mouse v4.0 lncrna microarray Search Results


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Arraystar inc human lncrna microarray v4.0
Transcriptome analysis identifies p53 signaling as the most significantly upregulated pathway upon Meg3 knockdown. HUVECs were transfected with control or Meg3 GapmeRs. 24 h after transfection, cells were treated with 10 ng/ml TNF-α for 3 h and collected for <t>microarray</t> gene chip analysis. Chromatin immunoprecipitation was performed using transfected cells with or without 10 ng/ml TNF-α treatment for 1 h. ( A ) Volcano plot shows differentially expressed mRNAs in ECs upon Meg3 knockdown. ( B ) KEGG signaling pathways analysis identified significantly regulated pathways among upregulated genes upon Meg3 knockdown. ( C ) Venn diagram shows p53 target genes that are regulated by Meg3. ( D ) qPCR analysis of a group of p53 target genes that were induced upon Meg3 knockdown. (E) Enrichment of p53 at the promoters of indicated genes was identified by chromatin immunoprecipitation using anti-p53 antibodies followed by qPCR analysis. Data show mean ± S.E.M., n = 3; * P < 0.05.
Human Lncrna Microarray V4.0, supplied by Arraystar inc, 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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Arraystar inc mouse lncrna microarray v4.0
Transcriptome analysis identifies p53 signaling as the most significantly upregulated pathway upon Meg3 knockdown. HUVECs were transfected with control or Meg3 GapmeRs. 24 h after transfection, cells were treated with 10 ng/ml TNF-α for 3 h and collected for <t>microarray</t> gene chip analysis. Chromatin immunoprecipitation was performed using transfected cells with or without 10 ng/ml TNF-α treatment for 1 h. ( A ) Volcano plot shows differentially expressed mRNAs in ECs upon Meg3 knockdown. ( B ) KEGG signaling pathways analysis identified significantly regulated pathways among upregulated genes upon Meg3 knockdown. ( C ) Venn diagram shows p53 target genes that are regulated by Meg3. ( D ) qPCR analysis of a group of p53 target genes that were induced upon Meg3 knockdown. (E) Enrichment of p53 at the promoters of indicated genes was identified by chromatin immunoprecipitation using anti-p53 antibodies followed by qPCR analysis. Data show mean ± S.E.M., n = 3; * P < 0.05.
Mouse Lncrna Microarray V4.0, supplied by Arraystar inc, 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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CapitalBio Corporation human lncrna microarray v4.0
Differentially expressed lncRNAs and mRNAs between obese and non-obese participants were subjected to hierarchical clustering. The color scale on the top illustrates the relative expression level of lncRNAs across all samples. Red color indicates high relative expression and green color indicates low relative expression. ( A ) <t>lncRNA;</t> ( B ) mRNA.
Human Lncrna Microarray V4.0, supplied by CapitalBio Corporation, 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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CapitalBio Corporation gene expression chip lncrna + mrna human gene expression microarray v4.0
Differentially expressed lncRNAs and mRNAs between obese and non-obese participants were subjected to hierarchical clustering. The color scale on the top illustrates the relative expression level of lncRNAs across all samples. Red color indicates high relative expression and green color indicates low relative expression. ( A ) <t>lncRNA;</t> ( B ) mRNA.
Gene Expression Chip Lncrna + Mrna Human Gene Expression Microarray V4.0, supplied by CapitalBio Corporation, 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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Differentially expressed lncRNAs and mRNAs between obese and non-obese participants were subjected to hierarchical clustering. The color scale on the top illustrates the relative expression level of lncRNAs across all samples. Red color indicates high relative expression and green color indicates low relative expression. ( A ) <t>lncRNA;</t> ( B ) mRNA.
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Differentially expressed lncRNAs and mRNAs between obese and non-obese participants were subjected to hierarchical clustering. The color scale on the top illustrates the relative expression level of lncRNAs across all samples. Red color indicates high relative expression and green color indicates low relative expression. ( A ) <t>lncRNA;</t> ( B ) mRNA.
Arraystar Human Lncrna Microarray V4.0, supplied by KangChen Inc, 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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Relative expression of lncRNAs. ( A, B ) The raw images of the <t>microarray</t> analysis were shown; ( C ) the scatter plot was shown; ( D ) The comparison of relative expression of NRAD1 in HCC and normal cell lines; ( E ) The comparison of relative expression of LINC00152 in HCC and normal cell lines.
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Arraystar inc human lncrna v4.0 analysis
Elevated expression of <t>lncRNA</t> URAHP in preeclampsia placenta tissues. (A and B) Differentially expressed lncRNAs or mRNA in 3 pairs of placental tissues from women with PE and normal pregnancy (Con). (C) The Transcriptional expression of lncRNA URAHP in placental tissues from women with PE and normal pregnancy (Con) examined by real-time PCR, and (D) indicates lncRNA URAHP in HTR-8/SVneo, JAR and JEG-3 cell lines. All the experiments were carried out for three times. *P < 0.05; **P < 0.01. β-actin was used as a loading control.
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Elevated expression of <t>lncRNA</t> URAHP in preeclampsia placenta tissues. (A and B) Differentially expressed lncRNAs or mRNA in 3 pairs of placental tissues from women with PE and normal pregnancy (Con). (C) The Transcriptional expression of lncRNA URAHP in placental tissues from women with PE and normal pregnancy (Con) examined by real-time PCR, and (D) indicates lncRNA URAHP in HTR-8/SVneo, JAR and JEG-3 cell lines. All the experiments were carried out for three times. *P < 0.05; **P < 0.01. β-actin was used as a loading control.
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Elevated expression of <t>lncRNA</t> URAHP in preeclampsia placenta tissues. (A and B) Differentially expressed lncRNAs or mRNA in 3 pairs of placental tissues from women with PE and normal pregnancy (Con). (C) The Transcriptional expression of lncRNA URAHP in placental tissues from women with PE and normal pregnancy (Con) examined by real-time PCR, and (D) indicates lncRNA URAHP in HTR-8/SVneo, JAR and JEG-3 cell lines. All the experiments were carried out for three times. *P < 0.05; **P < 0.01. β-actin was used as a loading control.
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Elevated expression of <t>lncRNA</t> URAHP in preeclampsia placenta tissues. (A and B) Differentially expressed lncRNAs or mRNA in 3 pairs of placental tissues from women with PE and normal pregnancy (Con). (C) The Transcriptional expression of lncRNA URAHP in placental tissues from women with PE and normal pregnancy (Con) examined by real-time PCR, and (D) indicates lncRNA URAHP in HTR-8/SVneo, JAR and JEG-3 cell lines. All the experiments were carried out for three times. *P < 0.05; **P < 0.01. β-actin was used as a loading control.
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Elevated expression of <t>lncRNA</t> URAHP in preeclampsia placenta tissues. (A and B) Differentially expressed lncRNAs or mRNA in 3 pairs of placental tissues from women with PE and normal pregnancy (Con). (C) The Transcriptional expression of lncRNA URAHP in placental tissues from women with PE and normal pregnancy (Con) examined by real-time PCR, and (D) indicates lncRNA URAHP in HTR-8/SVneo, JAR and JEG-3 cell lines. All the experiments were carried out for three times. *P < 0.05; **P < 0.01. β-actin was used as a loading control.
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Image Search Results


Transcriptome analysis identifies p53 signaling as the most significantly upregulated pathway upon Meg3 knockdown. HUVECs were transfected with control or Meg3 GapmeRs. 24 h after transfection, cells were treated with 10 ng/ml TNF-α for 3 h and collected for microarray gene chip analysis. Chromatin immunoprecipitation was performed using transfected cells with or without 10 ng/ml TNF-α treatment for 1 h. ( A ) Volcano plot shows differentially expressed mRNAs in ECs upon Meg3 knockdown. ( B ) KEGG signaling pathways analysis identified significantly regulated pathways among upregulated genes upon Meg3 knockdown. ( C ) Venn diagram shows p53 target genes that are regulated by Meg3. ( D ) qPCR analysis of a group of p53 target genes that were induced upon Meg3 knockdown. (E) Enrichment of p53 at the promoters of indicated genes was identified by chromatin immunoprecipitation using anti-p53 antibodies followed by qPCR analysis. Data show mean ± S.E.M., n = 3; * P < 0.05.

Journal: Nucleic Acids Research

Article Title: LncRNA Meg3 protects endothelial function by regulating the DNA damage response

doi: 10.1093/nar/gky1190

Figure Lengend Snippet: Transcriptome analysis identifies p53 signaling as the most significantly upregulated pathway upon Meg3 knockdown. HUVECs were transfected with control or Meg3 GapmeRs. 24 h after transfection, cells were treated with 10 ng/ml TNF-α for 3 h and collected for microarray gene chip analysis. Chromatin immunoprecipitation was performed using transfected cells with or without 10 ng/ml TNF-α treatment for 1 h. ( A ) Volcano plot shows differentially expressed mRNAs in ECs upon Meg3 knockdown. ( B ) KEGG signaling pathways analysis identified significantly regulated pathways among upregulated genes upon Meg3 knockdown. ( C ) Venn diagram shows p53 target genes that are regulated by Meg3. ( D ) qPCR analysis of a group of p53 target genes that were induced upon Meg3 knockdown. (E) Enrichment of p53 at the promoters of indicated genes was identified by chromatin immunoprecipitation using anti-p53 antibodies followed by qPCR analysis. Data show mean ± S.E.M., n = 3; * P < 0.05.

Article Snippet: Arraystar Human LncRNA Microarray v4.0, performed by Arraystar Inc. (Rockville, MD, USA), is designed for the global expression profiling of 40 173 human lncRNA and 20,730 protein-coding mRNA transcripts.

Techniques: Knockdown, Transfection, Control, Microarray, Chromatin Immunoprecipitation, Protein-Protein interactions

LncRNA pull-down assay identifies PTBP3 as a binding partner of Meg3. ( A ) LncRNA pull-down assay was used to identify the proteins associated with Meg3 transcript variant 1 (TV1) by incubating the cell lysates with biotinylated sense or antisense Meg3 RNA. The RNA–protein complexes captured by T-1 beads were subjected to silver stain after separation on SDS-PAGE gel. ( B ) The RNA–protein complexes from lncRNA pulldown using antisense Meg3 (negative control RNA), sense Meg3 (TV1), and Meg3 deletion mutants were subjected to western blot analysis of PTBP3 and GAPDH after separation on SDS-PAGE gel. GAPDH was examined as a negative control protein. ( C ) The interaction of endogenous PTBP3 with Meg3 was detected by RNA immunoprecipitation. EC lysates were immunoprecipitated with anti-PTBP3 antibody or Isotype matched control IgG. Meg3 was examined by qPCR in the immuno-precipitates using primer set 2 as shown in (D). LncRNA Neat1 was used as a positive control RNA that interacts with PTBP3. ( D ) Different sets of Meg3 primers were used to detect Meg3 by qPCR following RNA immunoprecipitation using anti-PTBP3 antibodies. Primer sets 1, 2, 5 detect Meg3 transcript variants 1 and 6 (TV1 and TV6); primer sets 3 and 4 detect Meg3 TV1; and primer sets 6 and 7 detect Meg3 TV6. ( E ) Dual-staining of Meg3 and PTBP3 in HUVECs. Linear trajectories (yellow line) crossing the cells with the intensities of Meg3 and PTBP3 signals were presented at the right side of images. White and black arrows indicate partial colocalization of Meg3 and PTBP3 in the nucleus of HUVECs. Data show mean ± S.E.M., n = 3; * P < 0.05.

Journal: Nucleic Acids Research

Article Title: LncRNA Meg3 protects endothelial function by regulating the DNA damage response

doi: 10.1093/nar/gky1190

Figure Lengend Snippet: LncRNA pull-down assay identifies PTBP3 as a binding partner of Meg3. ( A ) LncRNA pull-down assay was used to identify the proteins associated with Meg3 transcript variant 1 (TV1) by incubating the cell lysates with biotinylated sense or antisense Meg3 RNA. The RNA–protein complexes captured by T-1 beads were subjected to silver stain after separation on SDS-PAGE gel. ( B ) The RNA–protein complexes from lncRNA pulldown using antisense Meg3 (negative control RNA), sense Meg3 (TV1), and Meg3 deletion mutants were subjected to western blot analysis of PTBP3 and GAPDH after separation on SDS-PAGE gel. GAPDH was examined as a negative control protein. ( C ) The interaction of endogenous PTBP3 with Meg3 was detected by RNA immunoprecipitation. EC lysates were immunoprecipitated with anti-PTBP3 antibody or Isotype matched control IgG. Meg3 was examined by qPCR in the immuno-precipitates using primer set 2 as shown in (D). LncRNA Neat1 was used as a positive control RNA that interacts with PTBP3. ( D ) Different sets of Meg3 primers were used to detect Meg3 by qPCR following RNA immunoprecipitation using anti-PTBP3 antibodies. Primer sets 1, 2, 5 detect Meg3 transcript variants 1 and 6 (TV1 and TV6); primer sets 3 and 4 detect Meg3 TV1; and primer sets 6 and 7 detect Meg3 TV6. ( E ) Dual-staining of Meg3 and PTBP3 in HUVECs. Linear trajectories (yellow line) crossing the cells with the intensities of Meg3 and PTBP3 signals were presented at the right side of images. White and black arrows indicate partial colocalization of Meg3 and PTBP3 in the nucleus of HUVECs. Data show mean ± S.E.M., n = 3; * P < 0.05.

Article Snippet: Arraystar Human LncRNA Microarray v4.0, performed by Arraystar Inc. (Rockville, MD, USA), is designed for the global expression profiling of 40 173 human lncRNA and 20,730 protein-coding mRNA transcripts.

Techniques: Pull Down Assay, Binding Assay, Variant Assay, Silver Staining, SDS Page, Negative Control, Western Blot, RNA Immunoprecipitation, Immunoprecipitation, Control, Positive Control, Staining

Differentially expressed lncRNAs and mRNAs between obese and non-obese participants were subjected to hierarchical clustering. The color scale on the top illustrates the relative expression level of lncRNAs across all samples. Red color indicates high relative expression and green color indicates low relative expression. ( A ) lncRNA; ( B ) mRNA.

Journal: Scientific Reports

Article Title: Differentially expressed circulating LncRNAs and mRNA identified by microarray analysis in obese patients

doi: 10.1038/srep35421

Figure Lengend Snippet: Differentially expressed lncRNAs and mRNAs between obese and non-obese participants were subjected to hierarchical clustering. The color scale on the top illustrates the relative expression level of lncRNAs across all samples. Red color indicates high relative expression and green color indicates low relative expression. ( A ) lncRNA; ( B ) mRNA.

Article Snippet: We performed microarray profiling using Human LncRNA Microarray V4.0 (CapitalBio Corp, Beijing, China), including 34,235 mRNAs and 40,914 lncRNAs.

Techniques: Expressing

Expression of lncRNA-p5549, lncRNA-p21015 and lncRNA-p19461 was detected by qPCR and normalized by U6 expression. (**P < 0.01)

Journal: Scientific Reports

Article Title: Differentially expressed circulating LncRNAs and mRNA identified by microarray analysis in obese patients

doi: 10.1038/srep35421

Figure Lengend Snippet: Expression of lncRNA-p5549, lncRNA-p21015 and lncRNA-p19461 was detected by qPCR and normalized by U6 expression. (**P < 0.01)

Article Snippet: We performed microarray profiling using Human LncRNA Microarray V4.0 (CapitalBio Corp, Beijing, China), including 34,235 mRNAs and 40,914 lncRNAs.

Techniques: Expressing

Correlation between lncRNAs concentrations and studied variables in the cross-sectional study Data are R ( p ).

Journal: Scientific Reports

Article Title: Differentially expressed circulating LncRNAs and mRNA identified by microarray analysis in obese patients

doi: 10.1038/srep35421

Figure Lengend Snippet: Correlation between lncRNAs concentrations and studied variables in the cross-sectional study Data are R ( p ).

Article Snippet: We performed microarray profiling using Human LncRNA Microarray V4.0 (CapitalBio Corp, Beijing, China), including 34,235 mRNAs and 40,914 lncRNAs.

Techniques:

Clinical characteristics of subjects included in longitudinal studies.

Journal: Scientific Reports

Article Title: Differentially expressed circulating LncRNAs and mRNA identified by microarray analysis in obese patients

doi: 10.1038/srep35421

Figure Lengend Snippet: Clinical characteristics of subjects included in longitudinal studies.

Article Snippet: We performed microarray profiling using Human LncRNA Microarray V4.0 (CapitalBio Corp, Beijing, China), including 34,235 mRNAs and 40,914 lncRNAs.

Techniques:

Baseline and diet-induced weight loss levels of lncRNA-p5549 ( A ) lncRNA-p21015 ( B ) and lncRNA-p19461 ( C ) in obese participants. **P <0.01. Date are shown as mean (SD).

Journal: Scientific Reports

Article Title: Differentially expressed circulating LncRNAs and mRNA identified by microarray analysis in obese patients

doi: 10.1038/srep35421

Figure Lengend Snippet: Baseline and diet-induced weight loss levels of lncRNA-p5549 ( A ) lncRNA-p21015 ( B ) and lncRNA-p19461 ( C ) in obese participants. **P <0.01. Date are shown as mean (SD).

Article Snippet: We performed microarray profiling using Human LncRNA Microarray V4.0 (CapitalBio Corp, Beijing, China), including 34,235 mRNAs and 40,914 lncRNAs.

Techniques:

Relative expression of lncRNAs. ( A, B ) The raw images of the microarray analysis were shown; ( C ) the scatter plot was shown; ( D ) The comparison of relative expression of NRAD1 in HCC and normal cell lines; ( E ) The comparison of relative expression of LINC00152 in HCC and normal cell lines.

Journal: OncoTargets and therapy

Article Title: Long Non-Coding RNA NRAD1 and LINC00152 are Highly Expressed and Associated with Prognosis in Patients with Hepatocellular Carcinoma

doi: 10.2147/OTT.S251231

Figure Lengend Snippet: Relative expression of lncRNAs. ( A, B ) The raw images of the microarray analysis were shown; ( C ) the scatter plot was shown; ( D ) The comparison of relative expression of NRAD1 in HCC and normal cell lines; ( E ) The comparison of relative expression of LINC00152 in HCC and normal cell lines.

Article Snippet: We performed LncRNA and mRNA human gene expression microarray V4.0 (Capitalbio, 4×180K, two-channel, containing about 37 thousand lncRNAs and 34 thousand mRNAs) was applied to the profiling of lncRNAs in four cancerous tissues and the paired paracancerous tissues.

Techniques: Expressing, Microarray, Comparison

Elevated expression of lncRNA URAHP in preeclampsia placenta tissues. (A and B) Differentially expressed lncRNAs or mRNA in 3 pairs of placental tissues from women with PE and normal pregnancy (Con). (C) The Transcriptional expression of lncRNA URAHP in placental tissues from women with PE and normal pregnancy (Con) examined by real-time PCR, and (D) indicates lncRNA URAHP in HTR-8/SVneo, JAR and JEG-3 cell lines. All the experiments were carried out for three times. *P < 0.05; **P < 0.01. β-actin was used as a loading control.

Journal: American Journal of Translational Research

Article Title: The pseudogene URAHP promotes proliferation and regulates the pathogenesis of preeclampsia

doi:

Figure Lengend Snippet: Elevated expression of lncRNA URAHP in preeclampsia placenta tissues. (A and B) Differentially expressed lncRNAs or mRNA in 3 pairs of placental tissues from women with PE and normal pregnancy (Con). (C) The Transcriptional expression of lncRNA URAHP in placental tissues from women with PE and normal pregnancy (Con) examined by real-time PCR, and (D) indicates lncRNA URAHP in HTR-8/SVneo, JAR and JEG-3 cell lines. All the experiments were carried out for three times. *P < 0.05; **P < 0.01. β-actin was used as a loading control.

Article Snippet: The sample preparation and microarray hybridization were performed according to the manufacturer’s standard protocols with minor modifications (Arraystar Human LncRNA V4.0 analysis) [ 17 ].

Techniques: Expressing, Real-time Polymerase Chain Reaction, Control