1995
DOI: 10.1016/0300-9629(95)00077-k
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Interconversions of lipophorin particles by adipokinetic hormone in hemolymph of Panstrongylus megistus, Dipetalogaster maximus and Triatoma infestans (Hemiptera: Reduviidae)

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Cited by 25 publications
(24 citation statements)
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“…Protein concentration was determined by Bradford assay (1976). Lipophorin titer was assayed by indirect ELISA assay, using an antiserum against purified lipophorin from P. megistus (Canavoso & Rubiolo 1995.…”
Section: Chemicals -mentioning
confidence: 99%
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“…Protein concentration was determined by Bradford assay (1976). Lipophorin titer was assayed by indirect ELISA assay, using an antiserum against purified lipophorin from P. megistus (Canavoso & Rubiolo 1995.…”
Section: Chemicals -mentioning
confidence: 99%
“…However, no changes in the hemolymph carbohydrate in insects flown for a short time were observed. On another hand, by employing fat bodies from starved triatomine bugs, we previously reported that AKH promoted generation of LDLp, the lipoprotein responsible for the delivery of lipids during flight (Canavoso & Rubiolo 1995).…”
mentioning
confidence: 99%
“…Lipophorin standard -A standard curve for measurement of HDLp by ELISA was carried out employing HDLp from D. maximus, isolated from hemolymph by KBr density gradient ultracentrifugation and dialysed overnight against phosphate buffered saline (PBS) at pH 7.4 (Canavoso & Rubiolo 1995). The concentration of lipophorin standard was quantified by Bradford (1976).…”
Section: Determination Of Lipophorin Hdlpmentioning
confidence: 99%
“…Serum anti-lipophorin HDLp from adults of D. maximus, obtained in rabbits as described previously (Canavoso & Rubiolo 1995), was diluted in PBS-Tween (1:10.000) containing 0.1% bovine serum albumin and loaded into each well incubating for 60 min at 37 o C. Plates were washed and loaded with anti-rabbit inmunoglobulin conjugated to horseradish peroxidase (Sigma) in PBS-Tween and incubated for 30 min at 37 o C. Then, the plates were washed again and developed at 37 o C for 30 min with o-phenylenediamine in substrate buffer (81.5 mM sodium phosphate, 33.3 mM citric acid; 0.08% hydrogen peroxide, pH 5.0) and read at 490 nm.…”
Section: Determination Of Lipophorin Hdlpmentioning
confidence: 99%
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