Acasunlimab Biosimilar Bispecific Antibody (PD-L1 × 4-1BB) for Research

Cat No.: GMP-Bios-ab-007

Pre-made Acasunlimab benchmark antibody (Bispecific mAb, anti-CD274/PD-L1;TNFRSF9/CD137 therapeutic antibody, Anti-B7-H/B7H1/PDCD1L1/PDCD1LG1/PDL1/hPD-L1;ILA/4-1BB/CDw137 Antibody) is a biosimilar expressed by mammalian cell line as a benchmark reference therapeutic antibody for biological drug disovery items including cell culture, assay development, animal model development, PK/PD model development (Pharmacokinetics & Pharmacodynamic) and mechanism of action (MOA) research.



Order Information

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Catalog No. Package Price(In USD)
GMP-Bios-ab-007-1mg 1mg
GMP-Bios-ab-007-10mg 10mg
GMP-Bios-ab-007-100mg 100mg
GMP-Bios-ab-007-xmg ≥100mg



Product Details

Products Name (INN Index) Pre-Made Acasunlimab biosimilar, Bispecific mAb, Anti-CD274/PD-L1;TNFRSF9/CD137 Antibod: Anti-B7-H/B7H1/PDCD1L1/PDCD1LG1/PDL1/hPD-L1;ILA/4-1BB/CDw137 therapeutic antibody
INN Name Acasunlimab
TargetPD-L1;CD137
FormatBispecific mAb
DerivationBispecific antibody
Species ReactivityHuman
CH1 IsotypeIgG1
VD LCLambda;Kappa
Highest_Clin_Trial (Jan '20)Phase-I/II
Est. StatusActive
100% SI StructureNone;None
99% SI StructureNone;None
95-98% SI StructureNone;None
Year Proposed2020
Year Recommendedna
CompaniesGenmab;BioNTech
Conditions Approvedna
Conditions ActiveSolid tumours
Conditions Discontinuedna
Development Techna



About target - CD274

1. Protein Programmed cell death 1 ligand 1

2. Gene CD274

3. Organism Homo sapiens (Human)

Function

Plays a critical role in induction and maintenance of immune tolerance to self (PubMed:11015443, PubMed:28813417, PubMed:28813410).

As a ligand for the inhibitory receptor PDCD1/PD-1, modulates the activation threshold of T-cells and limits T-cell effector response (PubMed:11015443, PubMed:28813417, PubMed:28813410).

Through a yet unknown activating receptor, may costimulate T-cell subsets that predominantly produce interleukin-10 (IL10) (PubMed:10581077).

The PDCD1-mediated inhibitory pathway is exploited by tumors to attenuate anti-tumor immunity and escape destruction by the immune system, thereby facilitating tumor survival (PubMed:28813417, PubMed:28813410).

The interaction with PDCD1/PD-1 inhibits cytotoxic T lymphocytes (CTLs) effector function (By similarity).

The blockage of the PDCD1-mediated pathway results in the reversal of the exhausted T-cell phenotype and the normalization of the anti-tumor response, providing a rationale for cancer immunotherapy (By similarity).