First investigation of polyoxoniobate and polyoxotantalate aqueous speciation by capillary zone electrophoresis

RSC Advances ◽  
2015 ◽  
Vol 5 (79) ◽  
pp. 64119-64124 ◽  
Author(s):  
Gauthier J.-P. Deblonde ◽  
Nathalie Delaunay ◽  
Dahye Lee ◽  
Alexandre Chagnes ◽  
Gérard Cote ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Capillary Zone Electrophoresis ◽  
Zone Electrophoresis ◽  
Capillary Zone ◽  
First Time

Aqueous solutions of hexaniobate (HxNb6O19x−8, 0 ≤ x ≤ 3) and hexatantalate ions (HxTa6O19x−8, 0 ≤ x ≤ 3) have been probed by capillary zone electrophoresis (CE) for the first time.

Study of properties of silicone-silica crystalline nanospheres in aqueous solutions by capillary zone electrophoresis

2010 ◽  
Vol 3 (1) ◽  
pp. 65 ◽  
Author(s):  
N.G. Vanifatova ◽  
B.Y. Spivakov ◽  
A.I. Belogorokhov ◽  
Y.A. Karpov ◽  
Ilya Kuselman
Keyword(s):  
Aqueous Solutions ◽  
Capillary Zone Electrophoresis ◽  
Zone Electrophoresis ◽  
Capillary Zone

Determination of pKa Values of Diclofenac and Ibuprofen in Aqueous Solutions by Capillary Zone Electrophoresis

2019 ◽  
Vol 29 (1) ◽  
pp. 443-448 ◽  
Author(s):  
Alicia G. Vicenteno-Vera ◽  
Tania Campos-Hernandez ◽  
Maria T. Ramirez-Silva ◽  
Annia Galano ◽  
Alberto Rojas-Hernandez
Keyword(s):  
Aqueous Solutions ◽  
Capillary Zone Electrophoresis ◽  
Pka Values ◽  
Zone Electrophoresis ◽  
Capillary Zone

scholarly journals Hemoglobin Ottawa (HBA2:c.46G>C) and β+ thalassemia (HBB:c.-138C>T) detected in an Indian male by capillary zone electrophoresis

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Beverley M. Pullon ◽  
Jordyn A. Moore
Keyword(s):  
Capillary Zone Electrophoresis ◽  
Indian Population ◽  
Transcriptional Factors ◽  
Red Cell ◽  
Zone Electrophoresis ◽  
Red Cell Indices ◽  
Capillary Zone ◽  
First Time ◽  
Indian Male ◽  
Thalassemia Mutation

Hemoglobin (Hb) Ottawa [α15(A13)Gly>Arg], also known as Hb Siam, results from GGT>CGT mutation in codon 15 of either HBA1 or HBA2. Hb Ottawa carriers typically have normal hematology but when the variant is coinherited with either α or β thalassemia, microcytic red cell indices were observed. The percentage of variant detected using routine methodology was variable (14-33%), with a higher percentage found when co-inherited with an abnormal α-globin genotype. The case presented here involved an Indian male with microcytic red cell indices, who was heterozygous for Hb Ottawa (HBA2:c.46G>C) and β+ thalassemia (HBB:c.-138C>T). This case represents the first reported finding of Hb Ottawa in the Indian population, as well as the first time capillary zone electrophoresis (CZE) has been used to identify the variant. The abnormal red cell indices were attributed to co-inheritance of β+ thalassemia mutation (HBB:c.-138C>T), which alters binding of transcriptional factors to the HBB promoter and reduces transcription from the allele. The mild β+ thalassemia mutation has commonly been found in the Indian population.

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