Relevant bibliographies by topics / Hormone immunoassays

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Hormone immunoassays'

Author: Grafiati
Published: 5 June 2025
Last updated: 16 July 2025

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Journal articles on the topic "Hormone immunoassays"

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Sokoll, Lori J., Frank H. Wians, and Alan T. Remaley. "Rapid Intraoperative Immunoassay of Parathyroid Hormone and Other Hormones: A New Paradigm for Point-of-Care Testing." Clinical Chemistry 50, no. 7 (2004): 1126–35. http://dx.doi.org/10.1373/clinchem.2003.030817.

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Abstract Background: The first description of the use of a rapid assay for the measurement of intact parathyroid hormone (PTH) in patients undergoing parathyroidectomy for hyperparathyroidism was reported in 1988. Subsequent improvements in the analytical performance of the rapid intraoperative PTH assay allowed the establishment of its clinical utility in the surgical management of hyperparathyroidism. These modifications also allowed the assay to be performed in or near the operating suite. Methods: We searched MEDLINE, using the following key words: intraoperative, rapid, quick, parathyroid
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Welsh, Kerry J., and Steven J. Soldin. "DIAGNOSIS OF ENDOCRINE DISEASE: How reliable are free thyroid and total T3 hormone assays?" European Journal of Endocrinology 175, no. 6 (2016): R255—R263. http://dx.doi.org/10.1530/eje-16-0193.

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Hypothyroidism is a very common disorder worldwide, for which the usual treatment is monotherapy with levothyroxine (L-T4). However, a number of patients treated with L-T4 continue to report symptoms of hypothyroidism despite seemingly normal levels of thyroid-stimulating hormone (TSH), free-T3 (FT3) and free-T4 (FT4) measured by immunoassay. This review summarizes the limitations of the immunoassays commonly used to measure thyroid hormone levels and emphasizes the advantages of the role of liquid chromatography-tandem mass spectrometry (LC-MS/MS). Immunoassays for free thyroid hormone are af
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Dewey, Hannah, Jacob Thompson, Matthew Fisher, and Januka Budhathoki-Uprety. "(Nanocarbons Division Poster Award, Third Place) Development of an Optical Probe for the Detection of Steroid Hormones." ECS Meeting Abstracts MA2024-01, no. 8 (2024): 827. http://dx.doi.org/10.1149/ma2024-018827mtgabs.

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Hormones play major roles in several biological processes. Steroid hormones are crucial for reproductive maturation in women. Abnormal steroid hormones (e.g., estrogen) levels have several pathological conditions, including ovarian failure, bone loss, or increased risk for breast cancer. Thus, accurate and precise detection of steroid hormone levels is crucial for timely health interventions. The current gold standard for steroid hormone detection is immunoassays. Optical measurement technologies are promising alternatives to traditional immunoassays. Optical tools could provide a novel platfo
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Braunstein, Glenn D. "Spurious Serum Hormone Immunoassay Results: Causes, Recognition, Management." European Endocrinology 18, no. 2 (2022): 141. http://dx.doi.org/10.17925/ee.2022.18.2.141.

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For over 50 years, immunoassays have been extensively used to quantitate hormones in blood, other fluids and tissues. Each assay has its own sensitivity, specificity and other analytical components. Despite the differences between commercial products, these assays provide important clinical information about hormone levels in patients. However, inaccurate results can occur because of technical issues, as well as patient-specific factors that can interfere with immunoassay hormone measurements. The latter include excessive normal blood or serum components, the presence of cross-reacting substan
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Kato, Hajime, Naoko Hidaka, Minae Koga, et al. "Altered Thyroid Function Tests Observed in Hypophosphatasia Patients Treated with Asfotase Alfa." International Journal of Endocrinology 2021 (October 28, 2021): 1–5. http://dx.doi.org/10.1155/2021/5492267.

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Background. Asfotase alfa is the only approved treatment that can normalize mineralization in patients with hypophosphatasia (HPP). Its interference in alkaline phosphatase (ALP) dependent immunoassays has been reported. Objective. To describe thyroid function tests interfered with by asfotase alfa and elucidate the underlying mechanism. Patients and Methods. Three patients with HPP treated with asfotase alfa were included. Thyroid hormone levels measured using five different immunoassays with or without ALP as a labeling enzyme during asfotase alfa treatment were evaluated. Results. After the
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Klee, George G. "Interferences in hormone immunoassays." Clinics in Laboratory Medicine 24, no. 1 (2004): 1–18. http://dx.doi.org/10.1016/j.cll.2004.01.003.

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Debeljak, Željko, Ivana Marković, Vatroslav Šerić, et al. "Analytical bias of automated immunoassays for six serum steroid hormones assessed by LC-MS/MS." Biochemia medica 30, no. 3 (2020): 422–31. http://dx.doi.org/10.11613/bm.2020.030701.

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Introduction: There is a growing amount of evidence showing the significant analytical bias of steroid hormone immunoassays, but large number of available immunoassays makes conduction of a single comprehensive study of this issue hardly feasible. Aim of this study was to assess the analytical bias of six heterogeneous immunoassays for serum aldosterone, cortisol, dehydroepiandrosterone sulphate (DHEAS), testosterone, 17-hydroxyprogesterone (OHP) and progesterone using the liquid chromatography coupled to the tandem mass spectrometry (LC-MS/MS). Materials and methods: This method comparison st
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Strilić, David, Bojan Stanimirov, and Maja Đanić. "Biotin interference with laboratory test results." Hospital Pharmacology - International Multidisciplinary Journal 11, no. 3 (2024): 1509–28. https://doi.org/10.5937/hpimj2403509s.

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Introduction: Biotin interference in laboratory tests is a growing concern, particularly due to the widespread use of biotin not only as a therapeutic agent but also as a supplement in the cosmetic industry. Immunoassays utilizing biotin-streptavidin technology are especially susceptible to interference, which can result in inaccurate test results, misdiagnosis, and inappropriate treatment. Methodology: This review synthesizes information from scientific literature available through databases like PubMed and Google Scholar. Keywords such as "biotin", "interference" and "immunoassay" were used
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Seth, John. "Standardization of Protein Hormone Immunoassays." Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 33, no. 6 (1996): 482–85. http://dx.doi.org/10.1177/000456329603300602.

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Strathmann, Frederick G., Grace Borlee, Donald E. Born, Luis F. Gonzalez-Cuyar, Bertrand R. Huber, and Geoffrey S. Baird. "Multiplex Immunoassays of Peptide Hormones Extracted from Formalin-Fixed, Paraffin-Embedded Tissue Accurately Subclassify Pituitary Adenomas." Clinical Chemistry 58, no. 2 (2012): 366–74. http://dx.doi.org/10.1373/clinchem.2011.170613.

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Abstract BACKGROUND The current gold standard for diagnostic classification of many solid-tissue neoplasms is immunohistochemistry (IHC) performed on formalin-fixed, paraffin-embedded (FFPE) tissue. Although IHC is commonly used, there remain important issues related to preanalytic variability, nonstandard methods, and operator bias that may contribute to clinically significant error. To increase the quantitative accuracy and reliability of FFPE tissue–based diagnosis, we sought to develop a clinical proteomic method to characterize protein expression in pathologic tissue samples rapidly and q
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Dissertations / Theses on the topic "Hormone immunoassays"

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Rauf, Femina. "Chimeric and Recombinant Protein Reagents for Cellular Analysis and Immunoassays." Diss., The University of Arizona, 2011. http://hdl.handle.net/10150/145441.

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Development of chimeric, recombinant peptides, proteins and enzymes expands the availability of protein/enzyme–based tools for cellular analysis and new assay platforms. Ideal protein reagents for cellular analysis must translocate into a variety of cells with minimum cell damage, retain stability and biological activity within the cell during analysis, and provide a reliable, measurable signal. This work focused on development, characterization and utilization of chimeric recombinant peptide, protein and enzyme reagents for cellular analysis and immunoassays. A cell-penetrating, fluorescent p
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Casagrande, Alessandra. "Importância dos ensaios para medida do hormônio de crescimento na determinação da atividade da acromegalia." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2005. http://hdl.handle.net/10183/7598.

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A dosagem do GH no soro é essencial para confirmar ou excluir o seu excesso. Na acromegalia, a ausência de critérios clínicos suficientemente sensíveis para monitorizar o sucesso do tratamento faz com que o GH sérico seja o procedimento de escolha e, para isso, é essencial que a sua dosagem seja realizada de forma confiável, capaz de permitir interpretações uniformes. Vários critérios hormonais têm sido propostos para caracterizar remissão da acromegalia, incluindo níveis séricos de GH randômico inferior a 2,5 μg/l, nadir de GH durante o teste de tolerância oral a glicose inferior a 1,0 μg/l e
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El, Fighi Abdul Baset Abdussalam M. "Studies on the immunoassay of human growth hormone in urine." Thesis, University of Salford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244870.

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Evans, Lee W. "The development of immunoassays for follistatin and activin and their clinical applications." Thesis, University of Reading, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.389532.

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Ritter, Nina. "Detection of Anti-hGH Antibodies in Serum Samples of Children Treated with RhGH." Doctoral thesis, Universitätsbibliothek Leipzig, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-97443.

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The present study deals with the comparison and establishment of methods for the detection of antibodies against recombinant human growth hormone (rhGH). Therefore, different methods for the detection of hGH-Abs were evaluated and compared in order to establish a test system that can be used for the detection of neutralizing antibodies against hGH, which could be developed under rhGH treatment. This manuscript describes in detail the validation of a newly developed biological assay, the neutralizing hGH-antibody assay (NAb assay). Therefore, a cell line transfected with the growth hormone rece
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Maioli, Marcos Antonio [UNESP]. "Quantificação do fator de crescimento semelhante a insulina I (IGF-I) em plasma bovino por ELISA." Universidade Estadual Paulista (UNESP), 2016. http://hdl.handle.net/11449/134284.

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Submitted by MARCOS ANTONIO MAIOLI null (maioli_marcos@hotmail.com) on 2016-02-17T13:03:36Z No. of bitstreams: 1 Tese Maioli, M.A..pdf: 2279252 bytes, checksum: 484c7c928f7a1a221c494bcff9e436b0 (MD5)<br>Approved for entry into archive by Juliano Benedito Ferreira (julianoferreira@reitoria.unesp.br) on 2016-02-17T16:54:14Z (GMT) No. of bitstreams: 1 maioli_ma_dr_araca.pdf: 2279252 bytes, checksum: 484c7c928f7a1a221c494bcff9e436b0 (MD5)<br>Made available in DSpace on 2016-02-17T16:54:14Z (GMT). No. of bitstreams: 1 maioli_ma_dr_araca.pdf: 2279252 bytes, checksum: 484c7c928f7a1a221c494bcff9e4
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Maioli, Marcos Antonio. "Quantificação do fator de crescimento semelhante a insulina I (IGF-I) em plasma bovino por ELISA /." Araçatuba, 2016. http://hdl.handle.net/11449/134284.

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Orientador: Guilherme de Paula Nogueira<br>Banca: Marcelo Vasconcelo Meireles<br>Banca: Daniel de Jesus Cardoso de Oliveira<br>Banca: Andréa Fontes Garcia<br>Resumo: Esse estudo teve como objetivo a padronização de um ensaio imunoenzimático (ELISA) para a determinação das concentrações plasmáticas de IGF-I total, utilizando o sistema de amplificação biotina-estreptavidina peroxidase em um ensaio competitivo. O IGF-I foi extraído da IGFBP, utilizando o tampão glicina acidificado seguido de neutralização do pH com hidróxido de sódio. As microplacas foram sensibilizadas com anti IgG de coelho, e
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Ramchandra, Desai Suchita. "Development of an immunoassay panel to predict aseptic implant loosening." Thesis, Högskolan i Skövde, Institutionen för biovetenskap, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-16285.

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During our lifetime, our bones constantly go through remodelling to maintain the skeletal system. This is done by osteoblasts that deposit new bone tissue, osteoclasts that remove the bone matrix and mechanosensing osteocytes. In case of bone implants, increased resorption by osteoclasts due to inflammation (inflammatory osteolysis) leads to aseptic implant loosening. This study focuses on how to detect these inflammatory resorbing cells at an early stage and prevent their activity with appropriate medication. To achieve this, we differentiated classical monocytes into macrophage-like cells, o
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Dowd, Peter Dylan. "The photophysical characterisation of a fluorescence-based immunoassay for the detection of gonadotropin-releasing hormone, type-1 (GnRH-I)." Thesis, University of Strathclyde, 2013. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=24378.

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The homogeneous assay format has been identified as having the potential to make an effective impact in the field of 'point-of-care or near patient testing. Homogeneous assays have the advantage that, by eliminating the need for multiple preparation steps, they can be rapid and easy to use in comparison with most solid-phase assay formats. However homogeneous assays tend to be generally less sensitive than their heterogeneous counterparts, giving results that are qualitative or at best semi-quantitative. This work presents a 'model' fluorescence-based homogeneous immunoassay for the detection
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Polegato, Bruna Furlan. "Determinação dos perfis de estrógenos e progestinas fecais durante o ciclo estral, gestação e período pós-parto em cervos-do-pantanal (Blastocerus dichotomus) em cativeiro /." Jaboticabal : [s.n.], 2008. http://hdl.handle.net/11449/98204.

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Orientador: José Maurício Barbanti Duarte<br>Banca: Paulo Henrique Franceschini<br>Banca: Claudio Alvarenga de Oliveira<br>Resumo: Atualmente, o conhecimento sobre a fisiologia e a biologia reprodutiva de cervos-do-pantanal (Blastocerus dichotomus) é escasso e as lacunas existentes aumentam a vulnerabilidade da espécie à extinção. Neste contexto, os objetivos deste trabalho foram: (1) caracterizar alguns parâmetros relacionados à fisiologia reprodutiva de fêmeas de cervos-do-pantanal e (2) fornecer métodos adequados para o acesso às diferentes fases do ciclo reprodutivo. Para isso, seis fêmeas
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Books on the topic "Hormone immunoassays"

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Pankatz, Anja. Monoklonale Antikörper gegen equines Follikelstimulierendes Hormon: Herstellung und Einsatz im Immunoassay. [s.n.], 1998.

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Bartkowski, Sonja. Monoklonale Antikörper gegen equines Luteinisierendes Hormon/Choriongonadotropin und deren Einsatz im Immunoassay. [s.n.], 1999.

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Florence, Haseltine, and Albertson Barry D, eds. Non-radiometric assays: Technology and application in polypeptide and steroid hormone detection : proceedings of a meeting held in Bethesda, Maryland, October 15-16, 1987. Liss, 1988.

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Lamb, Edmund J., and Finlay MacKenzie. Analytical aspects of measurements and laboratory values in kidney disease. Edited by David J. Goldsmith. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0104.

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This chapter explains the essential principles that must underlie meaningful laboratory data in terms of the production of an accurate result and an intelligent interpretation of its significance. These principles are illustrated by reference to three measurements that nephrologists commonly request: serum creatinine (Jaffe to creatinase); urinary albumin and total protein (Lowry and tetrabromphenol blue to immunoassay); and parathyroid hormone (first to third generation immunoassays). These analytes are placed in their historical and clinical context, and the progress that has been made, and
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Staff, CIBA Foundation Symposium. Ciba Foundation Symposium - Immunoassay of Hormones. Wiley & Sons, Limited, John, 2008.

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Wolstenholme, G. E. W., and Margaret P. Cameron. Immunoassay of Hormones, Volume 14: Colloquia on Endocrinology. Wiley & Sons, Incorporated, John, 2009.

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Young, Hugh. Immunoassay Kit Directory: Part 1 Peptide Hormones June 1994. Springer London, Limited, 2012.

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Non-radiometric assays: Technology and applications in polypeptide and steroid hormone detection ; proceedings of a meeting held in Bethesda, Maryland, Oct. 15-16, 1988. A. Liss, 1988.

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Hormone assays in biological fluids. Humana Press, 2006.

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Non-invasive monitoring of stoat reproductive hormones. Science & Technical Publishing, Dept. of Conservation, 2007.

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Book chapters on the topic "Hormone immunoassays"

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Khripach, V. A., V. N. Zhabinskii, and R. P. Litvinovskaya. "Immunoassays of brassinosteroids." In Brassinosteroids: A Class of Plant Hormone. Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-94-007-0189-2_14.

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Xu, Chuanlai, Hua Kuang, and Liguang Xu. "β-Agonist and Hormone Immunoassays in Food." In Food Immunoassay. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9034-0_5.

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Sturgeon, Catharine. "External Quality Assessment Schemes for Immunoassays." In Hormone Assays in Biological Fluids. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-616-0_19.

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Weiler, E. W. "Plant Hormone Immunoassays Based on Monoclonal and Polyclonal Antibodies." In Immunology in Plant Sciences. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82853-9_1.

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Seth, John. "Luteinizing Hormone." In The Immunoassay Kit Directory. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1414-1_35.

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Seth, John. "Parathyroid Hormone." In The Immunoassay Kit Directory. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1414-1_47.

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Seth, John. "Adrenocorticotrophic Hormone." In The Immunoassay Kit Directory. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1414-1_1.

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Seth, John. "Growth Hormone." In The Immunoassay Kit Directory. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1414-1_25.

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Wheeler, Michael J. "Immunoassay Techniques." In Hormone Assays in Biological Fluids. Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-986-9:1.

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Wheeler, Michael J. "Immunoassay Techniques." In Hormone Assays in Biological Fluids. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-616-0_2.

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Conference papers on the topic "Hormone immunoassays"

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Hamad, Eyad M., Ghadeer Hawamdeh, Noor Abu Jarrad, Omar Yasin, Samer I. Al-Gharabli, and Raed Shadfan. "Detection of Human Chorionic Gonadotropin (hCG) Hormone using Digital Lateral Flow Immunoassay." In 2018 40th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2018. http://dx.doi.org/10.1109/embc.2018.8513355.

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Abosaber, Nourah S. "THE IMPACT OF SMOKING ON MALE REPRODUCTIVE HORMONE LEVELS AND INFERTILITY IN JEDDAH." In Dubai International Conference on Research in Life-Science & Healthcare, 22-23 February 2024. Global Research & Development Services, 2024. http://dx.doi.org/10.20319/icrlsh.2024.2829.

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Tobacco use is overgrowing in all Arab countries and is one of the greatest threats to current and future global health. The negative effect of tobacco use on sperm quality has been examined in numerous studies. In Saudi Arabia, especially in Jeddah, this systematic research aims to investigate the impact of smoking on the hormonal profile in 75 men between the ages of 19 and 60 years who were randomly selected between smokers, infertile and nonsmokers from patients visiting King Abdulaziz University Medical Services Center and Health plus fertility &amp; woman’s health center in Jeddah, SA. C
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"TOWARDS A NEW HOMOGENEOUS IMMUNOASSAY FOR GONADOTROPIN-RELEASING HORMONE BASED ON TIME-RESOLVED FLUORESCENCE ANISOTROPY." In International Conference on Biomedical Electronics and Devices. SciTePress - Science and and Technology Publications, 2011. http://dx.doi.org/10.5220/0003152001840188.

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Kirch-heimer, J. C., H. Kölbl, G. Christ, and G. Tatra. "CHANGES IN FIBRINOLYTIC PARAMETERS AFTER DELIVERY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644843.

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Recent studies by Astedt et al. have shown increasing levels of plasminogen activator inhibitor during pregnancy, but the origin of the inhibitor is unknown. Levels of fibrinolytic parameters were determined in plasma collected from 18 females (age 22.7 ± 3.2, mean ± SD) after a normal medically controlled pregnancy at the time of delivery and on the following 5 days. Tissue-type plasminogen activator (tPA) antigen was measured by enzyme immunoassay, urokinase type plasminogen activator (uPA) antigen by a radioimmunoassay and plasminogen activator inhibitor (PAI ) by a functional assay. The re
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Ozaki, Bianca Chames, Paulo Cesar Zimmermann Felchner, Tatiane Mendes Boutin Bartneck Telles, et al. "Thyroid-stimulating hormone reference intervals in the first trimester in an iodine-sufficient population of pregnant women attended by the public health system in Curitiba, South of Brazil." In Resumos do 56º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2024. https://doi.org/10.5327/1516-3180.142s1.11154.

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Objective: Thyroid disorders are prevalent among women of reproductive age. Serum thyroid-stimulating hormone (TSH) concentration is the primary marker used to assess thyroid function during pregnancy. Changes in thyroid function during pregnancy can significantly affect a woman’s health, pregnancy outcomes, fetal health, and child development. When comparing TSH levels between pregnant and non-pregnant women, TSH levels are generally lower during pregnancy, particularly in the first trimester, with gradual increase during pregnancy. Therefore, this study aimed to determine the normal referenc
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Reports on the topic "Hormone immunoassays"

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พงษ์เลาหพันธุ์, ศุภวิวัธน์, та ธีรพงศ์ ยะทา. การพัฒนาพาหะนำส่งยีนเหนี่ยวนำการตายของเซลล์แบบอะพอพโทซิสระดับนาโน เพื่อการคุมกำเนิดสัตว์เพศผู้แบบไม่ผ่าตัดทำหมัน : ต้นแบบเพื่อการคุมจำนวนประชากรสุนัขและแมวจรจัด. คณะสัตวแพทยศาสตร์ จุฬาลงกรณ์มหาวิทยาลัย, 2019. https://doi.org/10.58837/chula.res.2019.42.

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การศึกษาวิจัยนี้มีวัตถุประสงค์ เพื่อตรวจสอบการนำไปใช้ของอนุภาคไคโตซานระดับนาโนที่ถูกดัดแปลงให้มีคุณสมบัติเป็นตัวนำส่งยีนเหนี่ยวนำการตายแบบอะพอพโทซิสเข้าสู่เซลล์อัณฑะที่มีตัวรับฮอร์โมนโกนาโดโทรปินรีลิสซิ่ง โดยการออกแบบตัวนำส่งยีนนี้สามารถนำไปใช้ประโยชน์ในการทำหมันสัตว์เพศผู้แบบไม่ผ่าตัด การศึกษานี้ได้มีการรายงานผลของอนุภาคไคโตซานระดับนาโนเชื่อมติดกับฮอร์โมนโกนาโดโทรปินรีลิสซิ่ง (Gonadotropin Releasing Hormone-modified Chitosan; GnRH-CS) เพื่อนำส่งยีนอย่างมีเป้าหมาย และการใช้เปปไทด์โกนาโดโทรปินรีลิสซิ่งในการระบุเป้าหมายการนำส่งยีนไปสู่เซลล์ที่มีตัวรับฮอร์โมนโกนาโดโทรปินรีลิสซิ่ง (GnRH receptor;
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2

Delwiche, Michael, Boaz Zion, Robert BonDurant, Judith Rishpon, Ephraim Maltz, and Miriam Rosenberg. Biosensors for On-Line Measurement of Reproductive Hormones and Milk Proteins to Improve Dairy Herd Management. United States Department of Agriculture, 2001. http://dx.doi.org/10.32747/2001.7573998.bard.

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The original objectives of this research project were to: (1) develop immunoassays, photometric sensors, and electrochemical sensors for real-time measurement of progesterone and estradiol in milk, (2) develop biosensors for measurement of caseins in milk, and (3) integrate and adapt these sensor technologies to create an automated electronic sensing system for operation in dairy parlors during milking. The overall direction of research was not changed, although the work was expanded to include other milk components such as urea and lactose. A second generation biosensor for on-line measuremen
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