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Analysis of thrombin-antithrombin complex formation using microchip electrophoresis and mass spectrometry.

Electrophoresis. 2019; 
Nielsen JB, Nielsen AV, Carson RH, Lin HL, Hanson RL, Sonker M, Mortensen DN, Price JC, Woolley AT.
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Recombinant Proteins P1 and CRF came from GenScript (Piscataway, NJ), T and AT were from Haematolgic Technology (Essex Junction, VT), P2 was obtained from Biomatik (Wilmington, DE), TNF came from ProSpec (East Brunswick, NJ), and Hep (estimated 16.5 kDa average) was from Alfa Aesar (Haverhill, MA). Get A Quote

摘要

Preterm birth (PTB) related health problems take over one million lives each year, and currently, no clinical analysis is available to determine if a fetus is at risk for PTB. Here, we describe the preparation of a key PTB risk biomarker, thrombin-antithrombin (TAT), and characterize it using dot blots, MS, and microchip electrophoresis (μCE). The pH for fluorescently labeling TAT was also optimized using spectrofluorometry and spectrophotometry. The LOD of TAT was measured in μCE. Lastly, TAT was combined with six other PTB risk biomarkers and separated in μCE. The ability to make and characterize TAT is an important step toward the development of an integrated microfluidic diagnostic for PTB risk.,? 2019 ... More

關鍵詞

Biomarkers; Disease diagnosis; Dot blot; Point-of-care diagnostics; Protein surface modification
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