in solution hybridization kit Search Results


standard amine reactive antibody labeling kits invitrogen n a citrate buffer antigen retrieval solution  (Thermo Fisher)
99
Thermo Fisher standard amine reactive antibody labeling kits invitrogen n a citrate buffer antigen retrieval solution
Standard Amine Reactive Antibody Labeling Kits Invitrogen N A Citrate Buffer Antigen Retrieval Solution, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/Citrate+Buffer/pm40652508-114-198-204
Average 99 stars, based on 1 article reviews
standard amine reactive antibody labeling kits invitrogen n a citrate buffer antigen retrieval solution - by Bioz Stars, 2026-09
99/100 stars
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nebnext rrna depletion solution bacteria  (New England Biolabs)
99
New England Biolabs nebnext rrna depletion solution bacteria
Nebnext Rrna Depletion Solution Bacteria, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/NEBNext+rRNA+Depletion+Kit/pm35950875-325-5-5
Average 99 stars, based on 1 article reviews
nebnext rrna depletion solution bacteria - by Bioz Stars, 2026-09
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peripheral blood mononuclear cells pbmcs  (Beijing Solarbio Science)
93
Beijing Solarbio Science peripheral blood mononuclear cells pbmcs
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
Peripheral Blood Mononuclear Cells Pbmcs, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/Fish+Peripheral+Blood+Mononuclear+Cell+Separation+Solution+Kit/pmc09729135-28-0-11
Average 93 stars, based on 1 article reviews
peripheral blood mononuclear cells pbmcs - by Bioz Stars, 2026-09
93/100 stars
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rapid capture exome enrichment kit  (Illumina Inc)
95
Illumina Inc rapid capture exome enrichment kit
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
Rapid Capture Exome Enrichment Kit, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/Nextera+Rapid+Capture+Custom+Enrichment+Kit/pmc08059372-97-9-8
Average 95 stars, based on 1 article reviews
rapid capture exome enrichment kit - by Bioz Stars, 2026-09
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pre hybridization solution  (Thermo Fisher)
99
Thermo Fisher pre hybridization solution
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
Pre Hybridization Solution, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/SODIUM+DODECYLSULFATE+SOLUTION/pm12751315-84-9-36
Average 99 stars, based on 1 article reviews
pre hybridization solution - by Bioz Stars, 2026-09
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nebnext rrna depletion solution  (New England Biolabs)
99
New England Biolabs nebnext rrna depletion solution
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
Nebnext Rrna Depletion Solution, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/NEBNext+rRNA+Depletion+Kit+v2/pmc12435222-145-6-6
Average 99 stars, based on 1 article reviews
nebnext rrna depletion solution - by Bioz Stars, 2026-09
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xgen lockdown reagents kit  (Integrated DNA Technologies)
95
Integrated DNA Technologies xgen lockdown reagents kit
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
Xgen Lockdown Reagents Kit, supplied by Integrated DNA Technologies, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/xGen+Hybridization+and+Wash+Kit/pmc07393544-90-16-23
Average 95 stars, based on 1 article reviews
xgen lockdown reagents kit - by Bioz Stars, 2026-09
95/100 stars
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truseqtm  (Illumina Inc)
99
Illumina Inc truseqtm
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
Truseqtm, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/TruSeq+Exome+Kit/pm24102379-58-15-16
Average 99 stars, based on 1 article reviews
truseqtm - by Bioz Stars, 2026-09
99/100 stars
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™ fluorescent situ hybridization kit  (Ribobio co)
90
Ribobio co ™ fluorescent situ hybridization kit
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
™ Fluorescent Situ Hybridization Kit, 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/product/in+solution+hybridization+kit/fluorescent+in+situ+hybridization+kit/pmc06099154-54-13-18
Average 90 stars, based on 1 article reviews
™ fluorescent situ hybridization kit - by Bioz Stars, 2026-09
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nebnext rrna depletion solution human mouse rat  (New England Biolabs)
97
New England Biolabs nebnext rrna depletion solution human mouse rat
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
Nebnext Rrna Depletion Solution Human Mouse Rat, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/in+solution+hybridization+kit/NEBNext+rRNA+Depletion+Kit/bio_rxiv__2022__01__05__475126-274-6-6
Average 97 stars, based on 1 article reviews
nebnext rrna depletion solution human mouse rat - by Bioz Stars, 2026-09
97/100 stars
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her-2/csp17dna probe kit  (Beijing GP Medical Technologies)
90
Beijing GP Medical Technologies her-2/csp17dna probe kit
Secondary sequencing uncovered CHD-related <t>PBMC</t> circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD
Her 2/Csp17dna Probe Kit, supplied by Beijing GP Medical Technologies, 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/product/in+solution+hybridization+kit/her2+probe/pm24592124-22-1-26
Average 90 stars, based on 1 article reviews
her-2/csp17dna probe kit - by Bioz Stars, 2026-09
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Image Search Results


Secondary sequencing uncovered CHD-related PBMC circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD

Journal: Cellular and Molecular Life Sciences

Article Title: Role of hsa_circ_0000280 in regulating vascular smooth muscle cell function and attenuating neointimal hyperplasia via ELAVL1

doi: 10.1007/s00018-022-04602-w

Figure Lengend Snippet: Secondary sequencing uncovered CHD-related PBMC circRNAs, validated by qRT-PCR in human atherosclerotic vessels. A Volcano plot of sequenced PBMC circRNAs. X-axis, fold modification expressed as log2; Y-axis: p value expressed as − log10. Horizontal line represents p = 0.05. Compared with the control, red and green points exhibited significantly upregulated and downregulated circRNAs at p < 0.05 and p < 0.05, respectively. Blue point represents hsa_circ_0000280 (CHD, n = 70; control, n = 30; Student t test). B ELAVL1 RIP-sequencing revealed top seven circRNAs. C Abundance of top seven circRNAs in three types of cardiovascular cells ( n = 3). D Expression of three circRNAs measured in PDGF-BB-induced HASMCs ( n = 3, p < 0.01; Student t tests). E Quantitative RT-PCR analysis of hsa_circ_0000280 in human coronary arteries with and without (matched controls) luminal stenosis. ( n = 5 pairs, p = 0.005; Student t test). F , G Fluorescence in situ hybridization assay (FISH) shows location and expression of hsa_circ_0000280 in control and CHD tissues. White arrows indicate intimal layer. Probes for hsa_circ_0000280 were labeled with Cy3. Scale bar, 100 µm ( n = 5 pairs, p = 0.0038; Student t tests). Data are presented as means ± SD

Article Snippet: Peripheral blood mononuclear cells (PBMCs) were processed, dispersed using separation medium (Solarbio, Beijing, China) and centrifuged twice at 2,000 rpm for 40 min.

Techniques: Sequencing, Quantitative RT-PCR, Modification, Control, Expressing, Fluorescence, In Situ Hybridization, Labeling