| identifier |
SAMD00009630 |
| type |
biosample |
| sameAs |
|
| organism |
Mus musculus
|
| attributes |
| sample_name |
DRS002029 |
| sample comment |
Sertoli cells on 129/svj (female) x JF1 (male) backgroud were used for nuclear transfer and embryos were recovered at E13.5. The placenta was dissected from a E13.5 embryo and total RNA was prepared using RNeasy mini kit (Qiagen). Four micrograms of total RNA was used for library construction using TruSeq RNA Sample Prep Kit v2 (Illumina) according to the manufacturerâs protocol. Briefly, poly-A containing mRNAs were purified using poly-T oligo-attached magnetic beads. The purified mRNAs were fragmented using divalent cations under elevated temperatures, and then converted to dsDNA by two rounds of cDNA synthesis using reverse transcriptase and DNA polymerase I. After an end repair process, DNA fragments were ligated with adaptor oligos. The ligated products were amplified using 15 cycles of PCR to generate RNA-seq library. Library integrity was verified by Bioanalyzer DNA1000 assay (Agilent technologies). Sequencing was performed in 39bp paired end mode using Genome Analyzer IIx (Illumina). |
|
| properties ▽ |
{...}
|
| dbXrefs |
|
| distribution |
JSONJSON-LD
|
| Download |
|
| status |
public |
| visibility |
unrestricted-access |
| dateCreated |
2014-05-12T01:17:49+09:00 |
| dateModified |
2014-11-12T08:28:28+09:00 |
| datePublished |
2013-10-20T15:00:00+09:00 |