- 【Updated on May 12, 2025】 Integration of CiNii Dissertations and CiNii Books into CiNii Research
- Trial version of CiNii Research Knowledge Graph Search feature is available on CiNii Labs
- Suspension and deletion of data provided by Nikkei BP
- Regarding the recording of “Research Data” and “Evidence Data”
Identification of HLA‐C alleles using PCR—single‐strand‐conformation polymorphism and direct sequencing
Search this article
Description
<jats:p>Alleles encoding HLA‐C antigens in Japanese were identified by polymerase chain reaction followed by single strand conformation polymorphism (PCR‐SSCP) and nucleotide sequencing analyses. The results showed that at least sixteen different alleles code for eight serologically detectable antigen groups and undetectable blanks. Cwl was mainly encoded by Cw*0102, whereas two split antigens of Cw3, Cw9 and Cw10, were encoded by Cw*0303 and Cw*0304, respectively. Cw4 and Cw6 were encoded by Cw*0401 and Cw*0602, respectively. Seven alleles, Cw*0801, Cw*0803, Cw*1202, Cw*1203, Cw*1402, Cw*1403 and Cw*1502, were found to encode serological HLA‐C “blanks” in Japanese. Moreover, errors in the published nucleotide sequences of Cw*0501 and Cw*1201 were corrected. Twenty‐one HLA‐C alleles were distinguished from each other by means of group‐specific PCR amplification followed by the SSCP method developed in the present study. The system using genomic DNAs can be used effectively for identification of new HLA‐C alleles.</jats:p>
Journal
-
- Tissue Antigens
-
Tissue Antigens 49 (2), 134-140, 1997-02
Wiley