Literature DB >> 17951209

Hemoglobin Ypsilanti: a high-oxygen-affinity hemoglobin demonstrated by two automated high-pressure liquid chromatography systems.

Daniel D Mais1, Laurence A Boxer, Ronald D Gulbranson, David F Keren.   

Abstract

Hemoglobin (Hb) Ypsilanti is a rare high-oxygen-affinity hemoglobin. Like other high-oxygen-affinity hemoglobins, Hb Ypsilanti manifests as erythrocytosis. Because the migration of many high-oxygen-affinity variants on alkaline and acid gels does not differ from that of HbA, oxygen-hemoglobin dissociation studies are often used to document their presence. Hb Ypsilanti is a notable exception because its electrophoresis pattern on alkaline gel is highly characteristic, exemplifying the phenomenon of hybrid formation in variant hemoglobins. In the past few years, several laboratories have begun to use high-pressure liquid chromatography (HPLC) as a screen for hemoglobinopathies. We demonstrate the elution profile of Hb Ypsilanti on the 2 most widely used HPLC methods.

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Year:  2007        PMID: 17951209     DOI: 10.1309/WAE8JNK656CQAQL5

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  1 in total

1.  Haemoglobinopathia Ypsilanti - A rare, but important differential diagnosis to polycythaemia vera.

Authors:  Marietta Nygaard; Jesper Petersen; Ole W Bjerrum
Journal:  Leuk Res Rep       Date:  2013-10-09
  1 in total

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