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Status |
Public on Nov 29, 2019 |
Title |
SH-SY5Y cells, Nrp1-IP-2 |
Sample type |
SRA |
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Source name |
SH-SY5Y cells
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Organism |
Homo sapiens |
Characteristics |
cell line: SH-SY5Y cell type: neuroblastoma cells rip antibody: rabbit-anti-Nrp1 (Abcam, ab81321)
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Growth protocol |
The cells were cultured at 37C and 5% CO2 in DMEM high glucose medium supplemented with 10% FBS
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Extracted molecule |
total RNA |
Extraction protocol |
The lysate of SH-SY5Y cells was incubated with magnetic Dynabeads pre-coupled with antibodies (mouse-anti-DCC (BD Biosciences, 554223); rabbit-anti-Nrp1 (Abcam, ab81321)) for 1.5 hours at 4°C. Beads were then washed 3 times and processed for RNA isolation. Immunopurified RNAs are reverse-transcribed, and then amplified by a PCR-based method (Tang et al., Nat Methods 6, 2009).
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Library strategy |
RIP-Seq |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
Illumina NextSeq 500 |
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Data processing |
Illumina bcl2fastq2 Conversion Software v2.20 was used for de-multiplexing and base-calling. Sequence reads were aligned to the genome using Hisat2 v2.1.0 Read counts for each gene were determined using HTSeq version 0.11.0. Genome_build: hg19 Supplementary_files_format_and_content: tab-delimited text files include read counts for each gene
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Submission date |
Aug 03, 2019 |
Last update date |
Nov 30, 2019 |
Contact name |
Christine E Holt |
Organization name |
University of Cambridge
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Department |
Department of PDN
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Street address |
Anatomy Bldg., Downing St.
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City |
Cambridge |
ZIP/Postal code |
CB2 3DY |
Country |
United Kingdom |
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Platform ID |
GPL18573 |
Series (1) |
GSE135338 |
Receptor-specific interactome as a hub for rapid cue-induced selective translation in axons |
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Relations |
BioSample |
SAMN12478801 |
Supplementary file |
Size |
Download |
File type/resource |
GSM4006653_Nrp1-IP-2_count.txt.gz |
137.2 Kb |
(ftp)(http) |
TXT |
Raw data are available in SRA |
Processed data provided as supplementary file |
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