The study for personal identification using DNA profiling method by organized bone marrows.
The study for personal identification using DNA profiling method by organized bone marrows.
批准号:
07670495
负责人:
KUBO Shin-ichi
金额:
$1.41万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996
中文摘要
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英文摘要
We examined the organized human bone marrows with the aim of personal identification using PCR (the Polymerase Chain Reaction) analysis, that is sex determination and STR (short tandem repeats). The purpose of the present research is to disclose the optimum device to detection of DNA polymorphism with degraded DNA samples. The subjects were 38 manubrium sterni sampled at autopsies. We left them outdoor for periods from two weeks to 36 months, then DNA samples were extracted from bone marrows.1.We compared two primers of different bp length from amelogenin gene for sex determination. The sex identifications in 18 subjects were determinable with longer bp AMGL at first PCR analysis. Regarding to the other sex undeterminable cases, even then ten cases have still **en undeterminable although we took low molecules away and added BSA at PCR and moreover we tested Dual PCR.On the contrary, 25 ***aples were sex determinable with shorter bp AMGL at first PCR analysis. All cases have been sex de … More terminable when we performed PCRs when we removed low molecules form samples and added BSA.Thus we have arrived at the conclusion that followings are necessary to determine sexes with degraded DNA samples. Those are removal of low molecules and addition of BSA to the DNA samples Then designing shorter bp primer is preferable.2.We investigated STR types with vWF and TH01. Then we assessed the results whether or not those results would coincide between the samples providing from organized bone marrows and the blood DNA samples from each of the same individuals at autopsies. Thirteen samples were not amplified without preparation of DNA just the same as sex determination, but the products of all cases were clearly visible following the above preparation. The bands from organized bone marrow DNA and blood DNA at the time of autopsy coincided in all cases. Since both vWF and TH01 are shorter primers, when personal identification is demonstrated from organized DNA,it is necessary to increase the sensitivity of detection regarding to both DNA preparation and designing of the primers. Less
期刊论文(4)
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会议论文
折原 義行: "陳旧骨髄からのAMXプライア-を用いたPCR法による性別判定" DNA多型. 3. 280-284 (1995)
Yoshiyuki Orihara:“利用 AMX 先验从旧骨髓中通过 PCR 方法确定性别”DNA 多态性。 3. 280-284 (1995)
DOI:
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作者:
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通讯作者:
折原義行: "陳旧骨髄からのAMXYプライマーを用いたPCR法による性別判定" DNA多型. 3. 280-284 (1995)
Yoshiyuki Orihara:“使用来自旧骨髓的 AMXY 引物通过 PCR 方法确定性别”DNA 多态性。 3. 280-284 (1995)
DOI:
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发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Orihara, Yoshiyuki: "Sex identification by PCR using AMXY Primer from Organized Bone Marrow" DNA Polymorphism. 3. 280-284 (1995)
Orihara, Yoshiyuki:“使用组织骨髓中的 AMXY 引物通过 PCR 进行性别鉴定”DNA 多态性。
DOI:
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发表时间:
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作者:
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通讯作者:
Application of mRNA expression analysis for human blood identification to degenerated samples that were false-negative by immunochromatography
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