Lesabelimab Biosimilar - Research Grade

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SKU
ICH5635-10mg
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Lesabelimab 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
ICH5635 is a research-grade, unconjugated recombinant analog of the anti-PD-L1 antibody lesabelimab, built as a human IgG1-kappa reproduction of the originator's binding specificity against human PD-L1 (CD274). It is a non-therapeutic biosimilar intended strictly for research use only, not for human or veterinary use, and it is not the clinical drug. The molecule is useful for laboratory work where a well-characterized, consistent anti-PD-L1 reagent is needed: as a positive or reference control in checkpoint-blockade assays, for benchmarking novel anti-PD-L1 candidates, for studying PD-L1/PD-1 and PD-L1/B7-1 interactions, for ligand-blocking and neutralization experiments, and for supporting ADCC or antibody-drug-conjugate development workflows. Because it is supplied unconjugated, it can be labeled or formatted by the end user. It is manufactured to low-endotoxin specifications (research grade below 1 EU/mg; ultra-low grade below 0.5 EU/mg) and offered in bulk milligram-to-gram quantities suitable for in-vitro assays, cell-based systems, and preclinical model standards, giving researchers lot consistency at a scale useful for larger studies. PD-L1 (programmed death-ligand 1), encoded by CD274 and also called B7-H1, is a type I transmembrane glycoprotein of the B7 immunoglobulin superfamily. It is expressed on many cell types including antigen-presenting cells, epithelial and endothelial cells, and is frequently upregulated on tumor cells, often driven by interferon-gamma in the tumor microenvironment. PD-L1 engages the inhibitory receptor PD-1 (PDCD1) on activated T cells, delivering a co-inhibitory signal that dampens T-cell receptor signaling, cytokine production, and proliferation. It also binds B7-1 (CD80). Through these interactions PD-L1 contributes to peripheral tolerance and immune homeostasis, but tumors exploit the PD-L1/PD-1 axis to evade cytotoxic T-cell responses. Antibodies that block PD-L1 can relieve this suppression and restore antitumor immunity, which is why the axis is a central target in cancer immunotherapy 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 Lesabelimab biosimilar available in bulk mg to gram quantities?

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


Q: Is this research-grade Lesabelimab biosimilar suitable for in vivo use?

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


Q: What does the Lesabelimab biosimilar target?

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


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Is the Lesabelimab biosimilar available in bulk mg to gram quantities?

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

Is this research-grade Lesabelimab biosimilar suitable for in vivo use?

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

What does the Lesabelimab biosimilar target?

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

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