摘要
We describe the precise identification, separation and quantitation of several haemoglobin (Hb) variants such as Hbs A2, A, F, S, E, J, H, D-Punjab and Q-India in untransfused patients with beta thalassaemia and other haemoglobinopathies prevalent in the Indian population using whole blood (5 microliters), red cell lysates (2 microliters) or dried blood specimens on filter paper, using a conventional anion exchange high performance liquid chromatography (AX-HPLC) system. Samples were simultaneously studied for the presence of haemoglobin variants by alkaline electrophoresis. The problems in analysing rare variants and separating the closely migrating variants, encountered in the conventional methods could be resolved using the HPLC technique.
Subject(s)
Adult , Case-Control Studies , Child , Chromatography, High Pressure Liquid/methods , Chromatography, Ion Exchange/methods , Female , Genetic Variation , Hemoglobinopathies/diagnosis , Hemoglobins/genetics , Humans , Male , beta-Thalassemia/diagnosis摘要
Sera of 37 patients attending the allergic clinic and of 10 normal healthy non-allergic controls were collected and in a double blind manner they were tested using phadiatop RIA for differentiation of patient's symptoms as due to atopy or otherwise without performing other troublesome investigations. It is an easy, less time consuming and reliable technique.