Mercodia Glucagon ELISA – a Gold Standard
The Mercodia Glucagon ELISA’s high sensitivity, specificity, and low CV% have made it become the Gold Standard for glucagon measurements around globally.
The identification and validation of biomarkers in cancer is essential to improve our understanding of the disease.
The emergence of novel cancer biomarkers continues to grow as scientists strive to find promising novel therapeutic targets and new prognostic and predictive markers to fight the disease.
Biomedica offers a range of unique biomarker ELISAs for your research.
High specificity – known target binding sites through mapping data
The unique specificity of the proprietary antibodies used in the Biomedica ELISA kits ensure that the assays only measure the analyte of interest.
The transmembrane protein Neuropilin-1 (NRP1) regulates tumor biology and has been identified as a checkpoint target (ref. 1). High tissue NRP-1 levels are associated with a poor prognosis in breast cancer patients. In a recent study (ref. 2), German researchers have shown that circulating soluble NRP1 serum levels are an independent marker for poor prognosis in early breast cancer. Soluble Neuropilin-1 was quantified in serum with the highly specific NRP1 ELISA from Biomedica.
The secreted extracellular matrix protein Periostin has evolved as a novel therapeutic target and is a robust marker of glioma malignancy and potential tumor recurrence. It has also been implicated in the pathogenesis of breast cancer as high serum levels of periostin are associated with a poor survival in breast cancer patients (ref. 3). Periostin was quantified in serum with the well characterized Biomedica Periostin ELISA that has been published (ref. 4).
Semaphorin 4D (Sema4D) is a glycoprotein that is emerging as clinical biomarker and as therapeutic target in cancer. It has been associated with cancer progression and the occurrence of bone metastases (ref. 5, 6).
Leucine-rich alpha-2-glycoprotein 1 (LRG1) is a protein that is an important factor involved in pathogenic angiogenesis in cancer. It is abundantly present in the microenvironment of many tumors contributing to vascular dysfunction and thus serving as a potential therapeutic target (ref. 7).
The RANKL/RANK/OPG system contributes to the development of bone metastases and influences tumor biology in earlier stages of cancer (ref. 9). Dysregulation has been widely documented in the context of metastatic bone disease (ref. 10). The Biomedica OPG and RANKL ELISA kits have been widely used in the respective studies.
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