Publication:
Quantitative analysis of immunogold labeling for basic fibroblast growth factor according to the activational stages of mast cells

dc.contributor.coauthorKayton, Robert J.
dc.contributor.departmentDepartment of Mathematics
dc.contributor.departmentGraduate School of Health Sciences
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorAktaş, Ranan Gülhan
dc.contributor.kuauthorÇağlar, Mine
dc.contributor.kuauthorOktayer, Adviye Gözde
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF HEALTH SCIENCES
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:07:52Z
dc.date.issued2013
dc.description.abstractOBJECTIVE: To analyze whether immunogold labeling density for basic fibroblastic growth factor in granules is compatible with the activation stage of mast cells. STUDY DESIGN: Cytoplasmic features and granules of 46 mast cells were examined at the ultrastructural level. The cells were classified according to their activation stage, namely, whether resting, initially activated, fully degranulated or piecemeal degranulated. Granules were classified as electron lucent, moderate or dense granules. Gold particles per secretory granules in the cells were counted. Recently described quantitative analysis techniques were used for evaluation. RESULTS: There is a statistically meaningful relationship between the activation stage of mast cells and their immunogold labeling density. The number of different types of granules encountered in a cell depends on the type of the cell. The distribution of gold particles among the secretory granules depends upon the cell. The type of granule does not have an individual effect on the number of particles, as indicated by an overall statistical analysis of granules, cells and their interaction effects. CONCLUSION: A count of gold particles in the cells can be used as a strong biological indicator. Therefore the number of gold particles might be very useful for comparative studies related to the secretion of this growth factor under different conditions.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue6
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume35
dc.identifier.issn0884-6812
dc.identifier.quartileQ4
dc.identifier.scopus2-s2.0-84890613855
dc.identifier.urihttps://hdl.handle.net/20.500.14288/9219
dc.identifier.wos341746300002
dc.keywordsActivation stage
dc.keywordsBasic fibroblast growth factor
dc.keywordsBasic fibroblast growth factor receptor 1, human
dc.keywordsBFGFR protein, human
dc.keywordsImmunohistochemistry
dc.keywordsImmunogold labeling
dc.keywordsImmunogold techniques
dc.keywordsImmunolabeling techniques
dc.keywordsMast cells
dc.language.isoeng
dc.publisherSci Printers & Publ Inc
dc.relation.ispartofAnalytical and Quantitative Cytology and Histology
dc.subjectCell biology
dc.titleQuantitative analysis of immunogold labeling for basic fibroblast growth factor according to the activational stages of mast cells
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorAktaş, Ranan Gülhan
local.contributor.kuauthorÇağlar, Mine
local.contributor.kuauthorOktayer, Adviye Gözde
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit1College of Sciences
local.publication.orgunit1GRADUATE SCHOOL OF HEALTH SCIENCES
local.publication.orgunit2Department of Mathematics
local.publication.orgunit2School of Medicine
local.publication.orgunit2Graduate School of Health Sciences
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