<p>The PAGE had a resolving gel of 7% in pH 6.5 HEPES−Imidazole buffer and a stacking gel of 4% in pH 5.4 Bis-tris−Acetic acid buffer; the Tricine−Bis-tris electrode buffers in pH 6.3 were employed as anode and cathode solutions. (a) the bands in natural colors, (b) the bands of native state in grey scale without red filter, (c) the bands of native state in grey scale with red filter and (d) the bands in fluorescence under UV-light at 365 nm. The R-PC and AP sample used in the PAGE was the R-PC fraction from the ion exchange chromatography.</p
Micrographs of selected samples at 80x magnification and Extract Ion Chromatograms (EICs) obtained b...
<p>(a) The phycobiliprotein extract; (b) the R-PE fraction from the gel filtration on Sepharose CL-4...
<p>The SDS-PAGE was performed with a gradient separating gel of 13%-17% (w/v) in pH 9.2 Tris-HCl buf...
<p>The PAGE with the resolving gel of 9% in pH 6.5 and the stacking gel of 4% in pH 5.4 was performe...
<p>(A) the Tris−Gly PAGE with a resolving gel of 6.5% in pH 8.8 Tris−HCl buffer, a staking gel of 3%...
<p>The PAGE with the stacking gel of 4% in pH 6.0 Bis-tris−HEPES−Acetic acid buffer was performed re...
<p>The PAGE was carried out with a resolving gel of 9% in pH 6.5 Bis-tris−HEPES−MES buffer and with ...
<p>The absorption (solid line) and fluorescence (dot line) spectra of the prepared R-PCs and APs sho...
<p>The PAGE had a 6.5% (w/v) separation gel in the neutral buffer system and the IEF had 5.5% (w/v) ...
<p>(A) Bis-tris−HEPES−MES buffer systems; (B) HEPES−Imidazole/Bis-tris buffer systems; (C) Imidazole...
<p>(A) Bis-tris−HEPES−MES buffer systems; (B) HEPES−Imidazole/Bis-tris buffer systems; (C) Imidazole...
<p>Lane 1 and 2 in a pH range from 4.0 to 6.5 and lane 3 and 4 in a pH range from 3.0 to 10.0. The p...
<p>(A) Purification of rhLY by cation-exchange chromatography through the Hiscreen SP FF prepacked c...
<p>The native-PAGE of the purified R-PE (lane 1) and the R-PC (lane 2) purified by the ion exchange ...
Protein A chromatography has been a popular method for purification of therapeutic monoclonal antibo...
Micrographs of selected samples at 80x magnification and Extract Ion Chromatograms (EICs) obtained b...
<p>(a) The phycobiliprotein extract; (b) the R-PE fraction from the gel filtration on Sepharose CL-4...
<p>The SDS-PAGE was performed with a gradient separating gel of 13%-17% (w/v) in pH 9.2 Tris-HCl buf...
<p>The PAGE with the resolving gel of 9% in pH 6.5 and the stacking gel of 4% in pH 5.4 was performe...
<p>(A) the Tris−Gly PAGE with a resolving gel of 6.5% in pH 8.8 Tris−HCl buffer, a staking gel of 3%...
<p>The PAGE with the stacking gel of 4% in pH 6.0 Bis-tris−HEPES−Acetic acid buffer was performed re...
<p>The PAGE was carried out with a resolving gel of 9% in pH 6.5 Bis-tris−HEPES−MES buffer and with ...
<p>The absorption (solid line) and fluorescence (dot line) spectra of the prepared R-PCs and APs sho...
<p>The PAGE had a 6.5% (w/v) separation gel in the neutral buffer system and the IEF had 5.5% (w/v) ...
<p>(A) Bis-tris−HEPES−MES buffer systems; (B) HEPES−Imidazole/Bis-tris buffer systems; (C) Imidazole...
<p>(A) Bis-tris−HEPES−MES buffer systems; (B) HEPES−Imidazole/Bis-tris buffer systems; (C) Imidazole...
<p>Lane 1 and 2 in a pH range from 4.0 to 6.5 and lane 3 and 4 in a pH range from 3.0 to 10.0. The p...
<p>(A) Purification of rhLY by cation-exchange chromatography through the Hiscreen SP FF prepacked c...
<p>The native-PAGE of the purified R-PE (lane 1) and the R-PC (lane 2) purified by the ion exchange ...
Protein A chromatography has been a popular method for purification of therapeutic monoclonal antibo...
Micrographs of selected samples at 80x magnification and Extract Ion Chromatograms (EICs) obtained b...
<p>(a) The phycobiliprotein extract; (b) the R-PE fraction from the gel filtration on Sepharose CL-4...
<p>The SDS-PAGE was performed with a gradient separating gel of 13%-17% (w/v) in pH 9.2 Tris-HCl buf...