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Sample GSM6346279 Query DataSets for GSM6346279
Status Public on Jul 19, 2022
Title Postnatal day 0 kidney 4
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
328 258.4278131
378 9263.802188
332 155.3521172
330 15.22396993
64 1260.752766
264 4233.430918
406 328.7324271
224 16539.12973
121 2669.405187
179 955.6592156
283 699.9289683
359 6542.836879
23 3977.639451
114 7069.417229
665 2113.482193
459 2230.146163
29 16982.36046
27 17560.68116
247 7660.336385
44 318.8720347

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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