Analyze Diet

Topic:Laboratory Methods

Laboratory methods in equine research encompass a variety of techniques and procedures used to analyze biological samples from horses to study health, disease, genetics, and physiology. These methods include hematological analyses, biochemical assays, molecular biology techniques, and microbiological cultures. Commonly utilized laboratory techniques involve blood tests for complete blood count (CBC) and serum chemistry, polymerase chain reaction (PCR) for genetic and infectious disease studies, and enzyme-linked immunosorbent assays (ELISA) for detecting specific proteins or antibodies. These methods provide valuable data that contribute to understanding equine health and disease mechanisms. This page compiles peer-reviewed research studies and scholarly articles that explore the application, development, and outcomes of laboratory methods in the context of equine research.
Regulation of the immune response. IV. Antibody-mediated suppression of the immune response to haptens and heterologous erythrocyte antigens in vitro.
Journal of immunology (Baltimore, Md. : 1950)    October 1, 1973   Volume 111, Issue 4 1228-1235 
Kappler JW, van der Hoven A, Dharmarajan U, Hoffmann M.No abstract available
The characterisation of an equine adenovirus.
Australian veterinary journal    October 1, 1973   Volume 49, Issue 10 456-459 doi: 10.1111/j.1751-0813.1973.tb09291.x
Wilks CR, Studdert MJ.No abstract available
Studies on the substrate specificity of acylneuraminate cytidylyltransferase and sialytransferase of submandibular glands from cow, pig and horse.
Hoppe-Seyler's Zeitschrift fur physiologische Chemie    October 1, 1973   Volume 354, Issue 10-11 1405-1414 doi: 10.1515/bchm2.1973.354.2.1405
Schauer R, Wember M.No abstract available
Equine herpesviruses: antigenic relationships and deoxyribonucleic acid densities.
Infection and immunity    October 1, 1973   Volume 8, Issue 4 621-627 doi: 10.1128/iai.8.4.621-627.1973
Plummer G, Goodheart CR, Studdert MJ.Equine herpesviruses with a deoxyribonucleic acid density of 1.716 to 1.717 g/cm(3) were compared with one another by the plaque-reduction test and by the rate of development of cytopathic effect as indicated by plaque size in rabbit kidney cultures. Of the 19 isolates studied, the 9 which had already been tentatively labeled equine abortion viruses were serologically similar to one another; each of them grew more quickly than did any of the other 10 isolates although the mean plaque sizes formed a series of gradations with no clear hiatus which would permit the unequivocal delineation of the ...
[Afferent spinal fibres in the equine brain stem. An experimental study using the silver impregnation method].
Zentralblatt fur Veterinarmedizin. Reihe C: Anatomie, Histologie, Embryologie    September 1, 1973   Volume 2, Issue 3 209-220 
Karamanlidis AN.No abstract available
Preparation of equine infectious anemia antigens for diagnosis.
Japanese journal of microbiology    September 1, 1973   Volume 17, Issue 5 393-399 doi: 10.1111/j.1348-0421.1973.tb00790.x
Ueda S, Samejima T, Kuroda S, Nakamura J.No abstract available
Application of inductively-coupled plasma excitation sources to the determination of trace metals in microliter volumes of biological fluids.
Clinical chemistry    August 1, 1973   Volume 19, Issue 8 807-812 
Kniseley RN, Fassel VA, Butler CC.No abstract available
[Purification and properties of L-cysteinsulfinic decarboxylase from horse kidneys].
Bollettino della Societa italiana di biologia sperimentale    July 15, 1973   Volume 49, Issue 11 679-685 
Federici G, Santoro L, Tomati U, Cannella C.No abstract available
The equilibrium unfolding parameters of horse and sperm whale myoglobin. Effects of guanidine hydrochloride, urea, and acid.
The Journal of biological chemistry    July 10, 1973   Volume 248, Issue 13 4623-4634 
Puett D.No abstract available
Cytotoxicity for erythroblasts in horse antihuman thymocyte -globulin.
Transplantation    July 1, 1973   Volume 16, Issue 1 70-73 doi: 10.1097/00007890-197307000-00017
Krantz SB.No abstract available
Plasma protein binding of digitoxin and digoxin in several mammalian species.
Research in veterinary science    July 1, 1973   Volume 15, Issue 1 81-87 
Baggot JD, Davis LE.No abstract available
Studies with normal erythrocytes of the English Thoroughbred horse.
Equine veterinary journal    July 1, 1973   Volume 5, Issue 3 135-136 doi: 10.1111/j.2042-3306.1973.tb03212.x
Allen BV, Archer RK.No abstract available
[Experience in the preparation and use of inactivated antigens from influenza viruses of different origins].
Voprosy virusologii    July 1, 1973   Volume 18, Issue 4 489-493 
Isachenko VA, Sokolova NN, Shestochenko MA, Zakstel'skaia LIa.No abstract available
[Fractionation of blood group substance B from the gastric mucosa of the horse].
Biokhimiia (Moscow, Russia)    July 1, 1973   Volume 38, Issue 4 723-726 
Likhosherstov LM, Arbatskiĭ NP, Derevitskaia VA.No abstract available
Analytical scanning isoelectrofocusing.
Annals of the New York Academy of Sciences    June 15, 1973   Volume 209 65-79 doi: 10.1111/j.1749-6632.1973.tb47519.x
Catsimpoolas N.No abstract available
Determination of serum total iron-binding capacity.
Journal of clinical pathology    June 1, 1973   Volume 26, Issue 6 457 doi: 10.1136/jcp.26.6.457-a
Betts CA, Stuart B.No abstract available
Characteristics of the in vitro stimulation of horse leucocytes by phytohemagglutinin and antigen.
Zeitschrift fur Immunitatsforschung, experimentelle und klinische Immunologie    June 1, 1973   Volume 145, Issue 4 364-375 
Lazàry S, de Weck AL, Gerber H, Schatzmann U, Straub R.No abstract available
Reduction of ferricytochrome c by dithionite ion: electron transfer by parallel adjacent and remote pathways.
Proceedings of the National Academy of Sciences of the United States of America    June 1, 1973   Volume 70, Issue 6 1701-1703 doi: 10.1073/pnas.70.6.1701
Creutz C, Sutin N.The kinetics of the reduction of horseheart ferricytochrome c by sodium dithionite (phosphate buffer-sodium chloride; pH 6.5, mu = 1.0, 25 degrees ) features two reaction pathways; one with the rate constant k(3) = 1.17 x 10(4) M(-1) sec(-1), the other with the rate constant k(1)k(2)/k(-1) = 6.0 x 10(4) M(-1) sec(-1). These pathways are interpreted in terms of remote attack (possibly by way of the exposed edge of the porphyrin system) and adjacent attack (requiring the opening of the heme crevice). The limiting rate for the adjacent pathway (k(1) = 30 sec(-1)) is in good agreement with the rat...
Interaction of ascorbic acid and metallothionein-like fractions from equine renal cortex.
Archives internationales de physiologie et de biochimie    May 1, 1973   Volume 81, Issue 2 385 
Roosemont JL.No abstract available
Circulating concentrations of luteinizing hormone during estrous cycle of mares as determined by radioimmunoassay.
American journal of veterinary research    May 1, 1973   Volume 34, Issue 5 631-636 
Whitmore HL, Wentworth BC, Ginther OJ.No abstract available
Formation of steroids by the pregnant mare. IV. Metabolism of 14 C-mevalonic acid and 3 H-dehydroisoandrosterone injected into the fetal circulation.
Endocrinology    May 1, 1973   Volume 92, Issue 5 1397-1404 doi: 10.1210/endo-92-5-1397
Bhavnani BR, Short RV.No abstract available
Physical properties and subunit structure of butyrylcholinesterase from horse serum.
Biochemistry    April 10, 1973   Volume 12, Issue 8 1622-1630 doi: 10.1021/bi00732a025
Lee JC, Harpst JA.No abstract available
[Mineral and trace element content of equine serum and plasma].
DTW. Deutsche tierarztliche Wochenschrift    April 1, 1973   Volume 80, Issue 7 166 
Meyer H, Lemmer U.No abstract available
A comparison of three laboratory tests for pregnancy diagnosis in the mare.
Equine veterinary journal    April 1, 1973   Volume 5, Issue 2 94-95 doi: 10.1111/j.2042-3306.1973.tb03202.x
McCaughey WJ, Hanna J, O'Brien JJ.No abstract available
Equine infectious anemia: sensitivity of the agar-gel immunodiffusion test, and the direct and the indirect complement-fixation tests for the detection of antibodies in equine serum.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    April 1, 1973   Volume 37, Issue 2 171-176 
Carrier SP, Boulanger P, Bannister GL.The comparative values of the direct, the indirect complement-fixation and the agar-gel immunodiffusion tests were assessed for the diagnosis of equine infectious anemia. Antibodies were detected on the agar-gel immunodiffusion test as early as 18 days post-inoculation in the serums of experimentally infected horses and were readily detectable in all the subsequent bleedings. Complement-fixing antibodies, demonstrable by the direct method, were detected commencing about the same time. However, these were not long-lasting and were replaced by the non-complement-fixing antibodies demonstrable by...
Radioimmunoassay for equine luteinizing hormone.
Journal of reproduction and fertility    March 1, 1973   Volume 32, Issue 3 475-477 doi: 10.1530/jrf.0.0320475
Anand AS, Thompson KW, Wentworth BC, First NL.No abstract available
Tropical horse tick: effects of solvents on oviposition.
Journal of economic entomology    February 1, 1973   Volume 66, Issue 1 125-127 doi: 10.1093/jee/66.1.125
Beadles ML, Drummond RO, Whetstone TM.No abstract available
[A study of aggregating immunoglobulins in horses (“AI” or IgB or IgI)].
Annales d'immunologie    February 1, 1973   Volume 124, Issue 1 45-74 
Lavergne M, Raynaud M.No abstract available
Species differences in luteinizing hormone as inferred from slope variations in a radioligand receptor assay.
Endocrinology    February 1, 1973   Volume 92, Issue 2 646-649 doi: 10.1210/endo-92-2-646
Leidenberger F, Reichert LE.No abstract available
Extraction of equine infectious anemia immunodiffusion antigen with the aid of the chaotropic agent, thiocyanate.
Applied microbiology    February 1, 1973   Volume 25, Issue 2 190-194 doi: 10.1128/am.25.2.190-194.1973
Hart LT, Broussard EA.Immunodiffusion antigen from spleens of horses infected with equine infectious anemia virus was prepared by methods employing freeze-thaw cycles and thiocyanate treatment. Thiocyanate (0.5 M) permitted the recovery of the greatest amount of antigen. Furthermore, it was most effective for recovery of immunodiffusion antigen from spleens which yielded unsatisfactory concentrations of antigen by the conventional freeze-thaw or water-extraction methods. The reactivity of the antigen did not appear to be affected by this chemical treatment.