2012
DOI: 10.1504/tbj.2012.050197
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Monoclonal antibodies and reagents for botulinum research

Abstract: Botulinum neurotoxin (BoNT) is produced by Clostridium botulinum as a dichain protein of ~ 150 kDa that blocks acetylcholine release resulting in muscular paralysis. Diagnosis of BoNT often relies on the mouse bioassay that has a detection limit of 10-20 pg/mL and can take up to four days to complete. Rapid in vitro methods for toxin detection are needed and to date, most rely on either immunoassay or endopeptidase activity. In the latter, many also use specific antibodies to concentrate the toxin. We have dev… Show more

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Cited by 2 publications
(4 citation statements)
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“…A combination (1:1:1) of biotinylated mAbs F1-40, F1-41 and F2-43 each at 1 μg/mL gave the best detection sensitivities for BoNT/A compared to single or a sets of two mAbs. 19 For BoNT/B detection, mAb MCS6-27 was used as the capture mAb and biotinylated mAb BoB92-32 was used the detector mAb. Only a single mAb was available for BoNT/B detection at this time.…”
Section: Resultsmentioning
confidence: 99%
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“…A combination (1:1:1) of biotinylated mAbs F1-40, F1-41 and F2-43 each at 1 μg/mL gave the best detection sensitivities for BoNT/A compared to single or a sets of two mAbs. 19 For BoNT/B detection, mAb MCS6-27 was used as the capture mAb and biotinylated mAb BoB92-32 was used the detector mAb. Only a single mAb was available for BoNT/B detection at this time.…”
Section: Resultsmentioning
confidence: 99%
“…To simulate the effect of polyclonal antibodies, we tested the use of a mixture of mAbs as detector antibodies. A combination (1:1:1) of biotinylated mAbs F1-40, F1-51, and F2-43 each at 1 μg/mL gave the best detection sensitivities for BoNT/A as compared to single or a sets of two mAbs . For BoNT/B detection, mAb MCS6-27 was used as the capture mAb, and biotinylated mAb BoB92-32 was used the detector mAb.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Sensitive and reliable immunoassay platforms could be ideally used for detecting the presence of toxin antigens in in food samples for surveillance purpose or in clinical specimens alongside clinical diagnosis, to substantially reduce false negative or inconclusive results obtained from clinical specimens. Unlike the MLB, which relies on sample dilution (Stanker and Cheng, 2012 ), immunoassays have an excellent dynamic range of quantification (Worbs et al, 2015 ). Immunoassays are more cost effective, requiring fewer dedicated personnel, less instrumentation and are not skill intensive (Lindstrom and Korkeala, 2006 ; Cai et al, 2007 ; Capek and Dickerson, 2010 ).…”
Section: In Vitro Methods For Detection Of Bonts and Neurotomentioning
confidence: 99%