2006
DOI: 10.1016/j.cbpc.2005.12.001
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Development of an enzyme-linked immunosorbent assay for vitellogenin of Morelet's crocodile (Crocodylus moreletii)

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Cited by 4 publications
(1 citation statement)
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“…Crude plasma was diluted in Tris-HCl buffer (Tris-HCl, 25 mM, pH 8.1) and placed in a Q-Sepharose fast flow column (size = 25 mL), then eluted with a linear NaCl gradient in Tris-HCl buffer (varying concentrations of NaCl at pH 8.1 included 0.1, 0.2, 0.3, 0.4 and 0.5 M for fractions 1, 2, 3, 4, and 5, respectively). To obtain only protein fractions, salt was eliminated and dialyzed overnight against diethyl-aminoethyl buffer (DEAE) using a dialysis membrane (Spectra/Por 1) (Spectrum, Houston, TX, USA, cut off 250 kDa) [7].…”
Section: Separation Of Protein From Crocodile Plasmamentioning
confidence: 99%
“…Crude plasma was diluted in Tris-HCl buffer (Tris-HCl, 25 mM, pH 8.1) and placed in a Q-Sepharose fast flow column (size = 25 mL), then eluted with a linear NaCl gradient in Tris-HCl buffer (varying concentrations of NaCl at pH 8.1 included 0.1, 0.2, 0.3, 0.4 and 0.5 M for fractions 1, 2, 3, 4, and 5, respectively). To obtain only protein fractions, salt was eliminated and dialyzed overnight against diethyl-aminoethyl buffer (DEAE) using a dialysis membrane (Spectra/Por 1) (Spectrum, Houston, TX, USA, cut off 250 kDa) [7].…”
Section: Separation Of Protein From Crocodile Plasmamentioning
confidence: 99%