1997
DOI: 10.1006/abio.1997.2144
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Characterization of Antibody 444 Using Chromatographically Purified Enantiomers of Juvenile Hormones I, II, and III: Implications for Radioimmunoassays

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Cited by 20 publications
(12 citation statements)
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“…The antiserum was raised in rabbits to 10R JH III, and has been shown to recognize JH from tobacco hornworm (Goodman et al, 1995;Cusson et al, 1997) and honeybee (Guidulgi et al, 2005) with high sensitivity by radioimmunoassay. Western blotting was performed on hemolymph proteins that were transferred to nitrocellulose membranes (Bio-Rad) after one-dimensional separation by 8% SDS-PAGE.…”
Section: Page and Immunological Proceduresmentioning
confidence: 99%
“…The antiserum was raised in rabbits to 10R JH III, and has been shown to recognize JH from tobacco hornworm (Goodman et al, 1995;Cusson et al, 1997) and honeybee (Guidulgi et al, 2005) with high sensitivity by radioimmunoassay. Western blotting was performed on hemolymph proteins that were transferred to nitrocellulose membranes (Bio-Rad) after one-dimensional separation by 8% SDS-PAGE.…”
Section: Page and Immunological Proceduresmentioning
confidence: 99%
“…The antiserum was raised in rabbits to 10R JH III and has been shown to recognize JH from tobacco hornworm (Goodman et al, 1995;Cusson et al, 1997) and honeybee (Guidulgi et al, 2005) with high sensitivity by radioimmunoassay. The antibody is also useful for identification of JH that is covalently bound to denatured proteins (Zhou et al, 2006b).…”
Section: Western Blottingmentioning
confidence: 99%
“…Racemic [10-3 H]JH I, II, and III were enantiomerically purified separately (7). Baseline separation of (10R,11S) natural enantiomer (fast eluting) and (10S,11R) unnatural enantiomer (slower eluting) was achieved for racemic [10-3 H]JH I and II using a Haskel pump connected to a Chiralpak AS "guard" column (4.6 ϫ 50 mm) eluted at 0.5 ml/min.…”
Section: [10-3 H] Jh and Jh Diol Enantiomeric Purificationmentioning
confidence: 99%
“…Subsequently, this group (6) devised a shorter (7-step) synthesis of (10R)- [12-3 H]JH III starting from methyl farnesoate, again in a 97:3 mix of enantiomers, using the Sharpless asymmetric epoxidation. Cusson et al (7) presented an attractive method of totally resolving enantiomers of JH I-III by chiral chromatography, utilizing nonlabeled forms of the JH to study binding specificities of an antibody to JH.…”
mentioning
confidence: 99%
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