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Sample GSM6346284 Query DataSets for GSM6346284
Status Public on Jul 19, 2022
Title Postnatal day 14 kidney 2
Sample type RNA
 
Source name murine kidney
Organism Mus musculus
Characteristics strain: c57BJ6
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from kidneys using miRNeasy mini kits (Qiagen)
Label Cy5
Label protocol The small RNA fraction (<300 nucleotides) was hybridized on a μParaflo Microfluidic chip containing detection probes for all mouse microRNAs (miRNAs) in the miRBase version-17 (miRBase, http://microrna.sanger.ac. uk/sequences). The hybridized microarray chips were labeled with fluorescent dyes and laser scanned to obtain fluorescent images. The signal values for each sample were derived by background subtraction and normalization. Microarray chip hybridization, fluorescent labeling, laser scanning, and background subtraction and normalization were performed by LC Sciences proprietary method.
 
Hybridization protocol The small RNA fraction (<300 nucleotides) was hybridized on a μParaflo Microfluidic chip containing detection probes for all mouse microRNAs (miRNAs) in the miRBase version-17 (miRBase, http://microrna.sanger.ac. uk/sequences). The hybridized microarray chips were labeled with fluorescent dyes and laser scanned to obtain fluorescent images. The signal values for each sample were derived by background subtraction and normalization. Microarray chip hybridization, fluorescent labeling, laser scanning, and background subtraction and normalization were performed by LC Sciences proprietary method.
Scan protocol The small RNA fraction (<300 nucleotides) was hybridized on a μParaflo Microfluidic chip containing detection probes for all mouse microRNAs (miRNAs) in the miRBase version-17 (miRBase, http://microrna.sanger.ac. uk/sequences). The hybridized microarray chips were labeled with fluorescent dyes and laser scanned to obtain fluorescent images. The signal values for each sample were derived by background subtraction and normalization. Microarray chip hybridization, fluorescent labeling, laser scanning, and background subtraction and normalization were performed by LC Sciences proprietary method.
Data processing The signal values from each of the five age groups (P2, P7, P14, P35) were averaged, and the P values using One-way ANOVA were calculated. The differentially detected signals are defined by P < 0.05.
 
Submission date Jul 18, 2022
Last update date Jul 19, 2022
Contact name harini ramalingam
E-mail(s) harini.ramalingam@utsouthwestern.edu
Phone 9727301211
Organization name UTSW
Department IMN
Lab F5.206
Street address 5323 Harry Hines Boulevard
City Dallas
State/province Texas
ZIP/Postal code 75390
Country USA
 
Platform ID GPL32491
Series (1)
GSE208429 miRNA expression in kidneys

Data table header descriptions
ID_REF
VALUE signal

Data table
ID_REF VALUE
328 957.1484063
378 1288.825535
332 452.3180721
330 34.70588836
64 159.3890131
264 850.0393322
406 1108.911794
224 3094.78258
121 612.8418149
179 1739.722622
283 1131.405402
359 2668.256066
23 842.2719172
114 1253.279804
665 1631.343393
459 6138.533197
29 11034.68138
27 8288.034095
247 1303.131352
44 59.57334053

Total number of rows: 501

Table truncated, full table size 7 Kbytes.




Supplementary data files not provided
Processed data are available on Series record

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