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.
The Electrophoresis of the Blood Platelets of the Horse with Reference to Their Origin and to Thrombus Formation.
The Journal of experimental medicine    April 30, 1928   Volume 47, Issue 5 677-683 doi: 10.1084/jem.47.5.677
Abramson HA.1. The cataphoretic velocity of blood platelets (horse) in plasma has been found to be between 40 and 51 micro per sec. per volt per cm. The mean velocity obtained from five horses is . 45 micro per sec. per volt per cm. 2. The cataphoretic velocity of polymorphonuclear leucocytes in similar specimens is practically identical with that of the platelets. This is noteworthy because of the fact that lymphocytes and red cells have different speeds. 3. With spontaneous agglutination of platelets, white cells and red cells, there is no change in the cataphoretic velocity incidental to aggregation. 4...
The Precipitin Reaction of Antipneumococcus Sera: II. The Ratio of Precipitin to Protective Antibody.
The Journal of experimental medicine    January 1, 1928   Volume 47, Issue 1 79-89 doi: 10.1084/jem.47.1.79
Friedlander M, Sobotka H, Banzhaf EJ.The precipitin indices for a number of monovalent and polyvalent antipneumococcus sera were determined under known conditions, and found to vary as did the number of protective units. The ratio precipitin index/protective units in monovalent sera was found to lie between 2.8 and 4.8 for Type I and to be about ten times greater for Type III. Lower values were found in polyvalent horses and when mixing heterologous monovalent sera with each other. The influence of the duration of treatment upon the quotient was studied. Several refined and concentrated preparations showed a relative increase in ...
The Occurrence of Degraded Pneumococci in Vivo.
The Journal of experimental medicine    April 30, 1927   Volume 45, Issue 5 807-814 doi: 10.1084/jem.45.5.807
Reimann HA.It is conceivable that a change from the virulent, non-phagocytable S form of Pneumococcus to the avirulent phagocytable R form may take place in pneumococcus disease, but the experiments here reported do not settle the question whether or not this is an important factor in determining the outcome in natural infection. It has been shown experimentally that the degradation from the S form to the R form actually does take place in cultures of Pneumococcus growing in agar subcutaneously embedded in guinea pigs, in agar enclosed in vials subcutaneously embedded in rabbits, and spontaneously in the...
A Specific Flocculation Reaction Occurring Between Alcoholic Extracts of Pneumococci and Antipneumococcus Serum.
The Journal of experimental medicine    January 31, 1927   Volume 45, Issue 2 227-241 doi: 10.1084/jem.45.2.227
Jungeblut CW.1. A flocculation reaction has been described which occurs between alcoholic extracts of pneumococci and antipneumococcus serum. 2. The reaction appears to be species-specific. It is not strictly type-specific, as slight or moderate cross-reactions occurred between Type I serums and Type II and Type III extracts. 3. The flocculating power of the serum from five horses undergoing immunization with pneumococcus, Type I, did not develop to any extent before the end of the 4th or 5th month. 4. In the case of two of these horses in which it was possible to carry out parallel tests on a larger numbe...
STANDARDIZATION OF ANTIMENINGOCOCCIC SERUM.
The Journal of experimental medicine    November 30, 1918   Volume 28, Issue 6 779-790 doi: 10.1084/jem.28.6.779
Amoss HL, Marsh P.Experiments were made for the purpose of testing the reaction of protection against infection as a measure of potency of antimeningococcic serum. The results of the experiments were extremely variable and bore no relation to the quality of the sera as determined by the period of immunization of the horses from which they were obtained, or the indications of efficiency based upon their employment in human cases of epidemic meningitis. The results also failed entirely to conform to the agglutination titer of the sera tested and to be affected by the different type forms of the meningococci. We r...
A Note on the Production of Antipneumococcus Sera.
The Journal of experimental medicine    May 1, 1917   Volume 25, Issue 5 629-632 doi: 10.1084/jem.25.5.629
Wadsworth AB, Kirkbride MB.Horses immunized to Type I pneumococci developed serum, 0.1 cc. of which protected against 0.5 cc. of a virulent culture, 0.000001 cc. of which killed mice in less than 40 hours. Protective tests of serum from horses immunized to Type II organisms varied, 0.1 cc. protecting, however, in certain instances against 0.1 and 0.01 cc. of virulent homologous culture. Types I and II sera obtained in our experiments with culture sediment and whole culture did not vary markedly for a given type and corresponded closely in their protective titer with samples of sera received from The Rockefeller Institut...
Serum-Globulin and Diphtheric Antitoxin: A Comparative Study of the Amount of Globulin in Normal and Antitoxic Sera, and the Relation of the Globulins to the Antitoxic Bodies.
The Journal of experimental medicine    October 1, 1900   Volume 5, Issue 1 47-66 doi: 10.1084/jem.5.1.47
Hiss PH, Atkinson JP.THE RESULTS OF THE FOREGOING EXPERIMENTS MAY BE BRIEFLY SUMMARIZED AS FOLLOWS: The amount of antitoxic substance obtained by precipitation with magnesium sulphate from the blood-serum of the horse corresponds, as nearly as can be determined by the use of test guinea-pigs, in full to the protective power of the serum from which it is obtained, i. e. the precipitate from 1 cc. of serum will protect against the same amount of toxin as 1 cc. of the serum itself. Equal amounts of the precipitates by magnesium sulphate from immunized and non-immunized horses act differently toward toxin; i. e. the p...
The Fractional Precipitation of the Globulin and Albumin of Normal Horse’s Serum and Diphtheria Antitoxic Serum, and the Antitoxic Strength of the Precipitates.
The Journal of experimental medicine    October 1, 1900   Volume 5, Issue 1 67-76 doi: 10.1084/jem.5.1.67
Atkinson JP.1. The globulins of both normal and diphtheria antitoxic serum exhibit chemically toward reagents the same reactions, being precipitated by magnesium sulphate and split up into fractions in precisely the same way. 2. All of the diphtheric antitoxic power of both normal and immunized serum is always carried by the globulin and its fractional precipitates. 3. During the fractional precipitation of the serum globulin of horses immunized from diphtheria toxin and horses not immunized from diphtheria toxin, some of the globulin is lost, likewise at the same time some of the antitoxic power of the g...
The Use of Mallein for the Diagnosis of Glanders in Horses and Experiments with an Albumose Extracted from Cultures of the Bacillus Malleus.
The Journal of comparative medicine and veterinary archives    November 1, 1892   Volume 13, Issue 11 643-657 
De Schweinitz EA, Kilborne FL.No abstract available
[Development of PCR methods for detection of EAV infection].
   March 21, 2026  
The goal of this work was the development of suitable (real-time) RT-PCR techniques for fast and sensitive diagnosis of EAV and for molecular-epidemiological characterisation of viral strains, as an alternative to virus isolation. To this purpose two conventional RT-PCR methods and one real-time RT-PCR were adapted to detect the broadest possible spectrum of viral strains. Several dilutions with Bucyrus strain showed a 100-fold higher sensitivity of real-time RT-PCR and heminested RT-PCR compared to simple RT-PCR. Making use of 11 cell culture supernatants of different EAV isolates and 7 semen...
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