2015
DOI: 10.1016/j.biologicals.2015.03.003
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Quantitative single dilution liquid phase blocking ELISA for sero-monitoring of foot-and-mouth disease in India

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Cited by 8 publications
(14 citation statements)
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“…These strains were used in the vaccine formulation. Antibody titres were quantified by SdLPBE as described previously (Sharma et al., ). In brief, test serum samples were diluted to 1 : 32 and mixed individually with equal volume of pre‐titrated inactivated whole virus antigen of the three serotypes making the final dilution of serum to 1 : 64.…”
Section: Methodsmentioning
confidence: 99%
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“…These strains were used in the vaccine formulation. Antibody titres were quantified by SdLPBE as described previously (Sharma et al., ). In brief, test serum samples were diluted to 1 : 32 and mixed individually with equal volume of pre‐titrated inactivated whole virus antigen of the three serotypes making the final dilution of serum to 1 : 64.…”
Section: Methodsmentioning
confidence: 99%
“…Proficiency in estimating the antibody titres by various state level diagnostic laboratories was determined as described previously (Sharma et al., ). About 10% of the total samples tested at AICRP laboratories were selected at random and re‐tested at the central laboratory, Mukteswar.…”
Section: Methodsmentioning
confidence: 99%
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“…To overcome this problem, a single-dilution LPB-ELISA was previously developed to measure the FMDV-specific antibody titer in serum. This method is based on a linear regression curve generated with reference standards to extrapolate the antibody titers of the sera tested (72,73).…”
Section: Enzyme-linked Immunosorbent Assaymentioning
confidence: 99%
“…Secondly, how to accurately differentiate FMDV infected from immunized animals is an important challenge. Normally, the serological methods for FMDV antibody level evaluation are all based on SPs and whole virus, including virus neutralization test, 10 liquid phase blocking enzyme linked immunosorbent assay (LPB-ELISA), 11 solid-phase competition ELISA (SPCE), 12 while ELISAs based on NSPs are normally used to discriminate infected animals from vaccinated animals. [13][14][15][16] Recently, the immunochromatographic strip was be successfully used in various elds due to its specicity, sensitivity, rapidity, low cost and adaptability for eld detection and high sample throughput.…”
Section: Introductionmentioning
confidence: 99%