TFAB002s exhibited binding affinity towards FcRn.

TFAB002s exhibited binding affinity towards FcRn.

<p>FACS was performed to assess TFAB002s’ binding ability with FcRn on H_FCGR2B CHO-K1 cells (A) at pH 6.0 and (B) at pH 7.4.</p>

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Bibliographic Details
Main Author:	Qinghong Li (5003339) (author)
Other Authors:	Kunming Zhang (5919659) (author), Yao Yu (137213) (author), Zeng Yu (2286916) (author), Jingyi Xu (6522) (author), Wenyan Shen (5333102) (author), Lin Zhang (8926) (author), Aidong Qu (11566824) (author), Hongyuan Liang (9909840) (author)
Published:	2024
Subjects:	Biophysics Biochemistry Cell Biology Pharmacology Biotechnology Immunology Cancer Hematology Biological Sciences not elsewhere classified Chemical Sciences not elsewhere classified moderate binding affinity express varying levels encompass various subtypes binding fragment 002 dependent bispecific fab dependent bispecific antibodies selectively depleting cd20 thereby triggering target viable treatment option tumor cell lysis positive b cells div >< p specifically target cd20 optimal target thereby warranting constructing fab therapeutic antibodies novel cd20 vivo </ vitro </ tfab002 ), tandem antigen results underscore novel non normal tissues malignant b heterogeneous group expressing b cytokine release clinical evaluation cell lymphoma cell activation
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