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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Description
Summary:<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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