Benmelstobart Biosimilar - Research Grade

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SKU
ICH5388-10mg
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Benmelstobart Biosimilar - Research Grade

Endotoxin
≤ 1.0 EU/mg as determined by the LAL method
Purity
>90% by SDS-PAGE
Species Reactivity
Human
Target
PD-L1
Concentration
>1mg/ml
Isotype
IgG1 - kappa
Host
CHO Cells
Sequence
https://www.imgt.org/mAb-DB/
Buffer
ICH3002
Uniprot
Q9NZQ7
Shipping Conditions
Blue ice
Background
ICH5388 is a research-grade biosimilar of benmelstobart, an anti-PD-L1 monoclonal antibody. It is supplied as an unconjugated, non-therapeutic analog built around the PD-L1 target, intended strictly for research use (RUO) and not for clinical or diagnostic application. Benmelstobart (also known as TQB2450) is a humanized IgG1 antibody that binds programmed death-ligand 1 and blocks its engagement of PD-1, thereby relieving the inhibitory signal that tumors use to evade T-cell attack. This biosimilar reproduces the target specificity of the originator to serve as a reference and control reagent in immuno-oncology workflows. As a human IgG1-kappa format directed against a human antigen, it is well suited to in-vitro and functional characterization rather than routine mouse in-vivo dosing. It is manufactured to a low-endotoxin research grade (<1 EU/mg) and is available in bulk milligram-to-gram quantities, making it appropriate for assay development, binding and neutralization studies, and comparability or benchmarking work where consistent, well-characterized material is required. PD-L1 (programmed death-ligand 1; CD274, UniProt Q9NZQ7) is a type I transmembrane glycoprotein of the B7 immunoglobulin superfamily. It is expressed on antigen-presenting cells, various normal tissues, and is frequently upregulated on tumor cells and within the tumor microenvironment, often driven by interferon-gamma. By binding its receptor PD-1 on activated T cells, PD-L1 delivers an inhibitory signal that dampens T-cell proliferation, cytokine production, and cytotoxic activity, promoting peripheral tolerance. Tumors exploit this axis to escape immune surveillance. PD-L1 also engages CD80 (B7-1). Antibodies that block the PD-L1/PD-1 interaction restore effector T-cell function and underpin a major class of cancer immunotherapies, making PD-L1 a central node in immune-checkpoint research.
Other Names
CD274 
Purification Method
This monoclonal antibody was purified using Protein A
Formulation
Sterile, preservative-free, solution in PBS. BSA and Azide free.
Storage
This biosimilar is stable when stored at 2-8°C. For longer term storage (> 3 months) it is recommended to store this antibody at -20°C or -70°C.
Applications
Functional Assays
Application Notes
This biosimilar is for research use only (RUO): it is not for diagnostic or therapeutic procedures and cannot be purchased by patients.
Use
Products are for research use only. Not for use in diagnostic or therapeutic procedures.
Delivery Time
3-4 weeks
Faq (q&a)

Q: Is the Benmelstobart biosimilar available in gram quantities?

A: Yes — it is manufactured in scalable milligram to gram quantities to support bulk and high-throughput preclinical experiments.


Q: Is this research-grade Benmelstobart biosimilar suitable for in vivo studies?

A: Yes, it is supplied in a low-endotoxin, in vivo-ready formulation intended for preclinical and in vivo research use only (RUO).


Q: What does the Benmelstobart biosimilar target?

A: It is an unconjugated, non-therapeutic research analog of Benmelstobart that binds PD-L1; for research use only.


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Is the Benmelstobart biosimilar available in gram quantities?

Yes — it is manufactured in scalable milligram to gram quantities to support bulk and high-throughput preclinical experiments.

Is this research-grade Benmelstobart biosimilar suitable for in vivo studies?

Yes, it is supplied in a low-endotoxin, in vivo-ready formulation intended for preclinical and in vivo research use only (RUO).

What does the Benmelstobart biosimilar target?

It is an unconjugated, non-therapeutic research analog of Benmelstobart that binds PD-L1; for research use only.

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