5-Maleimido-eosin
5-Maleimido-eosin structure
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Common Name | 5-Maleimido-eosin | ||
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| CAS Number | 150322-02-4 | Molecular Weight | 742.94700 | |
| Density | 2.5g/cm3 | Boiling Point | 773.9ºC at 760 mmHg | |
| Molecular Formula | C24H9Br4NO7 | Melting Point | N/A | |
| MSDS | Chinese | Flash Point | 421.9ºC | |
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Rotational motions of myosin heads in myofibril studied by phosphorescence anisotropy decay measurements.
J. Biol. Chem. 262 , 8314, (1987) We studied the rotational Brownian motions of myosin heads, of which the sulfhydryl group was selectively labeled with the triplet probe 5-eosinylmaleimide, in myofibril by using flash-induced phosphorescence anisotropy decay measurements. The anisotropy deca... |
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Rotational diffusion of eosin-labeled pyruvate dehydrogenase complex of Escherichia coli.
Eur. J. Biochem. 121 , 233, (1981) The enzymatically reduced lipoyl residues of the transacetylase component of the pyruvate dehydrogenase complex from Escherichia coli were labeled with eosin maleimide. Using eosin as triplet probe, triplet-triplet absorption dichroism measurements were perfo... |
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Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.
Haematologica 97 , 516-523, (2012) The laboratory diagnosis of hereditary spherocytosis commonly relies on NaCl-based or glycerol-based red cell osmotic fragility tests; more recently, an assay directly targeting the hereditary spherocytosis molecular defect (eosin-5'-maleimide-binding test) h... |
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Use of capillary blood to diagnose hereditary spherocytosis.
Pediatr. Blood Cancer 59 , 1299-1301, (2012) We studied 31 children with hemolytic anemia, or with positive family history for hereditary spherocytosis (HS), to assess the reliability of capillary blood samples for the diagnosis. HS was diagnosed in 20 patients. Cryohemolysis (CH) was positive in 94% an... |
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dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state.
Eur. J. Haematol. 88 , 350-355, (2012) Mutations in the anion exchanger 1 (AE1) gene encoding the erythroid and kidney anion (chloride-bicarbonate) exchanger 1 may result in familial distal renal tubular acidosis (dRTA) in association with membrane defect hemolytic anemia. Seven children presentin... |
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Delay in the measurement of eosin-5'-maleimide (EMA) binding does not affect the test result for the diagnosis of hereditary spherocytosis. Ciepiela O, Kotuła I, Górska E, et al.
Clin. Chem. Lab Med. 0 , 1-7, (2012)
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