<mods:mods version="3.3" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mods:titleInfo><mods:title>IDENTIFIKASI TIPE HLA KELAS II DENGAN TEKNIK PCR</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">Ervi</mods:namePart><mods:namePart type="family">Salwati</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>HLA (Human Leukocyte Antigen) contains a set of genes located together on the short arm &#13;
of chromosome 6. These genes control immune responses, graft acceptance or rejection and&#13;
tumor surveillance. These abilities have close relationship with genetic variation (occur in&#13;
"many forms" or alleles) that bind and present antigens to T lymphocytes.&#13;
Using advanced technology and molecular biology approaches (PCR technique) detection&#13;
of genetic variation in the HLA region (or HLA typing) has been performed based on DNA .. PCR&#13;
is an in vitro technique to amplify the DNA sequence enzymatically. "Sequence Specific Primers"&#13;
(SSP) are designed for this PCR to obtain amplification of specific alleles or groups of alleles.&#13;
The PCR products are visualized through agarose gel electrophoresis stained with ethidium&#13;
bromide.&#13;
The PCR technique requires small amount of whole blood (0.5 - I ml), gives rapid,&#13;
accurate and complete result. This paper discuss identification of HLA class &#13;
typing using&#13;
PCR-SSP technique and show the examples of the results.</mods:abstract><mods:classification authority="lcc">WC 1-100 Reference Works. General Works</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8601">2002</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>Sekretariat Badan Penelitian dan Pengembangan Kesehatan</mods:publisher></mods:originInfo><mods:genre>Article</mods:genre></mods:mods>