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
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/37574
Ver los metadatos del registro completo
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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 |
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reponame:SEDICI (UNLP) instname:Universidad Nacional de La Plata instacron:UNLP |
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SEDICI (UNLP) |
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Universidad Nacional de La Plata |
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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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12.749369 |