamura,Miyuki Yanaka,Hideki Hosono,Masato Sano,Teizo Asano,Mika K. Kaneko,Yukinari Kato
标识
DOI:10.1089/mab.2021.0005
摘要
CC chemokine receptor 8 (CCR8) belongs to the class A of G protein-coupled receptor. It is highly expressed on Treg and T helper 2 (TH2) cells recruited to the inflammation site and is implicated in allergy and asthma. Recently, CCR8+Treg cells have been suggested to be a master regulator in the immunosuppressive tumor microenvironment; therefore, developing sensitive monoclonal antibodies (mAbs) for CCR8 has been desired. This study established a specific and sensitive mAb for mouse CCR8 (mCCR8), which is useful for flow cytometry by using the Cell-Based Immunization and Screening (CBIS) method. The established anti-mCCR8 mAb, C8Mab-2 (rat IgG2b, kappa), reacted with mCCR8-overexpressed Chinese hamster ovary-K1 (CHO/mCCR8) cells and P388 (mouse lymphoid neoplasma) or J774-1 (mouse macrophage-like) cells, which express endogenous mCCR8 by flow cytometry. C8Mab-2, which was established by the CBIS method, could be useful for elucidating the mCCR8-related biological response by flow cytometry.
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