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Journal articles on the topic 'Biolabel'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Qin, Xiaoli, Aigui Xu, Ling Liu, Wenfang Deng, Chao Chen, Yueming Tan, Yingchun Fu, Qingji Xie, and Shouzhuo Yao. "Ultrasensitive electrochemical immunoassay of proteins based on in situ duple amplification of gold nanoparticle biolabel signals." Chemical Communications 51, no. 40 (2015): 8540–43. http://dx.doi.org/10.1039/c5cc01439e.

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An electrochemical sandwich immunoassay method that can be sensitive to a few protein molecules (human immunoglobulin G or human prostate-specific antigen) is reported based on in situ duple amplification of gold nanoparticle biolabel signals.

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2

Oviedo, M. J., O. E. Contreras, Y. Rosenstein, R. Vazquez-Duhalt, Z. S. Macedo, G. G. Carbajal-Arizaga, and G. A. Hirata. "New Bismuth Germanate Oxide Nanoparticle Material for Biolabel Applications in Medicine." Journal of Nanomaterials 2016 (2016): 1–10. http://dx.doi.org/10.1155/2016/9782625.

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Bismuth germanate (Bi4Ge3O12, BGO) has been the focus of several studies due to its scintillation properties. It has been employed as detector in scientific research and medicine, and herein we studied its possible biomedical applications. The photoluminescence properties of the uncoated and protein-coated nanoparticles were analyzed in different body fluids, at different pH. The nanoparticles yielded blueish-white luminescence with a maximum emission peak at 485 nm corresponding to the3P1→1S0electron transition of Bi3+. They showed luminescence properties at different pH values and in human fluids, such as urine and blood serum. Finally, the BGO nanoparticles were functionalized with the anti-HLA I W6/32 monoclonal antibody and the capacity of the antibody-loaded nanoparticles to recognize the cognate antigen (HLA I) of the W6/32 mAb was assessed on the human promyelocytic leukemia cell line THP-1. The possibility of functionalizing BGO nanoparticles with W6/32 antibodies and their specificity to identify THP-1 cells make them promising candidates for biomedical applications as biolabels.

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3

Bi, Sai, Hong Zhou, and Shusheng Zhang. "Multilayers enzyme-coated carbon nanotubes as biolabel for ultrasensitive chemiluminescence immunoassay of cancer biomarker." Biosensors and Bioelectronics 24, no. 10 (June 2009): 2961–66. http://dx.doi.org/10.1016/j.bios.2009.03.002.

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4

Sun, Ai-Li, Feng-Chun Jia, Yan-Fang Zhang, and Xuan-Nian Wang. "Gold nanocluster-encapsulated glucoamylase as a biolabel for sensitive detection of thrombin with glucometer readout." Microchimica Acta 182, no. 5-6 (December 12, 2014): 1169–75. http://dx.doi.org/10.1007/s00604-014-1440-1.

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5

Zhang, Hui, Lu Tian, Ruoyu Zhang, Zhiqiang Ye, and Jingli Yuan. "Preparation of visible-light-excited luminescence enhancement solutions for time-resolved luminescence detection of europium biolabel." Analyst 137, no. 19 (2012): 4502. http://dx.doi.org/10.1039/c2an35719d.

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6

Gouvêa, A., A. T. Pereira, A. C. Pimentel, D. M. F. Prazeres, V. Chu, and J. P. Conde. "Colorimetric detection of molecular recognition reactions with an enzyme biolabel using a thin-film amorphous silicon photodiode on a glass substrate." Sensors and Actuators B: Chemical 135, no. 1 (December 2008): 102–7. http://dx.doi.org/10.1016/j.snb.2008.07.030.

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7

Li, Xu-Zhao, Hua-Jin Huang, Shuai-Nan Zhang, Qi Liu, and Yu-Mei Wang. "Label-free quantitative proteomics positions the effects and mechanisms of Herba Lysimachiae on synovial diseases based on biolabel-led research pattern." Journal of Chromatography B 1138 (February 2020): 121969. http://dx.doi.org/10.1016/j.jchromb.2020.121969.

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8

Qin, Xiaoli, Aigui Xu, Ling Liu, Yuyun Sui, Yunlong Li, Yueming Tan, Chao Chen, and Qingji Xie. "Selective staining of CdS on ZnO biolabel for ultrasensitive sandwich-type amperometric immunoassay of human heart-type fatty-acid-binding protein and immunoglobulin G." Biosensors and Bioelectronics 91 (May 2017): 321–27. http://dx.doi.org/10.1016/j.bios.2016.12.051.

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9

LI, Xu-zhao, Hong-mei LI, Shuai-nan ZHANG, Qi LIU, and Yu-mei WANG. "A biolabel research based on metabonomics reveals the therapeutic potentials of Herba Lysimachiae in synovial diseases: The dual effects on synovial platelet aggregation by prostaglandin E1/E2." Journal of Chromatography B 1174 (June 2021): 122726. http://dx.doi.org/10.1016/j.jchromb.2021.122726.

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10

Eriksson, E., J. Lysell, H. Larsson, K. Y. Cheung, D. Filippini, and W. C. Mak. "Geometric Flow Control Lateral Flow Immunoassay Devices (GFC-LFIDs): A New Dimension to Enhance Analytical Performance." Research 2019 (June 17, 2019): 1–8. http://dx.doi.org/10.34133/2019/8079561.

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The nitrocellulose (NC) membrane based lateral flow immunoassay device (LFID) is one of the most important and widely used biosensor platforms for point-of-care (PoC) diagnostics. However, the analytical performance of LFID has limitations and its optimization is restricted to the bioassay chemistry, the membrane porosity, and the choice of biolabel system. These bottom neck technical issues resulted from the fact that the conventional LFID design principle has not evolved for many years, which limited the LFID for advanced biosensor applications. Here we introduce a new dimension for LFID design and optimization based on geometric flow control (GFC) of NC membranes, leading to highly sensitive GFC-LFID. This novel approach enables comprehensive flow control via different membrane geometric features such as the width (w) and the length (l) of a constriction, as well as its input angle (θ1) and output angle (θ2). The GFC-LFID (w=0.5 mm, l=7 mm, θ1= 60°, θ2= 45°) attained a 10-fold increase in sensitivity for detection of interleukin-6 (IL-6), compared with conventional LFID, whereas reducing by 10-fold the antibody consumption. The GFC-LFID detects IL-6 over a linear range of 0.1–10 ng/mL with a limit of detection (LoD) of 29 pg/mL, which even outperforms some commercial IL-6 LFIDs. Such significant improvement is attained by pure geometric control of the NC membrane, without additives, that only relaying on a simple high throughput laser ablation procedure suitable for integration on regular large-scale manufacturing of GFC-LFIDs. Our new development on GFC-LFID with the combination of facile scalable fabrication process, tailored flow control, improved analytical performance, and reduced antibodies consumption is likely to have a significant impact on new design concept for the LFID industry.

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11

Zhang, Shuai-nan, Ya-feng He, Xu-zhao Li, Wu-de Yang, and Ying Zhou. "Biolabel-led research pattern positions the effects and mechanisms of Sophorae Tonkinensis radix et rhizome on lung diseases: A novel strategy for computer-aided herbal medicine research based on omics and bioinformatics." Computers in Biology and Medicine 136 (September 2021): 104769. http://dx.doi.org/10.1016/j.compbiomed.2021.104769.

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12

Wood, Jonathan. "Au nanoclusters are promising biolabels." Materials Today 7, no. 10 (October 2004): 18. http://dx.doi.org/10.1016/s1369-7021(04)00440-7.

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13

Pui-yee Chan, Cangel, Matthias Haeussler, Ben Zhong Tang, Yongqiang Dong, King-keung Sin, Wing-cheung Mak, Dieter Trau, Matthias Seydack, and Reinhard Renneberg. "Silole nanocrystals as novel biolabels." Journal of Immunological Methods 295, no. 1-2 (December 2004): 111–18. http://dx.doi.org/10.1016/j.jim.2004.09.016.

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14

Yu, Junhua, Sungmoon Choi, and Robert M Dickson. "Shuttle-Based Fluorogenic Silver-Cluster Biolabels." Angewandte Chemie 121, no. 2 (January 2, 2009): 324–26. http://dx.doi.org/10.1002/ange.200804137.

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15

Yu, Junhua, Sungmoon Choi, and Robert M Dickson. "Shuttle-Based Fluorogenic Silver-Cluster Biolabels." Angewandte Chemie International Edition 48, no. 2 (January 2, 2009): 318–20. http://dx.doi.org/10.1002/anie.200804137.

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16

Ju, Qiang, Datao Tu, Yongsheng Liu, Haomiao Zhu, and Xueyuan Chen. "Lanthanide-Doped Inorganic Nanocrystals as Luminescent Biolabels." Combinatorial Chemistry & High Throughput Screening 15, no. 7 (July 1, 2012): 580–94. http://dx.doi.org/10.2174/138620712801619177.

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17

Chan, Cangel Pui-yee, Yvonne Bruemmel, Matthias Seydack, King-keung Sin, Ling-wai Wong, Elaine Merisko-Liversidge, Dieter Trau, and Reinhard Renneberg. "Nanocrystal Biolabels with Releasable Fluorophores for Immunoassays." Analytical Chemistry 76, no. 13 (July 2004): 3638–45. http://dx.doi.org/10.1021/ac0353740.

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18

Um, Joseph, Yali Zhang, Wen Zhou, Mohammad R. Zamani Kouhpanji, Cosmin Radu, Rhonda R. Franklin, and Bethanie J. H. Stadler. "Magnetic Nanowire Biolabels Using Ferromagnetic Resonance Identification." ACS Applied Nano Materials 4, no. 4 (March 26, 2021): 3557–64. http://dx.doi.org/10.1021/acsanm.1c00086.

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19

Sy, Mohamadou, Aline Nonat, Niko Hildebrandt, and Loïc J. Charbonnière. "Lanthanide-based luminescence biolabelling." Chemical Communications 52, no. 29 (2016): 5080–95. http://dx.doi.org/10.1039/c6cc00922k.

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20

Mozaffari, Mohammad Hazhir, Majid Ebnali-Heidari, Gholamreza Abaeiani, and Mohammad Kazem Moravvej-Farshi. "Photonic crystal optofluidic biolaser." Photonics and Nanostructures - Fundamentals and Applications 26 (September 2017): 56–61. http://dx.doi.org/10.1016/j.photonics.2017.07.002.

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21

Hornemann, Andrea, Diane Eichert, Sabine Flemig, Gerhard Ulm, and Burkhard Beckhoff. "Qualifying label components for effective biosensing using advanced high-throughput SEIRA methodology." Physical Chemistry Chemical Physics 17, no. 14 (2015): 9471–79. http://dx.doi.org/10.1039/c4cp05944a.

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22

Mak, Wing Cheung, Kwan Yee Cheung, Dieter Trau, Axel Warsinke, Frieder Scheller, and Reinhard Renneberg. "Electrochemical Bioassay Utilizing Encapsulated Electrochemical Active Microcrystal Biolabels." Analytical Chemistry 77, no. 9 (May 2005): 2835–41. http://dx.doi.org/10.1021/ac048505l.

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23

Pande, Amrita. "Visa Stamps for Injections: Traveling Biolabor and South African Egg Provision." Gender & Society 34, no. 4 (June 25, 2020): 573–96. http://dx.doi.org/10.1177/0891243220932147.

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In this article, I discuss cross-border egg provision by young South African women as a form of traveling biolabor that is critically about embodiment, and aspirations for mobility and cosmopolitanism. The frame of biolabor challenges the frames of altruism/commodification, and choice/coercion, and instead highlights the desires of egg providers, fundamental to the creation and maintenance of the global fertility market. When biolabor crosses borders as traveling biolabor, the analysis can focus on the specificities of inequalities embedded within such reproductive mobility. Traveling or mobility is often a privileged decision and connotes freedom and cultural capital. Yet, when applied to young white egg providers from South Africa, this traveling biolabor relies on a particular kind of biopolitics wherein the reproductive potential of ova/egg is fundamental in facilitating women’s cross-border mobility. I divide the findings sections into three key themes—“cosmopolitan competency,” “alternatives to maternity,” and “productive pain”—to argue that, on the one hand, from recruitment of traveling egg providers to their (self) management, this biolabor is built on the young women’s aspirations for cosmopolitanism. Traveling biolabor becomes a way to escape the normative expectations of their (primarily rural, conservative) families and the (Afrikaner) national project of the volksmoeder (mother of the nation). On the other hand, the pursuit of these aspirations is critically contingent on management successfully reframing the embodied pain of egg provision as well as the biolaborer’s own maternity. Laborers’ desires and management disciplining tactics converge to sustain the global fertility market.

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24

Jochum, Anne, Nathalie Schlienger, David Egron, Suzanne Peyrottes, and Christian Périgaud. "Biolabile constructs for pronucleotide design." Journal of Organometallic Chemistry 690, no. 10 (May 2005): 2614–25. http://dx.doi.org/10.1016/j.jorganchem.2004.11.015.

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25

Cai, Wenyi, Ian R. Gentle, Gao Qing Lu, Jun-Jie Zhu, and Aimin Yu. "Mesoporous Silica Templated Biolabels with Releasable Fluorophores for Immunoassays." Analytical Chemistry 80, no. 14 (July 2008): 5401–6. http://dx.doi.org/10.1021/ac800430m.

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26

Barnard, Amanda S. "Diamond standard in diagnostics: nanodiamond biolabels make their mark." Analyst 134, no. 9 (2009): 1751. http://dx.doi.org/10.1039/b908532g.

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27

Ostróżka-Cieślik, Aneta, Barbara Dolińska, and Florian Ryszka. "Biochemical Studies in Perfundates and Homogenates of Isolated Porcine Kidneys after Flushing with Zinc or Zinc–Prolactin Modified Preservation Solution Using a Static Cold Storage Technique." Molecules 26, no. 11 (June 7, 2021): 3465. http://dx.doi.org/10.3390/molecules26113465.

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Zinc is an effective anti-inflammatory and antioxidant trace element. The aim of this study was to analyse the protective effect of zinc and zinc–prolactin systems as additives of preservation solutions in the prevention of nephron damage caused during ischemia. The study used a model for storing isolated porcine kidneys in Biolasol®. The solution was modified with the addition of Zn at a dose of 1 µg/L and Zn: 1 µg/L with prolactin (PRL): 0.1 µg/L. After 2 h and 48 h of storage, the levels of alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase, sodium, potassium, creatinine and total protein were determined. Zinc added to the Biolasol® composition at a dose of 1 µg/L showed minor effectiveness in the protection of nephrons. In turn, Zn2+ added to Biolasol + PRL (PRL: 0.1 µg/L) acted as a prolactin inhibitor. We do not recommend the addition of Zn(II) (1 µg/L) and Zn(II) (1 µg/L) + PRL (0.1 µg/L) to the Biolasol solution.

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28

Mesnager, Julien, Vahid Noeei, Omkar Chandorkar, Steven Bloembergen, Doug Ireland, and Masato Katayama. "Advances in Biolatex® Binding Systems." JAPAN TAPPI JOURNAL 68, no. 11 (2014): 1272–79. http://dx.doi.org/10.2524/jtappij.68.1272.

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29

Frenzel, Daniel, and Dieter Willbold. "Kinetic Titration Series with Biolayer Interferometry." PLoS ONE 9, no. 9 (September 17, 2014): e106882. http://dx.doi.org/10.1371/journal.pone.0106882.

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30

Maragos, Chris M. "Detection of deoxynivalenol using biolayer interferometry." Mycotoxin Research 27, no. 3 (February 15, 2011): 157–65. http://dx.doi.org/10.1007/s12550-011-0090-y.

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31

Ostróżka-Cieślik, Aneta, Barbara Dolińska, and Florian Ryszka. "Therapeutic Potential of Selenium as a Component of Preservation Solutions for Kidney Transplantation." Molecules 25, no. 16 (August 7, 2020): 3592. http://dx.doi.org/10.3390/molecules25163592.

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Selenium has strong antioxidant properties and diverse effects on the immune system. The aim of the study was to analyse the protective effect of selenium as a component of a kidney preservation solution on the prevention of ischemia-reperfusion injury of nephrons. The solution was modified by the addition of Se (1 µg/L), prolactin (0.1 µg/L) and Se with prolactin (1 µg/L Se + 0.1 µg/L PRL). The study used a model for storing isolated porcine kidneys in Biolasol® (modified Biolasol®), which minimizes ischemia-reperfusion injury of grafts. The introduction of Se4+ ions at a dose of 1 µg/L into the Biolasol® preservation solution in the form of Na2SeO3 caused an increase in the activity/concentration of the analysed biochemical parameters: aspartate transaminase, alanine transaminase, urea and protein. This suggests an adverse effect of Se4+ on nephron function during ischemia-reperfusion. The best graft protection was obtained by using Biolasol® modified with the addition of selenium (IV) at a dose of 1 µg/L and prolactin at a concentration of 0.1 µg/L. We proposed the mechanism of prolactin action in the metabolic reduction of selenite (SO32−) during ischemia/reperfusion.

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32

Ostróżka-Cieślik, Aneta, Barbara Dolińska, and Florian Ryszka. "Effectiveness Assessment of a Modified Preservation Solution Containing Thyrotropin or Follitropin Based on Biochemical Analysis in Perfundates and Homogenates of Isolated Porcine Kidneys after Static Cold Storage." International Journal of Molecular Sciences 22, no. 16 (August 4, 2021): 8360. http://dx.doi.org/10.3390/ijms22168360.

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In this paper, we assess the nephroprotective effects of thyrotropin and follitropin during ischaemia. The studies were performed in vitro in a model of isolated porcine kidneys stored in Biolasol (FZNP, Biochefa, Sosnowiec, Poland) and modified Biolasol (TSH: 1 µg/L; FSH 1 µg/L). We used the static cold storage method. The study was carried out based on 30 kidneys. The kidneys were placed in 500 mL of preservation solution chilled to 4 °C. The samples for biochemical tests were collected during the first kidney perfusion (after 2 h of storage) and during the second perfusion (after 48 h of storage). The results of ALT, AST, and LDH activities confirm the effectiveness of Biolasol + p-TSH in maintaining the structural integrity of renal cell membranes. Significantly reduced biochemical parameters of kidney function, i.e., creatinine and protein concentrations were also observed after 48 h storage. The protective effect of Biasol + p-TSH is most pronounced after 2 h of storage, suggesting a mild course of damage thereafter. A mild deterioration of renal function was observed after 48 h. The results of our analyses did not show any protective effect of Biolasol + p-FSH on the kidneys during ischaemia.

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33

Lawler, A. "Gavel Falls on Biolab." Science 313, no. 5788 (August 11, 2006): 747d. http://dx.doi.org/10.1126/science.313.5788.747d.

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34

Kintisch, E. "Biolab Set to Open." Science 314, no. 5797 (October 13, 2006): 235c. http://dx.doi.org/10.1126/science.314.5797.235c.

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35

Li, Honglan, Guixia Liu, Jinxian Wang, Xiangting Dong, and Wensheng Yu. "Dual-mode, tunable color, enhanced upconversion luminescence and magnetism of multifunctional BaGdF5:Ln3+ (Ln = Yb/Er/Eu) nanophosphors." Physical Chemistry Chemical Physics 18, no. 31 (2016): 21518–26. http://dx.doi.org/10.1039/c6cp03743g.

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BaGdF₅:Yb³⁺,Er³⁺/Eu³⁺ nanophosphors were prepared by a hydrothermal method, and the energy transfer, color-tunable dual-mode emissions and magnetic properties were studied, which could have promising applications in the fields of LEDs, MRI, biolabels, and so on.

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36

Xu, Gaixia, Ken-Tye Yong, Indrajit Roy, and Atcha Kopwitthaya. "FGF2-Labeled Semiconductor Nanocrystals as Luminescent Biolabels for Imaging Neuroblastoma Cells." Journal of Biomedical Nanotechnology 6, no. 6 (December 1, 2010): 641–47. http://dx.doi.org/10.1166/jbn.2010.1164.

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37

Mayer, Ludovic, Abdallah Slablab, Géraldine Dantelle, Vincent Jacques, Aude-Marie Lepagnol-Bestel, Sandrine Perruchas, Piernicola Spinicelli, et al. "Single KTP nanocrystals as second-harmonic generation biolabels in cortical neurons." Nanoscale 5, no. 18 (2013): 8466. http://dx.doi.org/10.1039/c3nr01251d.

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38

Philippidis, Alex. "New England Biolabs Looks Past Enzymes." Genetic Engineering & Biotechnology News 33, no. 6 (March 15, 2013): 08–09. http://dx.doi.org/10.1089/gen.33.6.02.

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39

Ostróżka-Cieślik, Aneta, Barbara Dolińska, and Florian Ryszka. "The Effect of Modified Biolasol Solution on the Efficacy of Storing Isolated Porcine Kidneys." BioMed Research International 2018 (November 12, 2018): 1–7. http://dx.doi.org/10.1155/2018/7465435.

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Biolasol is a newly developed solution for storing the liver, pancreas, kidneys, and heart by simple hypothermia. It exhibits high efficacy in maintaining structural and functional integrity of the graft prior to its transplantation. The solution was modified by the addition of ascorbic acid (0.088g/l) and ascorbic acid with prolactin (1 μg/l PRL + 0.088g/l vitamin C). The effectiveness of the obtained solutions in the protection of nephrons of isolated porcine kidneys was assessed based on the analysis of the activity of ALT (alanine aminotransferase), AST (aspartate aminotransferase), and LDH (lactate dehydrogenase) as well as lactate concentration determined in perfundates collected after 2 h (0′ and 30′ preservation) and 48 h (0′ and 30′ preservation) of graft storage. It has been found that the synergistic action of Biolasol components determines the integrity and stability of cell membranes, which in turn affects the proper functioning of the organ after transplantation. The addition of ascorbic acid and prolactin to Biolasol affects the maintenance of the normal cytoskeleton of the stored graft.

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40

CHAST, ROZ. "Coming Soon from Biolab, Inc." Sciences 34, no. 4 (July 8, 1994): 49. http://dx.doi.org/10.1002/j.2326-1951.1994.tb03778.x.

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41

Liu, Wenjing, Liying Wang, Jin Wang, Jingjing Du, and Chuanyong Jing. "New insights into microbial-mediated synthesis of Au@biolayer nanoparticles." Environmental Science: Nano 5, no. 7 (2018): 1757–63. http://dx.doi.org/10.1039/c8en00104a.

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42

Sivakumar, Sri, Peter R. Diamente, and Frank C. J. M. van Veggel. "Silica-Coated Ln3+-Doped LaF3 Nanoparticles as Robust Down- and Upconverting Biolabels." Chemistry - A European Journal 12, no. 22 (July 24, 2006): 5878–84. http://dx.doi.org/10.1002/chem.200600224.

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43

Brandon, David L., Lisa M. Adams, Lily L. Yang, and Anna M. Korn. "Antibody Interactions withRicinus communisAgglutinins Studied by Biolayer Interferometry." Analytical Letters 47, no. 10 (June 26, 2014): 1747–58. http://dx.doi.org/10.1080/00032719.2014.886693.

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44

Cierpka, L., F. Ryszka, B. Dolińska, Z. Smorąg, R. Słomski, R. Wiaderkiewicz, A. Caban, G. Budziński, G. Oczkowicz, and J. Wieczorek. "Biolasol: Novel Perfusion and Preservation Solution for Kidneys." Transplantation Proceedings 46, no. 8 (October 2014): 2539–41. http://dx.doi.org/10.1016/j.transproceed.2014.09.016.

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45

Wang, Yanqiong, Xi Yang, Chaoyang Gong, Jiangui Mao, Yu Wu, Guolu Yin, Tao Zhu, Gang-Ding Peng, Yun-Jiang Rao, and Yuan Gong. "DC-Biased Optofluidic Biolaser for Uric Acid Detection." Journal of Lightwave Technology 38, no. 6 (March 15, 2020): 1557–63. http://dx.doi.org/10.1109/jlt.2019.2953168.

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46

Ragozin, Elena, Boris Redko, Elena Tuchinsky, Alex Rozovsky, Amnon Albeck, Flavio Grynszpan, and Gary Gellerman. "Biolabile peptidyl delivery systems toward sequential drug release." Biopolymers 106, no. 1 (January 2016): 119–32. http://dx.doi.org/10.1002/bip.22794.

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47

Hawkings, Jon R., Liane G. Benning, Rob Raiswell, Burkhard Kaulich, Tohru Araki, Majid Abyaneh, Anthony Stockdale, Monika Koch-Müller, Jemma L. Wadham, and Martyn Tranter. "Biolabile ferrous iron bearing nanoparticles in glacial sediments." Earth and Planetary Science Letters 493 (July 2018): 92–101. http://dx.doi.org/10.1016/j.epsl.2018.04.022.

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48

Cusano, Angela Maria, Anna Aliberti, Andrea Cusano, and Menotti Ruvo. "Detection of small DNA fragments by biolayer interferometry." Analytical Biochemistry 607 (October 2020): 113898. http://dx.doi.org/10.1016/j.ab.2020.113898.

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49

Zhou, Wei, Shanshan Lin, Rongying Chen, Jun Liu, and Yali Li. "Characterization of antibody-C1q interactions by Biolayer Interferometry." Analytical Biochemistry 549 (May 2018): 143–48. http://dx.doi.org/10.1016/j.ab.2018.03.022.

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50

Zhang, Hao, Wei Li, Hong Luo, Guangming Xiong, and Yuanhua Yu. "Quantitative determination of testosterone levels with biolayer interferometry." Chemico-Biological Interactions 276 (October 2017): 141–48. http://dx.doi.org/10.1016/j.cbi.2017.05.013.

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