Severity: Warning
Message: opendir(/var/lib/php/sessions): Failed to open directory: Permission denied
Filename: drivers/Session_files_driver.php
Line Number: 365
Backtrace:
File: /var/www/html/index.php
Line: 317
Function: require_once
98%
921
2 minutes
20
Isatoic anhydride (IA) has been shown to be a useful platform for quantifiable bioconjugation. The elaboration of a water-soluble isatoic anhydride-based platform with biotin offers readily quantifiable biotinylation reagents through nondestructive methods of quantification. The incorporation of functionality is directly quantified using the reagent's unique absorbance or fluorescence signature, located outside the biological window. Several biotinylation reagents are prepared with various linker lengths, and the quantification of biotinylated proteins is demonstrated and compared to results from the traditional HABA assay.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.bioconjchem.1c00150 | DOI Listing |
Colloids Surf B Biointerfaces
December 2025
Department of Medical Physics, Graduate School of Medicine, Tohoku University, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan; International Center for Synchrotron Radiation Innovation Smart (SRIS), Tohoku University, 2-1-1, Katahira, Aoba-ku, Sendai 980-8577, Japan. Electronic address: kohsu
For precision medicine, it is necessary to quantify the expression levels of marker proteins as well as their micro-regional densities. Many techniques are available for evaluating protein expression levels on tissue sections of patients in order to assess the malignancy of cancer and predict drug efficacy. These technologies, however, have not achieved sufficiently accurate clinical outcome predictions.
View Article and Find Full Text PDFPLoS One
August 2025
Department of Physiology, McGill University, Montreal, Quebec, Canada.
Background: Cells respond to physiological or pathological stimuli by altering the composition of the proteins they produce. This adaptation includes changes to newly translated polypeptides that are destined for intracellular compartments or secretion. The secretome is relevant to cell physiology, as it promotes autocrine, paracrine, and endocrine signaling.
View Article and Find Full Text PDFNanoscale Adv
July 2025
Department of Chemical and Biomolecular Engineering, North Carolina State University Raleigh NC 27695 USA
Plasmonic coupling-based biosensors have been conventionally quantified by bulk spectroscopic or color measurement methods. Such detection schemes limit assay sensitivity due to the high background noise of bulk measurement. In this work, we developed a digital plasmonic assay platform for sensitive biomarker detection by enumerating individual plasmon-shifted nanoclusters single-nanoparticle darkfield scattering imaging.
View Article and Find Full Text PDFPorcine Health Manag
July 2025
College of Veterinary Medicine, Hunan Agricultural University, Changsha, 410125, China.
Background: Porcine Circovirus 2 (PCV2) vaccination plays a crucial role in preventing porcine circovirus-associated disease (PCVAD). Nevertheless, pig farms face significant challenges in evaluating vaccination efficacy due to the inability of PCV2 vaccines to achieve sterilizing immunity and the variability among vaccine manufacturers. These challenges are further compounded by the limitations of conventional antibody detection methods, which fail to distinguish between maternally-derived antibodies (MDAs) and vaccine-induced antibodies.
View Article and Find Full Text PDFSci Rep
July 2025
Centre for Antimicrobial Optimisation, Imperial College London, London, UK.
Antibiotic optimisation through therapeutic drug monitoring (TDM) is a key strategy in tackling antimicrobial resistance. However, current quantification methods rely on laboratory-based equipment, delaying timely dose adjustments. We developed a novel point-of-care lateral flow assay (LFA) for the quantification of vancomycin in serum.
View Article and Find Full Text PDF