Results 231 to 240 of about 1,050,605 (265)
Some of the next articles are maybe not open access.
Comparison of Blocking Agents for an Elisa for Lps
Journal of Immunoassay, 2000ELISA is a sensitive, specific, reproducible and fast method for detection of antigen-antibody reactions. In case of non-protein antigens as LPS, problems exist, such as poor proportion of coating to microplates, non-specific binding of antibodies to the plastic wells.
Z, Péterfi, B, Kocsis
openaire +2 more sources
Aujeszky's disease: Blocking ELISA for the detection of serum antibodies
Journal of Virological Methods, 1986A blocking ELISA for the detection of serum antibodies to Aujeszky's disease virus has been developed. The test was designed in particular with a view to examining large numbers of blood samples. It has been found to be sensitive, specific and precise.
K J, Sørensen, J C, Lei
openaire +2 more sources
Effective Blocking and Stabilizing Methods Using Synthetic Polymer on ELISA
2023In ELISA, blocking reagents and stabilizers are important to improve the sensitivity and/or quantitative nature of the measurement system. Usually, biological substances such as bovine serum albumin and casein are used, but they still have problems such as lot-to-lot differences and biohazard.
Tomozumi, Noda +4 more
openaire +2 more sources
Journal of Immunological Methods, 1989
The effect of blocking and non-blocking was compared in ELISA, immunostaining dot-blots and western blots using phosphate-buffered saline with and without the addition of Tween 20 for washes and dilutions. The results indicated that when Tween 20 was included in phosphate-buffered saline, a blocking agent and a blocking step were not required in ...
K, Mohammad, A, Esen
openaire +2 more sources
The effect of blocking and non-blocking was compared in ELISA, immunostaining dot-blots and western blots using phosphate-buffered saline with and without the addition of Tween 20 for washes and dilutions. The results indicated that when Tween 20 was included in phosphate-buffered saline, a blocking agent and a blocking step were not required in ...
K, Mohammad, A, Esen
openaire +2 more sources
A monoclonal blocking-ELISA for detection of orthopoxvirus antibodies in feline sera
Veterinary Microbiology, 1996A double sandwich blocking-ELISA using a genus-specific neutralizing monoclonal antibody (MAb) against the vaccinia virus 32 kD adsorption protein (D8L open reading frame: ORF) was developed to detect orthopoxvirus (OPV) antibodies in sera. A collection of 2173 feline serum samples was examined in an epidemiological study.
C P, Czerny +4 more
openaire +2 more sources
Development of a blocking ELISA for Caprine parainfluenza virus type 3
Journal of Virological Methods, 2017Caprine parainfluenza virus type 3 (CPIV3) is a novel pathogen mainly causing respiratory diseases in goats. At present, there are no high throughput and rapid testing methods available for epidemiological investigation. In this study, we designed a modified method for selection of hybridomas that secrete monoclonal antibodies (mAb) specific for CPIV3.
Li, Mao +8 more
openaire +2 more sources
A monoclonal antibody blocking enzyme-linked immunosorbent assay (B-ELISA) was developed to detect antibodies to Mycoplasma bovis in cattle sera. The assay was highly specific and sensitive and there was no cross-reaction detected. This method revealed a
Robert G Hirst
exaly +2 more sources
Development and evaluation of a blocking ELISA for serological diagnosis of equine infectious anemia
Applied Microbiology and Biotechnology, 2023Equine infectious anemia (EIA) is an important viral disease characterized by persistent infection in equids worldwide. Most EIA cases are life-long virus carriers with low antibody reactions and without the appearance of clinical symptoms. A serological test with high sensitivity and specificity is required to detect inapparent infection.
Zhe Hu +14 more
openaire +2 more sources
A monoclonal blocking ELISA detecting serum antibodies to Mycoplasma hyopneumoniae
Veterinary Microbiology, 1992A monoclonal blocking enzyme-linked immunosorbent assay (ELISA) for detection of antibodies to Mycoplasma hyopneumoniae in porcine serum has been developed. The monoclonal antibody (mAb) reacts with an M. hyopneumoniae specific epitope on a molecule of approximately 74 kDa. Only sera from M. hyopneumoniae infected pigs were able to block the binding of
N C, Feld +4 more
openaire +2 more sources
Veterinary Microbiology, 1992
A blocking (B) dot enzyme-linked immunosorbent assay (ELISA), using a monoclonal antibody (mAb) against a group specific antigen of bluetongue virus (BTV) is described for the detection of BTV antibodies to BTV in cattle sera. Dots of BTV antigens were adsorbed to nitrocellulose (NC) strips and/or NC mounted in the windows of dipsticks.
A, Afshar, G C, Dulac, J, Riva
openaire +2 more sources
A blocking (B) dot enzyme-linked immunosorbent assay (ELISA), using a monoclonal antibody (mAb) against a group specific antigen of bluetongue virus (BTV) is described for the detection of BTV antibodies to BTV in cattle sera. Dots of BTV antigens were adsorbed to nitrocellulose (NC) strips and/or NC mounted in the windows of dipsticks.
A, Afshar, G C, Dulac, J, Riva
openaire +2 more sources

