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Sample GSM4405446 Query DataSets for GSM4405446
Status Public on Oct 06, 2023
Title CD138+cells from normal_Replicate 1
Sample type RNA
 
Source name Bone marrow CD138+ cells,normal,replicate 1
Organism Homo sapiens
Characteristics disease state: Normal
tissue: bone marrow
cell type: CD138+ cells
gender: Female
age: 59
Extracted molecule total RNA
Extraction protocol Bone marrow CD138+ cells were obtained from multiple myeloma patients and normal individuals by magnetic bead separation. The cells were treated with TRIzol to extract total RNA according to manufactures' instrctions.
Label Cy3
Label protocol mRNA was purified from total RNA after removal of rRNA (mRNA-ONLY™ Eukaryotic mRNA Isolation Kit, Epicentre). Then, each sample was amplified and transcribed into fluorescent cRNA along the entire length of the transcripts without 3' bias utilizing a random priming method (Arraystar Flash RNA Labeling Kit, Arraystar). The labeled cRNAs were purified by RNeasy Mini Kit (Qiagen). The concentration and specific activity of the labeled cRNAs (pmol Cy3/μg cRNA) were measured by NanoDrop ND-1000
 
Hybridization protocol 1 μg of each labeled cRNA was fragmented by adding 5 μl 10 × Blocking Agent and 1 μl of 25 × Fragmentation Buffer, then heated the mixture at 60°C for 30 min, finally 25 μl 2 × GE Hybridization buffer was added to dilute the labeled cRNA. 50 μl of hybridization solution was dispensed into the gasket slide and assembled to the LncRNA expression microarray slide. The slides were incubated for 17 hours at 65°C in an Agilent Hybridization Oven.
Scan protocol The hybridized arrays were washed, fixed and scanned with using the Agilent DNA Microarray Scanner (part number G2505C).
Description lncRNA and mRMA expression data from bone marrow CD138+ cells of normal control 1
Data processing Agilent Feature Extraction software (version 11.0.1.1) was used to analyze acquired array images. Quantile normalization and subsequent data processing were performed with using the GeneSpring GX v12.1 software package (Agilent Technologies).
 
Submission date Mar 10, 2020
Last update date Oct 06, 2023
Contact name Han Yan
E-mail(s) picachu122@126.com
Organization name Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Street address Jiefang Avenue
City Wuhan
ZIP/Postal code 430022
Country China
 
Platform ID GPL21827
Series (2)
GSE146757 Microarray analysis of mRNA and long noncoding RNA expression profiles between multiple myeloma patients and control
GSE159232 Multiple myeloma patients and control

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
GE_BrightCorner 13.9192
DarkCorner 2.3621454
ASHGV40005517 2.3241003
ASHGV40014820 5.147898
ASHGV40030369 4.528701
ASHGV40013556 2.3241003
ASHGV40009737 11.863068
ASHGV40005086 10.719503
ASHGV40021163 7.6505213
ASHGV40006648 2.3241003
ASHGV40013297 6.425752
ASHGV40015652 8.597285
ASHGV40020595 4.3312902
ASHGV40006284 8.708501
ASHGV40033181 2.362197
ASHGV40006622 6.3550243
ASHGV40041510 2.3241003
ASHGV40009802 2.9058175
ASHGV40059431 2.7140632
ASHGV40053238 5.578092

Total number of rows: 61024

Table truncated, full table size 1403 Kbytes.




Supplementary file Size Download File type/resource
GSM4405446_N1.txt.gz 2.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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