>>Signaling Pathways>> Apoptosis>> PD-1/PD-L1 interaction>>Envafolimab

Envafolimab (Synonyms: ASC 22; KN 035)

Catalog No.GC66344

Envafolimab(ASC 22; KN 035)은 인간화 단일 도메인 항 PD-L1 항체의 재조합 단백질입니다. 821d96072c2d58d8970e76f526b0f6b8Envafolimab은 인간 IgG1 항체의 Fc 단편과 항-PD-L1 도메인의 융합에 의해 생성됩니다. 821d96072c2d58d8970e76f526b0f6b8Envafolimab은 5.25nm의 IC50 값으로 PD-L1과 PD-1 사이의 상호 작용을 차단합니다. 821d96072c2d58d8970e76f526b0f6b8Envafolimab은 항종양 활성을 나타냅니다. 821d96072c2d58d8970e76f526b0f6b8Envafolimab은 고형 종양 연구에 잠재력이 있습니다.821d96072c2d58d8970e76f526b0f6b8

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Envafolimab Chemical Structure

Cas No.: 2102192-68-5

Size 가격 재고 수량
5mg
US$1,350.00
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

Envafolimab (ASC 22; KN 035) is a recombinant protein of a humanized single-domain anti- PD-L1 antibody. Envafolimab is created by a fusion of the of anti-PD-L1 domain with Fc fragment of human IgG1 antibody. Envafolimab blocks interaction between PD-L1 and PD-1 with an IC50 value of 5.25 nm. Envafolimab shows antitumor activity. Envafolimab has the potential for the research of solid tumors[1][2][3].

Envafolimab (0-2.51 nM) induces T-cell cytokine (IFN-γ) production in a dose- and time-dependent manner[3].

Envafolimab (0.18-0.92 mg/kg; i.p.; four times over 2 weeks) shows antitumor activity with a half-life of ~72 h in NOD-SCID mice (A375 cells)[3].

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