Syllabus M.Sc. Biochemistry from 2019
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
C9-14 Aliphatic [2-25% Aromatic] Hydrocarbon Solvents Category SIAP
CoCAM 2, 17-19 April 2012 BIAC/ICCA SIDS INITIAL ASSESSMENT PROFILE Chemical C -C Aliphatic [2-25% aromatic] Hydrocarbon Solvents Category Category 9 14 Substance Name CAS Number Stoddard solvent 8052-41-3 Chemical Names Kerosine, petroleum, hydrodesulfurized 64742-81-0 and CAS Naphtha, petroleum, hydrodesulfurized heavy 64742-82-1 Registry Solvent naphtha, petroleum, medium aliphatic 64742-88-7 Numbers Note: Substances in this category are also commonly known as mineral spirits, white spirits, or Stoddard solvent. CAS Number Chemical Description † 8052-41-3 Includes C8 to C14 branched, linear, and cyclic paraffins and aromatics (6 to 18%), <50ppmV benzene † 64742-81-0 Includes C9 to C14 branched, linear, and cyclic paraffins and aromatics (10 to Structural 25%), <100 ppmV benzene Formula † and CAS 64742-82-1 Includes C8 to C13 branched, linear, and cyclic paraffins and aromatics (15 to 25%), <100 ppmV benzene Registry † Numbers 64742-88-7 Includes C8 to C13 branched, linear, and cyclic paraffins and aromatics (14 to 20%), <50 ppmV benzene Individual category member substances are comprised of aliphatic hydrocarbon molecules whose carbon numbers range between C9 and C14; approximately 80% of the aliphatic constituents for a given substance fall within the C9-C14 carbon range and <100 ppmV benzene. In some instances, the carbon range of a test substance is more precisely defined in the test protocol. In these instances, the specific carbon range (e.g. C8-C10, C9-C10, etc.) will be specified in the SIAP. * It should be noted that other substances defined by the same CAS RNs may have boiling ranges outside the range of 143-254° C and that these substances are not covered by the category. -
Metal Ions in Life Sciences"
I N S T R U C T I O N S F O R A U T H O R S Contributing to "Metal Ions in Life Sciences" edited by Astrid Sigel, Helmut Sigel, and Roland K. O. Sigel published by Walter de Gruyter GmbH, Berlin, Germany www.mils-WdG.com (for previous volumes visit www.bioinorganic-chemistry.org/mils) Contents 1. GENERAL REMARKS ............................................................................................... 2 2. SUBMISSION OF THE MANUSCRIPT ................................................................. 2 3. PREPARATION OF THE MANUSCRIPT ............................................................. 3 3.1. Arrangement of the Manuscript .......................................................................... 3 3.2. Organization of the Content of the Manuscript .................................................. 3 3.3. Text .................................................................................................................... 4 3.3.1. General ................................................................................................... 4 3.3.2. Further Directions ................................................................................ 4 3.4. Citations and Reference Style ............................................................................. 4 3.5. Tables ................................................................................................................. 5 3.6. Artwork ............................................................................................................... 5 3.6.1. General -
BULLETIN for the HISTORY of CHEMISTRY Division of the History of Chemistry of the American Chemical Society
BULLETIN FOR THE HISTORY OF CHEMISTRY Division of the History of Chemistry of the American Chemical Society VOLUME 29, Number 1 2004 BULLETIN FOR THE HISTORY OF CHEMISTRY VOLUME 29, CONTENTS NUMBER 1 THE 2003 EDELSTEIN AWARD ADDRESS* MAKING CHEMISTRY POPULAR David Knight, University of Durham, England 1 THE DISCOVERY OF LECITHIN, THE FIRST PHOSPHOLIPID Theodore L. Sourkes, McGill University 9 GABRIEL LIPPMANN AND THE CAPILLARY ELECTROMETER John T. Stock, University of Connecticut 16 KHEMYE: CHEMICAL LITERATURE IN YIDDISH Stephen M. Cohen 21 AN EARLY HISTORY OF CHEMISTRY AT TEXAS TECH UNIVERSITY, 1925-1970* Henry J. Shine, Texas Tech University 30 NOYES LABORATORY, AN ACS NATIONAL CHEMICAL LANDMARK: 100 YEARS OF CHEMISTRY AT THE UNIVERSITY OF ILLINOIS Sharon Bertsch McGrayne 45 BOOK REVIEWS 52 The Cover…….See page 24. Bull. Hist. Chem., VOLUME 29, Number 1 (2004) 1 THE 2003 EDELSTEIN AWARD ADDRESS* MAKING CHEMISTRY POPULAR David Knight, University of Durham, England “Chemistry is wonderful,” wrote evenings, and a bright dawn Linus Pauling (1), “I feel sorry for gleamed over a chemically-based people who don’t know anything society. Intellectually, the science about chemistry. They are miss- did not demand the mathematics re- ing an important source of happi- quired for serious pursuit of the sub- ness.” That is not how the science lime science of astronomy. Chem- has universally been seen in our ists like Joseph Priestley thought it time. We would not expect to see the ideal Baconian science in which lecture-rooms crowded out, chem- everyone might join, for its theoreti- ists as stars to be invited to fash- cal structure was still unformed. -
Personal View – the Evolution of Neurochemistry
Neuroforum 2019; 25(4): 259–264 Review Article Ferdinand Hucho* Personal View – The Evolution of Neurochemistry Two questions – one answer https://doi.org/10.1515/nf-2019-0023 century up to our times. Reductionism was hoped to solve two of the most fundamental riddles which were central to Abstract: This esssay is a personal account of the evolution human thinking since antiquity: The world, believed to be of Neurochemistry in the past century. It describes in par- composed of ‚mind and matter‘, poses the question: What allel the authors way from chemistry to biochemistry and is life? The neurochemist goes one step further and asks: finally to Neurochemistry and the progress of a most ex- what is mind (conciousness, cognition, free will)? The citing chapter of the Life Sciences. It covers the successful physiologist Emil du Bois-Reymond (1818–1896) included time period of reductionist research (by no means compre- these questions in his ‚seven riddles‘ (Finkelstein 2013) hensively), which lay the ground for the recent and future and summarized his answer in 1880 in his famous “igno- systems approach. This development promises answers to ramus et ignorabimus” (“we don‘t know and we never will fundamental questions of our existence as human beings. know”). Never say ‘never’, because this could be the end Keywords: Chemistry; Biochemistry; Life Science; Neuro- of human curiosity and research, preventing discoveries chemistry including new methods of investigation. In the 20th century the question What is life was most vividly posed by physicists like the Nobel laureates Zusammenfassung: Dieser Essay ist ein persönlicher Erwin Schrödinger (Schrödinger 1944; Fischer ed., 1987) Bericht über die Entwicklung der Neurochemie im ver- and Max Delbrück (Delbrück 1986). -
Essays in Neurochemistry and Neuropharmacology Chemical
Volume 89, number 2 FEBS LETTERS May 1978 Essays in Neurochemistry and Neuropharmacology Volume 2 Edited by M. B. H. Youdim, W. Lovenberg, D. F. Sharman and J. R. Lagnado John Wiley and Sons; Chichester, New York, Brisbane, Toronto, 1977 xiv + 174 pages, £8.75 An essay on essays prefaces this book, praising the The Biochemical Society's 'Essays in Biochemistry' literary essay and advocating a comparable form of which antedate the present series by I 1 years are also scientific writing as a leavening or antidote to the despite their name broad, didactically-oriented reviews stereotype of papers proceeding by Methods-Results- in which many authors use figures and tables as a Discussion. The terse wisdom and precise word-choise means of avoiding cumbersome passages of text; a of Bacon, or the charm of Lamb, would indeed be necessary distinction from the literary essay and much welcome in the neurosciences, but this book's to be encouraged. So also are author and subject contents exemplify a different and quite worthy indexes which are lacking in the present book. It also stereotype, the review. Are literary essays ever multi- has no running titles or author's names at the head of author, as are half of the present contributions? Two its pages; and as the list of abbrevations and the of the most effective essays here are indeed single- literature references come at the beginning and end of authored: the first few pages of K. G. Walton's each individual essay, lack of this guidance to where account of cyclic necleotides and postynaptic events the beginning and end are located is to be regretted. -
CHEMISTRY Faculty Douglas A
CHEMISTRY Faculty Douglas A. Fantz, associate professor of chemistry and chair Lilia C. Harvey, interim associate vice president for academic affairs and associate dean of the college and professor of chemistry Ruth E. Riter, professor of chemistry T. Leon Venable, associate professor of chemistry Sarah A. Winget, associate professor of chemistry Agnes Scott’s academic program in chemistry, approved by the American Chemical Society (ACS), introduces students to the principles, applications, and communication of chemical knowledge and provides extensive practical experience with modern instrumentation in laboratory courses and through research opportunities. The science of chemistry concerns the structure and properties of matter with an interest in the changes that occur as matter reacts. The study of chemistry is particularly appropriate to students interested in medicine, academic or industrial scientific research, forensics, or teaching. Two major options (ACS approved or non-ACS approved track) and a minor option are available. The ACS approved major curriculum is most appropriate for students interested in entering industry or continuing their studies in graduate school. The non-ACS approved major curriculum, while rigorous, affords a student flexibility to pursue other academic interests during their time at Agnes Scott. The curriculum for majors requires a strong foundation in all five subdisciplines of chemistry (analytical, inorganic, organic, physical, and biochemistry), while allowing students to tailor upper-level requirements -
Clinical Chemistry Analyzer
Clinical Chemistry Analyzer UMDNS GMDN 16298 Analyzers, Laboratory, Clinical Chemistry, 35918 Laboratory urine analyser IVD, automated Automated 56676 Laboratory multichannel clinical chemistry analyser IVD, automated Other common names: Biochemistry analyzer Health problem addressed Perform tests on whole blood, serum, plasma, or urine samples to determine concentrations of analytes (e.g., cholesterol, electrolytes, glucose, calcium), to provide certain hematology values (e.g., hemoglobin concentrations, prothrombin times), and to assay certain therapeutic drugs (e.g., theophylline), which helps diagnose and treat numerous diseases, including diabetes, cancer, HIV, STD, hepatitis, kidney conditions, fertility, and thyroid problems. Product description Chemistry analyzers can be benchtop devices or placed on a cart; other systems require fl oor space. They are used to determine the concentration of certain metabolites, electrolytes, proteins, and/or drugs in samples of serum, plasma, urine, cerebrospinal fl uid, and/or other body fl uids. Samples are inserted in a slot or loaded onto a tray, and tests are programmed via a keypad or Use and maintenance bar-code scanner. Reagents may be stored within the analyzer, User(s): Laboratory technician and it may require a water supply to wash internal parts. Results Maintenance: Laboratory technician; are displayed on a screen, and typically there are ports to biomedical or clinical engineer connect to a printer and/or computer. Training: Initial training by manufacturer and Core medical equipment - Information Principles of operation manuals After the tray is loaded with samples, a pipette aspirates a precisely measured aliquot of sample and discharges it into the Environment of use reaction vessel; a measured volume of diluent rinses the pipette. -
Analysis of the Trends in Biochemical Research Using Latent Dirichlet Allocation (LDA)
Article Analysis of the Trends in Biochemical Research Using Latent Dirichlet Allocation (LDA) Hee Jay Kang 1, Changhee Kim 1,* and Kyungtae Kang 2,* 1 College of Business Administration, Incheon National University, 119, Academy-ro, Yeonsu-gu, Incheon 22012, Korea; [email protected] 2 Department of Applied Chemistry, Kyung Hee University, 1732, Deogyeong-daero, Giheung-gu, Yongin-si, Gyeonggi-do 130-701, Korea * Correspondence: [email protected] (C.K.); [email protected] (K.K.); Tel.: +82-2-880-8594(C.K.) Received: 15 April 2019; Accepted: 13 June 2019; Published: 18 June 2019 Abstract: Biochemistry has been broadly defined as “chemistry of molecules included or related to living systems”, but is becoming increasingly hard to be distinguished from other related fields. Targets of its studies evolve rapidly; some newly emerge, disappear, combine, or resurface themselves with a fresh viewpoint. Methodologies for biochemistry have been extremely diversified, thanks particularly to those adopted from molecular biology, synthetic chemistry, and biophysics. Therefore, this paper adopts topic modeling, a text mining technique, to identify the research topics in the field of biochemistry over the past twenty years and quantitatively analyze the changes in its trends. The results of the topic modeling analysis obtained through this study will provide a helpful tool for researchers, journal editors, publishers, and funding agencies to understand the connections among the diverse sub-fields in biochemical research and even see how the research topics branch out and integrate with other fields. Keywords: biochemistry; topic modeling; research trend; LDA 1. Introduction Biochemistry is the study of the structure, composition, and chemical reactions of substances in living systems and includes the sciences of molecular biology, immunochemistry, and neurochemistry, as well as bioinorganic, bioorganic, and biophysical chemistry [1]. -
Neurochemical Mechanisms Underlying Alcohol Withdrawal
Neurochemical Mechanisms Underlying Alcohol Withdrawal John Littleton, MD, Ph.D. More than 50 years ago, C.K. Himmelsbach first suggested that physiological mechanisms responsible for maintaining a stable state of equilibrium (i.e., homeostasis) in the patient’s body and brain are responsible for drug tolerance and the drug withdrawal syndrome. In the latter case, he suggested that the absence of the drug leaves these same homeostatic mechanisms exposed, leading to the withdrawal syndrome. This theory provides the framework for a majority of neurochemical investigations of the adaptations that occur in alcohol dependence and how these adaptations may precipitate withdrawal. This article examines the Himmelsbach theory and its application to alcohol withdrawal; reviews the animal models being used to study withdrawal; and looks at the postulated neuroadaptations in three systems—the gamma-aminobutyric acid (GABA) neurotransmitter system, the glutamate neurotransmitter system, and the calcium channel system that regulates various processes inside neurons. The role of these neuroadaptations in withdrawal and the clinical implications of this research also are considered. KEY WORDS: AOD withdrawal syndrome; neurochemistry; biochemical mechanism; AOD tolerance; brain; homeostasis; biological AOD dependence; biological AOD use; disorder theory; biological adaptation; animal model; GABA receptors; glutamate receptors; calcium channel; proteins; detoxification; brain damage; disease severity; AODD (alcohol and other drug dependence) relapse; literature review uring the past 25 years research- science models used to study with- of the reasons why advances in basic ers have made rapid progress drawal neurochemistry as well as a research have not yet been translated Din understanding the chemi- reluctance on the part of clinicians to into therapeutic gains and suggests cal activities that occur in the nervous consider new treatments. -
Bioenergetics Unbelievable
HISTORICAL PERSPECTIVES Bioenergetics Unbelievable ... ... but true! MARS - The easiest Data Analysis for Microplate Readers. Key features that the MARS software can do: Standard curve calculation wizard Linear, 4-parameter, cubic-spline, segmental curve fits Enzyme kinetics - Michaelis-Menten, Lineweaver-Burk, Scatchard Automatic DNA / RNA concentration determination 3D well scanning for cell-based assays Delta F% calculation for HTRF® Z’ calculation User-defined formula generator FDA 21 CFR Part 11 compliant Overlay plot of esterase catalysed pNPA Multi-user software license included reactions at different concentrations. Find our microplate readers on www.bmglabtech.com FLUOstar PHERAstar FS NOVOstar NEPHELOstar Stacker HTRF is a registered trademark of Cisbio International. The Journal of Biological Chemistry TABLE OF CONTENTS 2010 HISTORICAL PERSPECTIVES ON BIOENERGETICS PROLOGUE REFLECTIONS H1 JBC Historical Perspectives: Bioenergetics. Nicole Kresge, Robert H13 A Research Journey with ATP Synthase. Paul D. Boyer D. Simoni, and Robert L. Hill H30 Happily at Work. Henry Lardy CLASSICS H41 Keilin, Cytochrome, and the Respiratory Chain. E. C. Slater H2 Polyribonucleotide Synthesis and Bacterial Amino Acid Uptake: the Work of Leon A. Heppel H48 Reminiscences of Leon A. Heppel. Leon A. Heppel H5 Unraveling the Enzymology of Oxidative Phosphorylation: the Work of Efraim Racker H8 Ion Transport in the Sarcoplasmic Reticulum: the Work of David H. MacLennan H10 ATP Synthesis and the Binding Change Mechanism: the Work of Paul D. Boyer JOURNAL OF BIOLOGICAL CHEMISTRY i PROLOGUE This paper is available online at www.jbc.org © 2010 by The American Society for Biochemistry and Molecular Biology, Inc. Printed in the U.S.A. JBC Historical Perspectives: Bioenergetics* Nicole Kresge, Robert D. -
Are Enzymes Accurate Indicators of Postmortem Interval?: a Biochemical Analysis Karly Laine Buras Louisiana State University and Agricultural and Mechanical College
Louisiana State University LSU Digital Commons LSU Master's Theses Graduate School 2006 Are enzymes accurate indicators of postmortem interval?: a biochemical analysis Karly Laine Buras Louisiana State University and Agricultural and Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_theses Part of the Social and Behavioral Sciences Commons Recommended Citation Buras, Karly Laine, "Are enzymes accurate indicators of postmortem interval?: a biochemical analysis" (2006). LSU Master's Theses. 177. https://digitalcommons.lsu.edu/gradschool_theses/177 This Thesis is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Master's Theses by an authorized graduate school editor of LSU Digital Commons. For more information, please contact [email protected]. ARE ENZYMES ACCURATE INDICATORS OF POSTMORTEM INTERVAL? A BIOCHEMICAL ANALYSIS A Thesis Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Master of Arts in The Department of Geography and Anthropology by Karly Laine Buras B.S., Louisiana State University, 2001 May 2006 ACKNOWLEDGEMENTS I would like to thank the members of my thesis committee for their continued encouragement and help throughout my program. My heartfelt thanks go out to Bob Tague, Mary Manhein, and Grover Waldrop for helping me along the way. I would especially like to thank Grover Waldrop for his contributions to my thesis expenses, as well as for the use of his lab for my research. I would not have been able to do any of this without his help. -
Department of Chemistry and Biochemistry
Non-thesis option, 33 hours minimum, including: 30 Department of Chemistry Independent study 3 and Biochemistry Total Hours 33 Up to 15 hours may be taken in related courses given by other Web Site: http://www.odu.edu/chemistry (http://www.odu.edu/chemistry/) departments pending approval from the Graduate Studies Committee of the Department of Chemistry and Biochemistry. At least 60 percent of the credit 110 Alfriend Chemistry Building hours must be from 600-level courses or higher. Norfolk, VA 23529-0126 (757) 683-4078 Students who earn a grade of less than a B- in any two graduate courses will not be allowed to continue in the M.S. program. John B. Cooper, Chair John Donat, Graduate Program Director Core Courses Overview There are six core areas. These are: The Department of Chemistry and Biochemistry strives to provide high • analytical chemistry, quality of education in Chemistry and Biochemistry for both graduate and • biochemistry, undergraduate students and to engage in scholarly research at the forefront in • environmental chemistry, both the fields of chemistry and biochemistry. The department's variety of • inorganic chemistry, research programs provide with a high quality, broad based education, which • organic chemistry, and not only prepares graduates for successful careers, it also prepares graduates for a lifetime of learning. In addition to offering the Master of Science • physical chemistry. program and Doctor of Philosophy program in Chemistry, the Department of Students enrolled in the research/thesis option must take one course from Chemistry and Biochemistry also partners with the Graduate School to offer three different core areas; non-thesis option students must take one course an interdisciplinary Ph.D.