dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorMuseu Paraense Emilio Goeldi
dc.contributorUniversidade Federal do Pará (UFPA)
dc.date.accessioned2014-05-27T11:22:35Z
dc.date.accessioned2022-10-05T18:08:28Z
dc.date.available2014-05-27T11:22:35Z
dc.date.available2022-10-05T18:08:28Z
dc.date.created2014-05-27T11:22:35Z
dc.date.issued2007-09-03
dc.identifierGenetics and Molecular Research, v. 6, n. 2, p. 415-421, 2007.
dc.identifier1676-5680
dc.identifierhttp://hdl.handle.net/11449/69876
dc.identifierWOS:000251696400019
dc.identifier2-s2.0-34548282227
dc.identifier2-s2.0-34548282227.pdf
dc.identifier3279428066176719
dc.identifier0000-0002-4603-9467
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3919252
dc.description.abstractStudies of the hemoglobin pattern in Brazilian reptiles are important for determining ecological and phylogenetic relationships, but they are scarce. Peripheral blood samples were obtained from 7 males and 18 females of Rhinoclemmys punctularia. The hematological profile was based on the total hemoglobin and hematocrit values. The hemoglobin profile was obtained using electrophoretic procedures at different pH, isoelectric focusing, globin chain electrophoresis, and HPLC. The hematocrit (31 ± 2%) and total hemoglobin (7.5 ± 0.2 g/dL) values did not indicate gender variations. Alkaline pH electrophoresis of the total blood samples treated with 1% saponin demonstrated the presence of four well-defined hemoglobin fractions, one major component (fraction I), showing cathodic migration and three others faster than fraction I with anodic migration. When the samples were precipitated with chloroform, only two hemoglobin fractions were observed, similar to fractions I and III from the first procedure. Isoelectric focusing and HPLC showed the same pattern. With acid and neutral pH electrophoresis, two fractions with anodic migration were observed. The globin chain identification at alkaline pH showed two fractions, but four fractions were observed at acidic pH, suggesting that different polypeptide chains are involved in the hemoglobin molecule. The chromatographic separation of the total blood sample demonstrated that the major fraction comprised 81.9% and the minor 18.1%. The results obtained demonstrated a similarity between these hemoglobin components and those of some Chelidae reported in the literature for both land and aquatic animals, reflecting the adaptation to environmental conditions. ©FUNPEC-RP.
dc.languageeng
dc.relationGenetics and Molecular Research
dc.relation0,439
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectElectrophoretic profile
dc.subjectHemoglobin polymorphism
dc.subjectHemoglobins
dc.subjectRhinoclemmys punctularia
dc.subjectchloroform
dc.subjecthemoglobin
dc.subjectalkalinity
dc.subjectcontrolled study
dc.subjectelectrophoresis
dc.subjectfemale
dc.subjecthematocrit
dc.subjecthemoglobin determination
dc.subjecthigh performance liquid chromatography
dc.subjectisoelectric focusing
dc.subjectmale
dc.subjectnonhuman
dc.subjectpH
dc.subjectpH measurement
dc.subjectsex difference
dc.subjectturtle
dc.subjectAnimals
dc.subjectChromatography
dc.subjectEcology
dc.subjectElectrophoresis
dc.subjectFemale
dc.subjectHematocrit
dc.subjectHumans
dc.subjectMale
dc.subjectModels, Genetic
dc.subjectPhylogeny
dc.subjectPolymorphism, Genetic
dc.subjectReptiles
dc.subjectTurtles
dc.subjectAnimalia
dc.subjectChelidae
dc.subjectReptilia
dc.titleDescription of electrophoretic and chromatographic hemoglobin profile of Rhinoclemmys punctularia
dc.typeArtigo


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