HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP

Autores
Abba, Martín Carlos; Gómez, María Atilia; Golijow, Carlos Daniel
Año de publicación
2001
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
In the present study we used a simple and reliable method for HLA-DQA1 allele typing based on the single-stranded conformation polymorphism (SSCP) properties of DNA molecules obtained by PCR. The technique consists of PCR amplification of a DNA fragment comprising the second exon of the HLA-DQA1 gene, amplicon denaturation using a low ionic strength solution (LIS), and electrophoresis on a small native polyacrylamide gel, followed by a rapid silver staining procedure. In order to validate the technique and to obtain the allele patterns for the DQA1 gene, 50 cervical samples were typed using this methodology and the commercial Amplitype® HLA DQA1 Amplification and Typing kit. All the alleles detected with the kit were characterized by the LIS-SSCP approach. This procedure proved to be useful for population screening and typing of the DQA1 gene as well as for detecting new alleles or mutations in the donor-recipient molecular matching of HLA class II genes.
Facultad de Ciencias Veterinarias
Materia
Ciencias Veterinarias
agar gel electrophoresis
HLA-DQA1
LIS-SSCP
genetics
PCR
osmolarity
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc/3.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/37574

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repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCPAbba, Martín CarlosGómez, María AtiliaGolijow, Carlos DanielCiencias Veterinariasagar gel electrophoresisHLA-DQA1LIS-SSCPgeneticsPCRosmolarityIn the present study we used a simple and reliable method for HLA-DQA1 allele typing based on the single-stranded conformation polymorphism (SSCP) properties of DNA molecules obtained by PCR. The technique consists of PCR amplification of a DNA fragment comprising the second exon of the HLA-DQA1 gene, amplicon denaturation using a low ionic strength solution (LIS), and electrophoresis on a small native polyacrylamide gel, followed by a rapid silver staining procedure. In order to validate the technique and to obtain the allele patterns for the DQA1 gene, 50 cervical samples were typed using this methodology and the commercial Amplitype® HLA DQA1 Amplification and Typing kit. All the alleles detected with the kit were characterized by the LIS-SSCP approach. This procedure proved to be useful for population screening and typing of the DQA1 gene as well as for detecting new alleles or mutations in the donor-recipient molecular matching of HLA class II genes.Facultad de Ciencias Veterinarias2001-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf867-869http://sedici.unlp.edu.ar/handle/10915/37574enginfo:eu-repo/semantics/altIdentifier/url/http://www.scielo.br/pdf/bjmbr/v34n7/4121.pdfinfo:eu-repo/semantics/altIdentifier/issn/0100-879Xinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc/3.0/Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T10:49:36Zoai:sedici.unlp.edu.ar:10915/37574Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 10:49:37.313SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP
title HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP
spellingShingle HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP
Abba, Martín Carlos
Ciencias Veterinarias
agar gel electrophoresis
HLA-DQA1
LIS-SSCP
genetics
PCR
osmolarity
title_short HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP
title_full HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP
title_fullStr HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP
title_full_unstemmed HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP
title_sort HLA-DQA1 allele typing by nonisotopic PCR-LIS-SSCP
dc.creator.none.fl_str_mv Abba, Martín Carlos
Gómez, María Atilia
Golijow, Carlos Daniel
author Abba, Martín Carlos
author_facet Abba, Martín Carlos
Gómez, María Atilia
Golijow, Carlos Daniel
author_role author
author2 Gómez, María Atilia
Golijow, Carlos Daniel
author2_role author
author
dc.subject.none.fl_str_mv Ciencias Veterinarias
agar gel electrophoresis
HLA-DQA1
LIS-SSCP
genetics
PCR
osmolarity
topic Ciencias Veterinarias
agar gel electrophoresis
HLA-DQA1
LIS-SSCP
genetics
PCR
osmolarity
dc.description.none.fl_txt_mv In the present study we used a simple and reliable method for HLA-DQA1 allele typing based on the single-stranded conformation polymorphism (SSCP) properties of DNA molecules obtained by PCR. The technique consists of PCR amplification of a DNA fragment comprising the second exon of the HLA-DQA1 gene, amplicon denaturation using a low ionic strength solution (LIS), and electrophoresis on a small native polyacrylamide gel, followed by a rapid silver staining procedure. In order to validate the technique and to obtain the allele patterns for the DQA1 gene, 50 cervical samples were typed using this methodology and the commercial Amplitype® HLA DQA1 Amplification and Typing kit. All the alleles detected with the kit were characterized by the LIS-SSCP approach. This procedure proved to be useful for population screening and typing of the DQA1 gene as well as for detecting new alleles or mutations in the donor-recipient molecular matching of HLA class II genes.
Facultad de Ciencias Veterinarias
description In the present study we used a simple and reliable method for HLA-DQA1 allele typing based on the single-stranded conformation polymorphism (SSCP) properties of DNA molecules obtained by PCR. The technique consists of PCR amplification of a DNA fragment comprising the second exon of the HLA-DQA1 gene, amplicon denaturation using a low ionic strength solution (LIS), and electrophoresis on a small native polyacrylamide gel, followed by a rapid silver staining procedure. In order to validate the technique and to obtain the allele patterns for the DQA1 gene, 50 cervical samples were typed using this methodology and the commercial Amplitype® HLA DQA1 Amplification and Typing kit. All the alleles detected with the kit were characterized by the LIS-SSCP approach. This procedure proved to be useful for population screening and typing of the DQA1 gene as well as for detecting new alleles or mutations in the donor-recipient molecular matching of HLA class II genes.
publishDate 2001
dc.date.none.fl_str_mv 2001-07
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/37574
url http://sedici.unlp.edu.ar/handle/10915/37574
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.scielo.br/pdf/bjmbr/v34n7/4121.pdf
info:eu-repo/semantics/altIdentifier/issn/0100-879X
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc/3.0/
Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc/3.0/
Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)
dc.format.none.fl_str_mv application/pdf
867-869
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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