rat lncrna microarray Search Results


90
Arraystar inc rat lncrna microarray
Rat Lncrna Microarray, 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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rat lncrna microarray - by Bioz Stars, 2026-04
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Ribobio co riboarray microarray covering 29,659 unique rat mrnas and 6713 unique rat lncrnas (refseq60)
The expression profile analysis of the lncRNAs/mRNAs and overview of <t>microarray</t> analysis. The purity and quantity of RNA were evaluated by a K5500 micro-spectrophotometer. RNA purity was acceptable if A260/A230 ≥ 0.5 and A260/A280 ≥ 1.5. RNA integrity was acceptable when RIN value ≥ 7 detected by Agilent 2200 RNA assay. Gel electrophoresis ( A ) was conducted to assess the genomic DNA contamination. Expression signal distribution after every mRNA array dataset was normalized ( B ). The microarray heat map of spinal dorsal horn tissues in the PHN model and analysis of differentially expressed lncRNAs (Vehicle group: A1, A2 and A3; PHN model group: B1, B2 and B3) ( C and D ). Red color represented that the relative expression was high and green color represented that the relative expression was low. For advanced data analysis, all biological replicates were pooled and calculated to identify differentially expressed mRNAs based on the threshold of |Fold change| ≥ 1.5 and P ≤ 0.05. Unsupervised hierarchical clustering analysis was conducted to demonstrate the correlation of expression profiles between treatment and biological replicates.
Riboarray Microarray Covering 29,659 Unique Rat Mrnas And 6713 Unique Rat Lncrnas (Refseq60), supplied by Ribobio co, 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/riboarray microarray covering 29,659 unique rat mrnas and 6713 unique rat lncrnas (refseq60)/product/Ribobio co
Average 90 stars, based on 1 article reviews
riboarray microarray covering 29,659 unique rat mrnas and 6713 unique rat lncrnas (refseq60) - by Bioz Stars, 2026-04
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Arraystar inc aglient rat lncrna microarray v2.0
lncRNAs regulated by nucleolin in cardiomyocytes. (A) Heatmap profile of <t>lncRNA</t> <t>microarray</t> analysis. Green to red colors indicate low to high transcriptional levels. The lncRNAs differentially expressed between the two groups were identified through paired t-test P ≤ 0.05 and a fold change (FC) ≥ 2.5; n = 3 independent biological samples for each group. (B) The expression of 15 selected lncRNAs in chip test, where 10 differentially expressed up-regulated lncRNAs (up) and 5 differentially expressed down-regulated lncRNAs (down) were selected. (C) The interactions between nucleolin and lncRNAs were confirmed by RIP and identified via qRT-PCR. *, P < 0.05, vs. IgG group, n = 3. pcDNA3.1, the empty vector served as negative control; pcDNA3.1-Nuc, overexpression nucleolin group. (D) Bioinformatics website predicted Fendrr binding elements with nucleolin.
Aglient Rat Lncrna Microarray V2.0, 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
https://www.bioz.com/result/aglient rat lncrna microarray v2.0/product/Arraystar inc
Average 90 stars, based on 1 article reviews
aglient rat lncrna microarray v2.0 - by Bioz Stars, 2026-04
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Arraystar inc sd rat lncrna/mrna expression microarray v3.0 (8 × 60 k)
lncRNAs regulated by nucleolin in cardiomyocytes. (A) Heatmap profile of <t>lncRNA</t> <t>microarray</t> analysis. Green to red colors indicate low to high transcriptional levels. The lncRNAs differentially expressed between the two groups were identified through paired t-test P ≤ 0.05 and a fold change (FC) ≥ 2.5; n = 3 independent biological samples for each group. (B) The expression of 15 selected lncRNAs in chip test, where 10 differentially expressed up-regulated lncRNAs (up) and 5 differentially expressed down-regulated lncRNAs (down) were selected. (C) The interactions between nucleolin and lncRNAs were confirmed by RIP and identified via qRT-PCR. *, P < 0.05, vs. IgG group, n = 3. pcDNA3.1, the empty vector served as negative control; pcDNA3.1-Nuc, overexpression nucleolin group. (D) Bioinformatics website predicted Fendrr binding elements with nucleolin.
Sd Rat Lncrna/Mrna Expression Microarray V3.0 (8 × 60 K), 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
https://www.bioz.com/result/sd rat lncrna/mrna expression microarray v3.0 (8 × 60 k)/product/Arraystar inc
Average 90 stars, based on 1 article reviews
sd rat lncrna/mrna expression microarray v3.0 (8 × 60 k) - by Bioz Stars, 2026-04
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The expression profile analysis of the lncRNAs/mRNAs and overview of microarray analysis. The purity and quantity of RNA were evaluated by a K5500 micro-spectrophotometer. RNA purity was acceptable if A260/A230 ≥ 0.5 and A260/A280 ≥ 1.5. RNA integrity was acceptable when RIN value ≥ 7 detected by Agilent 2200 RNA assay. Gel electrophoresis ( A ) was conducted to assess the genomic DNA contamination. Expression signal distribution after every mRNA array dataset was normalized ( B ). The microarray heat map of spinal dorsal horn tissues in the PHN model and analysis of differentially expressed lncRNAs (Vehicle group: A1, A2 and A3; PHN model group: B1, B2 and B3) ( C and D ). Red color represented that the relative expression was high and green color represented that the relative expression was low. For advanced data analysis, all biological replicates were pooled and calculated to identify differentially expressed mRNAs based on the threshold of |Fold change| ≥ 1.5 and P ≤ 0.05. Unsupervised hierarchical clustering analysis was conducted to demonstrate the correlation of expression profiles between treatment and biological replicates.

Journal: Journal of Pain Research

Article Title: Long Non-Coding RNA and mRNA Profiles in the Spinal Cord of Rats with Resiniferatoxin-Induced Neuropathic Pain

doi: 10.2147/JPR.S368599

Figure Lengend Snippet: The expression profile analysis of the lncRNAs/mRNAs and overview of microarray analysis. The purity and quantity of RNA were evaluated by a K5500 micro-spectrophotometer. RNA purity was acceptable if A260/A230 ≥ 0.5 and A260/A280 ≥ 1.5. RNA integrity was acceptable when RIN value ≥ 7 detected by Agilent 2200 RNA assay. Gel electrophoresis ( A ) was conducted to assess the genomic DNA contamination. Expression signal distribution after every mRNA array dataset was normalized ( B ). The microarray heat map of spinal dorsal horn tissues in the PHN model and analysis of differentially expressed lncRNAs (Vehicle group: A1, A2 and A3; PHN model group: B1, B2 and B3) ( C and D ). Red color represented that the relative expression was high and green color represented that the relative expression was low. For advanced data analysis, all biological replicates were pooled and calculated to identify differentially expressed mRNAs based on the threshold of |Fold change| ≥ 1.5 and P ≤ 0.05. Unsupervised hierarchical clustering analysis was conducted to demonstrate the correlation of expression profiles between treatment and biological replicates.

Article Snippet: The RiboArray microArray covering 29,659 unique rat mRNAs and 6713 unique rat lncRNAs (refseq60) was provided by Ribobio (Ribobio Co. Guangzhou, China) via the Combimatrix platform (Washington-Seattle, USA).

Techniques: Expressing, Microarray, Spectrophotometry, Nucleic Acid Electrophoresis

LncRNA-mRNA interaction network diagram. The red box represents lncRNAs, the blue circle represents predicted mRNAs, and the line represents the relationship between lncRNAs and mRNAs. All LncRNA target genes were obtained by LncRNA target gene prediction. The interaction between lncRNAs and target genes was obtained. LncRNA-mRNA interaction network diagram was drawn. Due to the large number of results of this project, lncRNAs with more than 20 target genes were screened ( A ). A network diagram of the relationships between overlapping genes. The intersection of mRNAs predicted by lncRNAs and differential mRNA results was revealed, and the interaction network diagram between the intersection genes and the corresponding lncRNA was drawn ( B ). An overview of the aberrant lncRNAs by analyzing the microarray data ( C ).

Journal: Journal of Pain Research

Article Title: Long Non-Coding RNA and mRNA Profiles in the Spinal Cord of Rats with Resiniferatoxin-Induced Neuropathic Pain

doi: 10.2147/JPR.S368599

Figure Lengend Snippet: LncRNA-mRNA interaction network diagram. The red box represents lncRNAs, the blue circle represents predicted mRNAs, and the line represents the relationship between lncRNAs and mRNAs. All LncRNA target genes were obtained by LncRNA target gene prediction. The interaction between lncRNAs and target genes was obtained. LncRNA-mRNA interaction network diagram was drawn. Due to the large number of results of this project, lncRNAs with more than 20 target genes were screened ( A ). A network diagram of the relationships between overlapping genes. The intersection of mRNAs predicted by lncRNAs and differential mRNA results was revealed, and the interaction network diagram between the intersection genes and the corresponding lncRNA was drawn ( B ). An overview of the aberrant lncRNAs by analyzing the microarray data ( C ).

Article Snippet: The RiboArray microArray covering 29,659 unique rat mRNAs and 6713 unique rat lncRNAs (refseq60) was provided by Ribobio (Ribobio Co. Guangzhou, China) via the Combimatrix platform (Washington-Seattle, USA).

Techniques: Microarray

lncRNAs regulated by nucleolin in cardiomyocytes. (A) Heatmap profile of lncRNA microarray analysis. Green to red colors indicate low to high transcriptional levels. The lncRNAs differentially expressed between the two groups were identified through paired t-test P ≤ 0.05 and a fold change (FC) ≥ 2.5; n = 3 independent biological samples for each group. (B) The expression of 15 selected lncRNAs in chip test, where 10 differentially expressed up-regulated lncRNAs (up) and 5 differentially expressed down-regulated lncRNAs (down) were selected. (C) The interactions between nucleolin and lncRNAs were confirmed by RIP and identified via qRT-PCR. *, P < 0.05, vs. IgG group, n = 3. pcDNA3.1, the empty vector served as negative control; pcDNA3.1-Nuc, overexpression nucleolin group. (D) Bioinformatics website predicted Fendrr binding elements with nucleolin.

Journal: Redox Report : Communications in Free Radical Research

Article Title: LncRNA Fendrr: involvement in the protective role of nucleolin against H 2 O 2 -induced injury in cardiomyocytes

doi: 10.1080/13510002.2023.2168626

Figure Lengend Snippet: lncRNAs regulated by nucleolin in cardiomyocytes. (A) Heatmap profile of lncRNA microarray analysis. Green to red colors indicate low to high transcriptional levels. The lncRNAs differentially expressed between the two groups were identified through paired t-test P ≤ 0.05 and a fold change (FC) ≥ 2.5; n = 3 independent biological samples for each group. (B) The expression of 15 selected lncRNAs in chip test, where 10 differentially expressed up-regulated lncRNAs (up) and 5 differentially expressed down-regulated lncRNAs (down) were selected. (C) The interactions between nucleolin and lncRNAs were confirmed by RIP and identified via qRT-PCR. *, P < 0.05, vs. IgG group, n = 3. pcDNA3.1, the empty vector served as negative control; pcDNA3.1-Nuc, overexpression nucleolin group. (D) Bioinformatics website predicted Fendrr binding elements with nucleolin.

Article Snippet: Using the Aglient Rat lncRNA microarray V2.0 (Arraystar, Rockville, MD, USA), three sample pairs were prepared for lncRNA microarray analysis in the nucleolin-overexpressing rat cardiomyocyte cell line and control group.

Techniques: Microarray, Expressing, Quantitative RT-PCR, Plasmid Preparation, Negative Control, Over Expression, Binding Assay