Dme-mir-7 is a specific miRNA assay control for Drosophila melanogaster (D. melanogaster) [PMC6224079]. It was used in a pilot run to confirm the absence of plant/insect miRNA contamination and unspecific amplifications in serum samples [PMC6224079]. Dme-mir-7 was also included in a Taqman Low-Density Array (TLDA) card for qPCR analysis of mature human miRNAs [PMC6224079]. In a study comparing different miRNAs, dme-mir-7 was found to have 5325 recovered regions, with the SBM method returning 28 [PMC2365947]. The dme-mir-7 results showed an average of 273 sequences scoring equal to or better than the left-out sequences and an average of 8868 sequences scoring at least as high as the validated target using miRanda [PMC2365947]. In another study, dme-mir-7 was used as a spike-in RNA for RNA isolation and reverse transcription in serum samples [PMC8615628]. It was also found to be significantly down-regulated in SSc-A-MSCs compared to HC-A-MSCs, with a fold change less than 0.5 [PMC6509164]. The cDNA synthesized from total RNA using dme-mir-7 RT-primer was used for TaqMan MicroRNA Assay analysis [PMC4273950].
u U U U U uggu u gagugcau ccgua GGAAGAC AG GAUUU GUUGUu c u |||||||| ||||| ||||||| || ||||| |||||| | uuuacgug ggcAU UCUUCUG UC CUAAA UAACaa g u c - U C - uaau g
Accession | MIMAT0000112 |
Description | Drosophila melanogaster dme-miR-7-5p mature miRNA |
Sequence | 15 - UGGAAGACUAGUGAUUUUGUUGU - 37 |
Evidence |
experimental
cloned [1,4], Northern [1,3-4], 454 [5-6], Illumina [6] |
Database links | |
Predicted targets |
Accession | MIMAT0020790 |
Description | Drosophila melanogaster dme-miR-7-3p mature miRNA |
Sequence | 55 - CAAUAAAUCCCUUGUCUUCUUA - 76 |
Evidence | not_experimental |
Database links |
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