Human Skin miRNA Search Results


96
Thermo Fisher taqman advanced mirna cdna synthesis kit
Taqman Advanced Mirna Cdna Synthesis Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Qiagen paxgene tissue mirna kit
Paxgene Tissue Mirna Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Agilent technologies micro rna isolation kit
Micro Rna Isolation Kit, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Qiagen miscript mirna pcr array
Differentially expressed <t>miRNA</t> in cALD (grey) and AMN (white) fibroblasts from miRNome miRNA <t>PCR</t> array. The expression of 1008 most abundantly expressed and best characterized miRNA sequences in the human miRNA genome was profiled using Human miRNome miRNA PCR array (Qiagen-MIHS-216Z) in triplicate. The relative expression was calculated using the ΔΔCT method and is presented as fold change relative to control. Among 1008 miRNAs, 11 miRNAs were significantly differentially regulated between cALD and AMN as shown in the figure. miR-196a was most significantly differentially regulated
Miscript Mirna Pcr Array, supplied by Qiagen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/miscript mirna pcr array/product/Qiagen
Average 90 stars, based on 1 article reviews
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Qiagen irneasy ffpe kit
Differentially expressed <t>miRNA</t> in cALD (grey) and AMN (white) fibroblasts from miRNome miRNA <t>PCR</t> array. The expression of 1008 most abundantly expressed and best characterized miRNA sequences in the human miRNA genome was profiled using Human miRNome miRNA PCR array (Qiagen-MIHS-216Z) in triplicate. The relative expression was calculated using the ΔΔCT method and is presented as fold change relative to control. Among 1008 miRNAs, 11 miRNAs were significantly differentially regulated between cALD and AMN as shown in the figure. miR-196a was most significantly differentially regulated
Irneasy Ffpe Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/irneasy ffpe kit/product/Qiagen
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Qiagen mouse skin tissue
Differentially expressed <t>miRNA</t> in cALD (grey) and AMN (white) fibroblasts from miRNome miRNA <t>PCR</t> array. The expression of 1008 most abundantly expressed and best characterized miRNA sequences in the human miRNA genome was profiled using Human miRNome miRNA PCR array (Qiagen-MIHS-216Z) in triplicate. The relative expression was calculated using the ΔΔCT method and is presented as fold change relative to control. Among 1008 miRNAs, 11 miRNAs were significantly differentially regulated between cALD and AMN as shown in the figure. miR-196a was most significantly differentially regulated
Mouse Skin Tissue, supplied by Qiagen, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
Thermo Fisher human c ski
Differentially expressed <t>miRNA</t> in cALD (grey) and AMN (white) fibroblasts from miRNome miRNA <t>PCR</t> array. The expression of 1008 most abundantly expressed and best characterized miRNA sequences in the human miRNA genome was profiled using Human miRNome miRNA PCR array (Qiagen-MIHS-216Z) in triplicate. The relative expression was calculated using the ΔΔCT method and is presented as fold change relative to control. Among 1008 miRNAs, 11 miRNAs were significantly differentially regulated between cALD and AMN as shown in the figure. miR-196a was most significantly differentially regulated
Human C Ski, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
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N/A
GeneCopoeia offers genome-wide human, mouse and rat microRNA (miRNA) 3′ UTR target clones in mammalian expression vectors. miRNA 3′ UTR target clones can be used for miRNA target identification and functional validation of predicted targets,
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N/A
GeneCopoeia offers genome-wide human, mouse and rat microRNA (miRNA) 3′ UTR target clones in mammalian expression vectors. miRNA 3′ UTR target clones can be used for miRNA target identification and functional validation of predicted targets,
  Buy from Supplier

N/A
GeneCopoeia offers genome-wide human, mouse and rat microRNA (miRNA) 3′ UTR target clones in mammalian expression vectors. miRNA 3′ UTR target clones can be used for miRNA target identification and functional validation of predicted targets,
  Buy from Supplier

N/A
GeneCopoeia offers genome-wide human, mouse and rat microRNA (miRNA) 3′ UTR target clones in mammalian expression vectors. miRNA 3′ UTR target clones can be used for miRNA target identification and functional validation of predicted targets,
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Image Search Results


Differentially expressed miRNA in cALD (grey) and AMN (white) fibroblasts from miRNome miRNA PCR array. The expression of 1008 most abundantly expressed and best characterized miRNA sequences in the human miRNA genome was profiled using Human miRNome miRNA PCR array (Qiagen-MIHS-216Z) in triplicate. The relative expression was calculated using the ΔΔCT method and is presented as fold change relative to control. Among 1008 miRNAs, 11 miRNAs were significantly differentially regulated between cALD and AMN as shown in the figure. miR-196a was most significantly differentially regulated

Journal: Molecular neurobiology

Article Title: MicroRNA Profiling Identifies miR-196a as Differentially Expressed in Childhood Adrenoleukodystrophy and Adult Adrenomyeloneuropathy

doi: 10.1007/s12035-016-9746-0

Figure Lengend Snippet: Differentially expressed miRNA in cALD (grey) and AMN (white) fibroblasts from miRNome miRNA PCR array. The expression of 1008 most abundantly expressed and best characterized miRNA sequences in the human miRNA genome was profiled using Human miRNome miRNA PCR array (Qiagen-MIHS-216Z) in triplicate. The relative expression was calculated using the ΔΔCT method and is presented as fold change relative to control. Among 1008 miRNAs, 11 miRNAs were significantly differentially regulated between cALD and AMN as shown in the figure. miR-196a was most significantly differentially regulated

Article Snippet: To examine the possible role of microRNA (miRNA) in X-ALD disease mechanisms for differences in cALD and AMN phenotype, we profiled 1008 known miRNA in cALD, AMN, and normal human skin fibroblasts using miScript miRNA PCR array (Qiagen) and selected miRNAs which had differential expression in cALD and AMN fibroblasts.

Techniques: Expressing

Validation of miR-196a expression in human skin fibroblasts (a) and human brain samples (b) by qRT-PCR. miR-196a expression was validated in human skin fibroblasts and human brain samples (from equivalent brain regions) using Qiagen miScript primer assays by qRT-PCR. The values were normalized to SNORD61 and presented as fold change. As represented by figure, miR-196a expression was downregulated in cALD fibroblasts and brain samples and upregulated in AMN fibroblasts and brain samples. B3 is brain sample from AMN that subsequently developed CNS disease. Downregulation of miR-196a expression in brain sample B3 indicates of cerebral involvement. Thirty-five percent of AMN patients develop cerebral involvement

Journal: Molecular neurobiology

Article Title: MicroRNA Profiling Identifies miR-196a as Differentially Expressed in Childhood Adrenoleukodystrophy and Adult Adrenomyeloneuropathy

doi: 10.1007/s12035-016-9746-0

Figure Lengend Snippet: Validation of miR-196a expression in human skin fibroblasts (a) and human brain samples (b) by qRT-PCR. miR-196a expression was validated in human skin fibroblasts and human brain samples (from equivalent brain regions) using Qiagen miScript primer assays by qRT-PCR. The values were normalized to SNORD61 and presented as fold change. As represented by figure, miR-196a expression was downregulated in cALD fibroblasts and brain samples and upregulated in AMN fibroblasts and brain samples. B3 is brain sample from AMN that subsequently developed CNS disease. Downregulation of miR-196a expression in brain sample B3 indicates of cerebral involvement. Thirty-five percent of AMN patients develop cerebral involvement

Article Snippet: To examine the possible role of microRNA (miRNA) in X-ALD disease mechanisms for differences in cALD and AMN phenotype, we profiled 1008 known miRNA in cALD, AMN, and normal human skin fibroblasts using miScript miRNA PCR array (Qiagen) and selected miRNAs which had differential expression in cALD and AMN fibroblasts.

Techniques: Expressing, Quantitative RT-PCR

Roles of miR-196a in target gene expression. To establish the regulation of target genes by miR-196a, miR-196a mimic was transfected in ABCD1 knockdown U87 astrocytes cells (U87 Lenti) and transfection efficiency evaluated by miScript qRT-PCR. SNORD61 was used as an internal control and represented as miR-196a/SNORD61 (a). The expression of target genes IKKα and IKKβ was analysed after the transfection of miR-196a mimic and normalized to GAPDH. The expression of these genes was significantly increased in ABCD1 silenced cells as compared to wild type but significantly decreased after transfection of mimic in U87 Lenti cells (b and c). **P < 0.05. An unpaired student t test was used to determine the statistical significance of the data from three independent experiments

Journal: Molecular neurobiology

Article Title: MicroRNA Profiling Identifies miR-196a as Differentially Expressed in Childhood Adrenoleukodystrophy and Adult Adrenomyeloneuropathy

doi: 10.1007/s12035-016-9746-0

Figure Lengend Snippet: Roles of miR-196a in target gene expression. To establish the regulation of target genes by miR-196a, miR-196a mimic was transfected in ABCD1 knockdown U87 astrocytes cells (U87 Lenti) and transfection efficiency evaluated by miScript qRT-PCR. SNORD61 was used as an internal control and represented as miR-196a/SNORD61 (a). The expression of target genes IKKα and IKKβ was analysed after the transfection of miR-196a mimic and normalized to GAPDH. The expression of these genes was significantly increased in ABCD1 silenced cells as compared to wild type but significantly decreased after transfection of mimic in U87 Lenti cells (b and c). **P < 0.05. An unpaired student t test was used to determine the statistical significance of the data from three independent experiments

Article Snippet: To examine the possible role of microRNA (miRNA) in X-ALD disease mechanisms for differences in cALD and AMN phenotype, we profiled 1008 known miRNA in cALD, AMN, and normal human skin fibroblasts using miScript miRNA PCR array (Qiagen) and selected miRNAs which had differential expression in cALD and AMN fibroblasts.

Techniques: Expressing, Transfection, Quantitative RT-PCR