Chromatographic separation
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A specific and sensitive LC-MS/MS method has been developed for determination of dapaglifozin (DAP) in human plasma. DAP and the internal standard (empaglifozin) were extracted from human plasma by liquid-liquid extraction.
8p  
 vihyuga
							
 04-03-2025
							
 2
							
 1
							
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Recombinant human kynureninase (L-kynurenine hydrolase, EC 3.7.1.3) was purified to homogeneity (60-fold) from Spodoptera frugiperda (Sf9) cells infected with baculovirus containing the kynureninase gene. The purification protocol comprised ammonium sulfate precipitation and several chromatographic steps, including DEAE–Sepharose CL-6B, hydroxyapatite, strong anionic and cationic separations. The purity of the enzyme was determined by SDS/ PAGE, and the molecular mass verified by MALDI-TOF MS. The monomeric molecular mass of 52.4 kDa determined was 99.99% of the predicted molecular mass.
6p  
 research12
							
 01-06-2013
							
 56
							
 5
							
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The disulfide structure of the CRIPTO/FRL-1/CRYPTIC (CFC) domain of human Cripto protein was determined by a combination of enzymatic and chemical fragmentation, followed by chromatographic separation of the fragments, and characterization by mass spectrometry and N-terminal sequencing. These studies showed that Cys115 forms a disulfide bond with Cys133, Cys128 with Cys149, and Cys131 with Cys140.
9p  
 tumor12
							
 20-04-2013
							
 28
							
 3
							
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The rotor subunitc of the A1AOATP synthase of the hyperthermophilic archaeon Pyrococcus furiosuscontains a conserved Na + -binding motif, indicating that Na + is a coupling ion. To experimentally address the nat-ure of the coupling ion, we isolated the enzyme by detergent solubilization from native membranes followed by chromatographic separation tech-niques.
11p  
 galaxyss3
							
 21-03-2013
							
 47
							
 3
							
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