免疫细胞化学
单克隆抗体
分子生物学
生物
中国仓鼠卵巢细胞
抗体
流式细胞术
克隆(Java方法)
免疫疗法
免疫学
细胞培养
免疫系统
生物化学
基因
内分泌学
遗传学
作者
Hiroyuki Suzuki,Masaki Saito,Teizo Asano,Tomohiro Tanaka,Kaishi Kitamura,Yuma Kudo,Mika K. Kaneko,Yukinari Kato
标识
DOI:10.1089/mab.2022.0002
摘要
The C-C motif chemokine receptor 8 (CCR8) is highly expressed in regulatory T cells. CCR8 is also expressed in many cancers and is associated with those progression. The development of monoclonal antibodies (mAbs) for CCR8 leads to cancer immunotherapy and elucidation of unknown mechanisms of CCR8-dependent cancer progression. In this study, we have developed an anti-mouse CCR8 (mCCR8) mAb (clone C8Mab-3, rat IgG1, kappa) using the Cell-Based Immunization and Screening (CBIS) method. We revealed that C8Mab-3 and its recombinant antibody (recC8Mab-3) bind to mCCR8-overexpressed Chinese hamster ovary (CHO)-K1 cells (CHO/mCCR8), but not to the parental CHO-K1 cells, in flow cytometry. In addition, C8Mab-3 and recC8Mab-3 reacted to P388 (a mouse lymphocyte-like cell) and J774-1 (a mouse macrophage-like cell), which express endogenous mCCR8. C8Mab-3 also detected exogenous and endogenous mCCR8 using immunocytochemistry. These results suggest that C8Mab-3, developed using the CBIS method, is useful for immunocytochemistry against exogenous and endogenous mCCR8.
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