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Shikari® (S-ATP) Anti-Pembrolizumab ELISA w/confirmation

Enzyme immunoassay for the quantitative determination (screening) of antibodies to Pembrolizumab (Keytruda®) in serum and plasma with confirmation.

This kit has been especially developed for the quantitative determination of antibodies to pembrolizumab in serum and plasma samples.

Pembrolizumab (Keytruda®) was associated to the development of anti-Pembrolizumab antibodies, even some were reported to be neutralizing, in various percentages of patients during therapy with the drug Keytruda®. This might lead to severe complications. This kit can be efficiently used for monitoring anti-Pembrolizumab antibodies during therapy and offers the clinician a tool for decision on possible preventive measures such as possible addition of immunosuppressive drug to reduce anti-Pembrolizumab antibodies. 

All SHIKARI® ELISA kits are suitable for biosimilar work.

All SHIKARI® ELISA kits are produced under ISO 13485 quality system.

Research Use Only (RUO)

For technical inquiry, IFU and other relevant documents please contact techsupport@matriksbiotek.com

 

 

 

Required Volume (µl) 20
Total Time (min) 140
Sample Serum, plasma
Sample Number 96
Detection Limit (ng/mL) 7,5
Spike Recovery (%) Between 85-115
Shelf Life (year) 1
Assay type Quantitative
Species Reactivity Human
Storage conditions Store at +4°C. Please refer to protocols.
Shipping conditions At room temperature
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Safety Data Sheet (SDS) Download

Publications with this drug

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Martinez, C., et al. "374P: Prognostic relevance of post-cycle 1 pembrolizumab levels in real-world NSCLC patients receiving first line IO or ChIO." Journal of Thoracic Oncology 20.3 (2025): S220-S221. Visit Link
Martínez-Toledo, Cristina, et al. "Early Pembrolizumab Plasma Levels as a Prognostic Biomarker in Real-World NSCLC Patients." Pharmacological Research (2026): 108232. Download
Vázquez-Quiroga, Sara, et al. "Evaluation of the exposure-response relationship of pembrolizumab in non-small cell lung cancer: observational study protocol in real-world clinical practice." BMC Cancer 26.1 (2026): 630. Visit Link