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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 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
Clinical Pathology of Liver Disease in Horses.
The Veterinary clinics of North America. Equine practice    October 13, 2026   doi: pii: S0749-0739(26)00017-9. 10.1016/j.cveq.2026.04.002
Liver disease in horses is primarily evaluated using the routine serum biochemical profile with a few additional specialty tests of liver function that are performed when indicated. Serum enzyme activities are evaluated to indicate hepatocellular damage and cholestasis. Liver function is evaluated using synthetic markers like BUN, albumin, bilirubin, and clotting times, while clearance function tests such as serum bile acids and ammonia are performed separately. Most equine liver disease is characterized by some degree of hepatocellular damage and cholestasis, while decreased liver function is...
[Development of PCR methods for detection of EAV infection].
   October 13, 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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