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dc.contributor.authorAmini, N
dc.contributor.authorBayat, A-A
dc.contributor.authorZarei, O
dc.contributor.authorHadavi, R
dc.contributor.authorMahmoudian, J
dc.contributor.authorMahmoudi, AR
dc.contributor.authorDarzi, M
dc.contributor.authorRabbani, H
dc.contributor.authorJeddi-Tehrani, M
dc.date.accessioned2018-08-26T08:32:34Z
dc.date.available2018-08-26T08:32:34Z
dc.date.issued2015
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52307
dc.description.abstractActin is one of the most widely studied structural and multifunctional housekeeping proteins in eukaryotic cells with important roles in many cell functions. Antibodies against ?-actin and other housekeeping gene-encoded proteins are used as internal loading controls in Western blot analyses. The aim of this study was to produce a monoclonal antibody (mAb) against a synthetic peptide derived from N-terminal region of ?-actin and to study its reactivity with different organisms. A synthetic peptide, derived from ?-actin, was designed and used to produce a mAb by hybridoma technology. The produced antibody (clone 4E5- A10) was purified by an affinity chromatography column followed by characterization of purified mAb using SDS-PAGE, ELISA and Western blot. Our results showed that 4E5-A10 was an IgM and had desired purity and excellent reactivity with the immunizing peptide with an affinity constant of 2.7أ—108 M-1. It could detect a band of about 45 kDa, corresponding to ?-actin, in Western blot. Furthermore, it could react in a more sensitive manner and with a wider range of organisms than a known commercial anti ?-actin antibody. Our data suggest that 4E5-A10 can act as a sensitive probe for detection of ?-actin as an internal loading control, for a wide range of organisms, in Western blot analyses. é 2015 Bentham Science Publishers.
dc.language.isoEnglish
dc.relation.ispartofProtein and Peptide Letters
dc.subjectbeta actin
dc.subjectmonoclonal antibody
dc.subjectmonoclonal antibody 4E5 A10
dc.subjectunclassified drug
dc.subjectactin
dc.subjectimmunoglobulin M
dc.subjectmonoclonal antibody
dc.subjectpeptide
dc.subjectamino terminal sequence
dc.subjectanimal cell
dc.subjectantibody detection
dc.subjectantibody titer
dc.subjectantigen binding
dc.subjectaphid
dc.subjectArticle
dc.subjectbinding affinity
dc.subjectconjugation
dc.subjectcontrolled study
dc.subjectcoral
dc.subjectDaphnia magna
dc.subjectDrosophila melanogaster
dc.subjectEriocheir sinensis
dc.subjectfemale
dc.subjectfish
dc.subjectgoldfish
dc.subjectimmunoreactivity
dc.subjectLitopenaeus vannamei
dc.subjectMacrosiphum rosae
dc.subjectmouse
dc.subjectnonhuman
dc.subjectParacheirodon innesi
dc.subjectprotein interaction
dc.subjectSeriatopora hystrix
dc.subjectWestern blotting
dc.subjectaffinity chromatography
dc.subjectamino acid sequence
dc.subjectanimal
dc.subjectantibody affinity
dc.subjectBagg albino mouse
dc.subjectchemistry
dc.subjectenzyme linked immunosorbent assay
dc.subjectimmunology
dc.subjectisolation and purification
dc.subjectpolyacrylamide gel electrophoresis
dc.subjectEukaryota
dc.subjectActins
dc.subjectAmino Acid Sequence
dc.subjectAnimals
dc.subjectAntibodies, Monoclonal
dc.subjectAntibody Affinity
dc.subjectBlotting, Western
dc.subjectChromatography, Affinity
dc.subjectElectrophoresis, Polyacrylamide Gel
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subjectFemale
dc.subjectImmunoglobulin M
dc.subjectMice, Inbred BALB C
dc.subjectPeptides
dc.titleA novel monoclonal antibody against a synthetic peptide from ?-actin can react with its corresponding protein
dc.typeArticle
dc.citation.volume22
dc.citation.issue5
dc.citation.spage419
dc.citation.epage424
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.2174/0929866522666141231111618


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