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Mengurai Hadis Tahnik dan Gerakan Anti Vaksin Anif Yuni Muallifah
Jurnal Living Hadis Vol 2, No 2 (2017)
Publisher : Universitas Islam Negeri Sunan Kalijaga Yogyakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (540.91 KB) | DOI: 10.14421/livinghadis.2017.1334

Abstract

Yogyakarta pada bulan Juli 2017 gempar dengan berita adanya beberapa sekolah berbasis agama yang menolak vaksinasi pada program imunisasi MR (Measles Rubbela) yang menjadi program pemerintah. Gerakan anti vaksin memang telah lama ada baik di Indonesia maupun di luar negeri. Beberapa dari mereka menggunakan argumen teologis unntuk menolak vaksinasi. Hadits tahnik di gunakan sebagai salah satu alasan utama bahwa Islam sudah mengajarkan metode imunisasi paling unggul karena berdasarkan petunjuk nabi yang berasal dari wahyu Tuhan, sehingga program imunisasi yang dilakukan pemerintah di anggap sudah tidak diperlukan lagi. Paper ini meguraikan bagaimana sebenarnya pemahaman hadits tahnik ini dari sisi ilmu hadits, ilmu biologi, otentisitasnya, dan relevansinya dalam polemik anti vaksin di Indonesia.
ISOLASI DAN ANALISIS KUALITAS DNA PLASMID (pGEM®-3Zf(+)) SEBAGAI SEDIAAN KEBUTUHAN PRAKTIKUM DI LAB. BIOLOGI FST Arifah Khusnuryani; Jumailatus Solihah; Anif Yuni Muallifah
Integrated Lab Journal Vol. 4 No. 1 (2016)
Publisher : UIN Sunan Kalijaga Yogyakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (293.89 KB) | DOI: 10.14421/ilj.2016.%x

Abstract

Implementation of practical work in biology laboratory needs supporting media including laboratory equipments and materials. In genetics and molecular biology, the routine materials are mostly molecular resources, which are produced by certain company. To get the materials, we must order and pay for a relative high price.These molecular resources in biology laboratory is not only beneficial for practical activity, but also useful for research activity in related fields.This research works as an application of methods applied in laboratory to result in a product that is valuable in practical works, i.e. the pGEM plasmids. The methods that were employed involved the transformation of E. coli with pGEM plasmid, blue-white screening by using X-gal, and plasmid isolation by alkaline lysis method. The transformation results showed a relative low efficiency at 1,2 x 103cfu/µg DNA. The electrophoresis in 0.8% agarose gel demonstrated that the plasmid DNA was successfully isolated with some thin bands at position 3000-4000bp, despite of a large chromosomal DNA and some smear RNA were still observed. The DNA obtained is pure enough, characterized by the ratio of A260/280 at the range of 1,8-2,0.