|
Status |
Public on Nov 18, 2024 |
Title |
C-M34-7 |
Sample type |
SRA |
|
|
Source name |
Th-MYCN Tumor
|
Organism |
Mus musculus |
Characteristics |
tissue: Th-MYCN Tumor treatment: Control infiltration: F
|
Treatment protocol |
Recruited Th-MYCN animals were treated with saline control or TEPA (400mg/kg) for three or seven days before tumor collection.
|
Growth protocol |
Th-MYCN transgenic animals were recruited for treatment when a small tumor (3-4mm diameter) was manually palpated.
|
Extracted molecule |
total RNA |
Extraction protocol |
A tissue microarray (TMA) was prepared using 20 Th-MYCN tumor samples (10 control, 10 TEPA-treated) in duplicate, cored at 1mm. Coring sites were chosen at random with areas exhibiting necrosis were excluded prior by an experienced histopathologist using a hematoxylin-eosin stain. The FFPE TMA block was sectioned at 4µm and transferred to a Bond Plus slide (Leica Biosystems). In brief, slides were hybridized with the GeoMx Mouse Whole Transcriptome Atlas followed by immunofluorescent staining with pan-cytokeratin (Thermo Fisher Scientific; #53-9003-82) for identification of tumor cells, smooth muscle actin (Abcam; #ab184675) for extracellular matrix, CD45 (Cell Signaling Technology; #35154) for all hematopoietic cells and DNA GeoMx Nuclear Stain (NanoString; #121303303) for cell nuclei. The sectioned FFPE TMA block was processed by the NanoString GeoMx DSP Technology Access Program according to manufacturer's instructions.
|
|
|
Library strategy |
OTHER |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
TMA slides were hybridized with the GeoMx Mouse Whole Transcriptome Atlas (~18,000 targets) to generate FASTQ files. Assembly: mm10 Supplementary files format and content: *.dcc = digital count conversion files Supplementary files format and content: Mm_R_NGS_WTA_v1.0.pkc = NanoString Probe Kit Configuration file Library strategy: Spatial Transcriptomics
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|
|
Submission date |
Nov 13, 2024 |
Last update date |
Nov 18, 2024 |
Contact name |
Orazio Vittorio |
E-mail(s) |
[email protected]
|
Organization name |
UNSW Sydney
|
Department |
School of Biomedical Sciences, Faculty of Medicine
|
Lab |
Metal-Targeted Therapy & Immunology (MTTI)
|
Street address |
High St
|
City |
Kensington |
ZIP/Postal code |
2033 |
Country |
Australia |
|
|
Platform ID |
GPL13112 |
Series (1) |
GSE281844 |
Copper chelation redirects neutrophil function to enhance anti-GD2 antibody therapy in neuroblastoma [GeoMx] |
|
Relations |
BioSample |
SAMN44665618 |
SRA |
SRX26678008 |