Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia

CBAVD is congenital defect, data concerning the report of CBAVD case have not been reporting in Indonesia. The aim of this research to determine potency mutan ΔF 508-T gene CFTR could be used as prototype for therapy congenital defect CBAVD in Indonesia. Blood sample from Azoospermi man was collec...

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Main Author: Maslichah Mafruchati
Format: Theses and Dissertations NonPeerReviewed
Language:Indonesian
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Published: 2015
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Online Access:http://repository.unair.ac.id/63550/1/1.%20HALAMAN%20JUDUL.pdf
http://repository.unair.ac.id/63550/2/2.%20ABSTRAK.pdf
http://repository.unair.ac.id/63550/3/3.%20BAB%201.pdf
http://repository.unair.ac.id/63550/4/4.%20BAB%202.pdf
http://repository.unair.ac.id/63550/5/5.%20BAB%203.pdf
http://repository.unair.ac.id/63550/6/6.%20BAB%204.pdf
http://repository.unair.ac.id/63550/7/7.%20BAB%205.pdf
http://repository.unair.ac.id/63550/8/8.%20BAB%206.pdf
http://repository.unair.ac.id/63550/9/9.%20BAB%207.pdf
http://repository.unair.ac.id/63550/10/10.%20DAFTAR%20PUSTAKA.pdf
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spelling id-langga.635502020-05-26T05:18:25Z http://repository.unair.ac.id/63550/ Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia Maslichah Mafruchati R735-854 Medical education. Medical schools. Research CBAVD is congenital defect, data concerning the report of CBAVD case have not been reporting in Indonesia. The aim of this research to determine potency mutan ΔF 508-T gene CFTR could be used as prototype for therapy congenital defect CBAVD in Indonesia. Blood sample from Azoospermi man was collected and measured by R Neacy-QIAGENKit to compare their quality. Three different primers were used in this research. The result of SDS-PAGE method was positive to find molecular weight CFTR protein in CBAVD patient. The result of research showed that man with CBAVD have level base pair on 400bp in CBAVD patient in Indonesia, detection of Adenovirus was negative by PCR, this support that was truly congenital disease, The result of SDS_PAGE to measure molecular weight CFTR protein were 190-250kDA, 170-180k Da, 140-160kDA and 120kDa and the score of Immunoglobuline G was 15579 mg/dl measured by Cobas C6000 Immunoturbidimetri. The level base pair on 400 bp of DNA mutant ΔF 508-T gene Code CFTR will guide strategies for developing new therapeutics and alternative theraphy toward defect congenital CBAVD in Indonesia 2015 Thesis NonPeerReviewed text id http://repository.unair.ac.id/63550/1/1.%20HALAMAN%20JUDUL.pdf text id http://repository.unair.ac.id/63550/2/2.%20ABSTRAK.pdf text id http://repository.unair.ac.id/63550/3/3.%20BAB%201.pdf text id http://repository.unair.ac.id/63550/4/4.%20BAB%202.pdf text id http://repository.unair.ac.id/63550/5/5.%20BAB%203.pdf text id http://repository.unair.ac.id/63550/6/6.%20BAB%204.pdf text id http://repository.unair.ac.id/63550/7/7.%20BAB%205.pdf text id http://repository.unair.ac.id/63550/8/8.%20BAB%206.pdf text id http://repository.unair.ac.id/63550/9/9.%20BAB%207.pdf text id http://repository.unair.ac.id/63550/10/10.%20DAFTAR%20PUSTAKA.pdf Maslichah Mafruchati (2015) Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia. Disertasi thesis, Universitas Airlangga. http://lib.unair.ac.id
institution Universitas Airlangga
building Universitas Airlangga Library
country Indonesia
collection UNAIR Repository
language Indonesian
Indonesian
Indonesian
Indonesian
Indonesian
Indonesian
Indonesian
Indonesian
Indonesian
Indonesian
topic R735-854 Medical education. Medical schools. Research
spellingShingle R735-854 Medical education. Medical schools. Research
Maslichah Mafruchati
Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia
description CBAVD is congenital defect, data concerning the report of CBAVD case have not been reporting in Indonesia. The aim of this research to determine potency mutan ΔF 508-T gene CFTR could be used as prototype for therapy congenital defect CBAVD in Indonesia. Blood sample from Azoospermi man was collected and measured by R Neacy-QIAGENKit to compare their quality. Three different primers were used in this research. The result of SDS-PAGE method was positive to find molecular weight CFTR protein in CBAVD patient. The result of research showed that man with CBAVD have level base pair on 400bp in CBAVD patient in Indonesia, detection of Adenovirus was negative by PCR, this support that was truly congenital disease, The result of SDS_PAGE to measure molecular weight CFTR protein were 190-250kDA, 170-180k Da, 140-160kDA and 120kDa and the score of Immunoglobuline G was 15579 mg/dl measured by Cobas C6000 Immunoturbidimetri. The level base pair on 400 bp of DNA mutant ΔF 508-T gene Code CFTR will guide strategies for developing new therapeutics and alternative theraphy toward defect congenital CBAVD in Indonesia
format Theses and Dissertations
NonPeerReviewed
author Maslichah Mafruchati
author_facet Maslichah Mafruchati
author_sort Maslichah Mafruchati
title Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia
title_short Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia
title_full Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia
title_fullStr Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia
title_full_unstemmed Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia
title_sort potensi mutan δf 508-t gen pengkode cystic fibrosis transmembrane conductance regulator (cftr) sebagai prototype pada penyakit congenital bilateral absence of vas deferens (cbavd) di indonesia
publishDate 2015
url http://repository.unair.ac.id/63550/1/1.%20HALAMAN%20JUDUL.pdf
http://repository.unair.ac.id/63550/2/2.%20ABSTRAK.pdf
http://repository.unair.ac.id/63550/3/3.%20BAB%201.pdf
http://repository.unair.ac.id/63550/4/4.%20BAB%202.pdf
http://repository.unair.ac.id/63550/5/5.%20BAB%203.pdf
http://repository.unair.ac.id/63550/6/6.%20BAB%204.pdf
http://repository.unair.ac.id/63550/7/7.%20BAB%205.pdf
http://repository.unair.ac.id/63550/8/8.%20BAB%206.pdf
http://repository.unair.ac.id/63550/9/9.%20BAB%207.pdf
http://repository.unair.ac.id/63550/10/10.%20DAFTAR%20PUSTAKA.pdf
http://repository.unair.ac.id/63550/
http://lib.unair.ac.id
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