two step quantitative reverse transcription pcr kit Search Results


rna extraction kit, reverse transcription quantitative real-time pcr kit  (ELK Biotechnology)
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ELK Biotechnology rna extraction kit, reverse transcription quantitative real-time pcr kit
Rna Extraction Kit, Reverse Transcription Quantitative Real Time Pcr Kit, supplied by ELK Biotechnology, 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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m gene quantitative real-time reverse transcription-polymerase chain reaction (qrt-pcr) kit  (iNtRON Biotechnology)
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iNtRON Biotechnology m gene quantitative real-time reverse transcription-polymerase chain reaction (qrt-pcr) kit
M Gene Quantitative Real Time Reverse Transcription Polymerase Chain Reaction (Qrt Pcr) Kit, supplied by iNtRON Biotechnology, 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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Average 90 stars, based on 1 article reviews
m gene quantitative real-time reverse transcription-polymerase chain reaction (qrt-pcr) kit - by Bioz Stars, 2026-10
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reverse transcription-quantitative (rt-q) pcr kit  (Promega)
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Promega reverse transcription-quantitative (rt-q) pcr kit
Reverse Transcription Quantitative (Rt Q) Pcr Kit, supplied by Promega, 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/two+step+quantitative+reverse+transcription+pcr+kit/reverse+transcription+quantitative++rt+q++pcr+kit/pmc08461625-183-7-15
Average 90 stars, based on 1 article reviews
reverse transcription-quantitative (rt-q) pcr kit - by Bioz Stars, 2026-10
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lncrna quantitative reverse transcription polymerase chain reaction (pcr) starter kit  (Ribobio co)
90
Ribobio co lncrna quantitative reverse transcription polymerase chain reaction (pcr) starter kit
SNHG16 was a potential promotor of human placenta-derived mesenchymal stem cell proliferation ability. A: Cell cycle analysis of human placenta-derived mesenchymal stem cells (hP-MSCs) under hypoxic culture via flow cytometry; B: Western blot analysis of AKT phosphorylation in hP-MSCs exposed to hypoxia; C: Circos plot of the long non-coding RNAs (lncRNAs)-messenger (m)RNA co-expression network. The outermost circle is the autosomal distribution. The second and third circles are the distribution of differentially expressed lncRNAs on chromosomes. The red line represents upregulation, and the green line represents downregulation. Higher bars indicate a greater number of differential genes in the interval. The fourth and fifth circles are the distribution of differentially expressed genes on chromosomes, with the same interpretation as <t>lncRNA;</t> D: Part of lncRNA-mRNA interaction network analysis visualized using the Cytoscape software; E: Part of the association analysis of differentially expressed lncRNAs and <t>transcription</t> factors; F: Effects of hypoxia on the expression of SNHG16 in hP-MSCs by quantitative reverse transcription <t>polymerase</t> chain reaction. Data are presented as means ± standard deviation. b P < 0.01.
Lncrna Quantitative Reverse Transcription Polymerase Chain Reaction (Pcr) Starter 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/two+step+quantitative+reverse+transcription+pcr+kit/lncrna+quantitative+reverse+transcription+polymerase+chain+reaction++pcr++starter+kit/pmc09516465-82-45-55
Average 90 stars, based on 1 article reviews
lncrna quantitative reverse transcription polymerase chain reaction (pcr) starter kit - by Bioz Stars, 2026-10
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abi quantitative pcr instrument and a sybr green reverse transcription-polymerase chain reaction kit  (Beijing CWBio)
90
Beijing CWBio abi quantitative pcr instrument and a sybr green reverse transcription-polymerase chain reaction kit
SNHG16 was a potential promotor of human placenta-derived mesenchymal stem cell proliferation ability. A: Cell cycle analysis of human placenta-derived mesenchymal stem cells (hP-MSCs) under hypoxic culture via flow cytometry; B: Western blot analysis of AKT phosphorylation in hP-MSCs exposed to hypoxia; C: Circos plot of the long non-coding RNAs (lncRNAs)-messenger (m)RNA co-expression network. The outermost circle is the autosomal distribution. The second and third circles are the distribution of differentially expressed lncRNAs on chromosomes. The red line represents upregulation, and the green line represents downregulation. Higher bars indicate a greater number of differential genes in the interval. The fourth and fifth circles are the distribution of differentially expressed genes on chromosomes, with the same interpretation as <t>lncRNA;</t> D: Part of lncRNA-mRNA interaction network analysis visualized using the Cytoscape software; E: Part of the association analysis of differentially expressed lncRNAs and <t>transcription</t> factors; F: Effects of hypoxia on the expression of SNHG16 in hP-MSCs by quantitative reverse transcription <t>polymerase</t> chain reaction. Data are presented as means ± standard deviation. b P < 0.01.
Abi Quantitative Pcr Instrument And A Sybr Green Reverse Transcription Polymerase Chain Reaction Kit, supplied by Beijing CWBio, 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/two+step+quantitative+reverse+transcription+pcr+kit/abi+quantitative+pcr+instrument+and+a+sybr+green+reverse+transcription+polymerase+chain+reaction+kit/pm36336010-74-6-19
Average 90 stars, based on 1 article reviews
abi quantitative pcr instrument and a sybr green reverse transcription-polymerase chain reaction kit - by Bioz Stars, 2026-10
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SNHG16 was a potential promotor of human placenta-derived mesenchymal stem cell proliferation ability. A: Cell cycle analysis of human placenta-derived mesenchymal stem cells (hP-MSCs) under hypoxic culture via flow cytometry; B: Western blot analysis of AKT phosphorylation in hP-MSCs exposed to hypoxia; C: Circos plot of the long non-coding RNAs (lncRNAs)-messenger (m)RNA co-expression network. The outermost circle is the autosomal distribution. The second and third circles are the distribution of differentially expressed lncRNAs on chromosomes. The red line represents upregulation, and the green line represents downregulation. Higher bars indicate a greater number of differential genes in the interval. The fourth and fifth circles are the distribution of differentially expressed genes on chromosomes, with the same interpretation as lncRNA; D: Part of lncRNA-mRNA interaction network analysis visualized using the Cytoscape software; E: Part of the association analysis of differentially expressed lncRNAs and transcription factors; F: Effects of hypoxia on the expression of SNHG16 in hP-MSCs by quantitative reverse transcription polymerase chain reaction. Data are presented as means ± standard deviation. b P < 0.01.

Journal: World Journal of Stem Cells

Article Title: Long non-coding RNA SNHG16 promotes human placenta-derived mesenchymal stem cell proliferation capacity through the PI3K/AKT pathway under hypoxia

doi: 10.4252/wjsc.v14.i9.714

Figure Lengend Snippet: SNHG16 was a potential promotor of human placenta-derived mesenchymal stem cell proliferation ability. A: Cell cycle analysis of human placenta-derived mesenchymal stem cells (hP-MSCs) under hypoxic culture via flow cytometry; B: Western blot analysis of AKT phosphorylation in hP-MSCs exposed to hypoxia; C: Circos plot of the long non-coding RNAs (lncRNAs)-messenger (m)RNA co-expression network. The outermost circle is the autosomal distribution. The second and third circles are the distribution of differentially expressed lncRNAs on chromosomes. The red line represents upregulation, and the green line represents downregulation. Higher bars indicate a greater number of differential genes in the interval. The fourth and fifth circles are the distribution of differentially expressed genes on chromosomes, with the same interpretation as lncRNA; D: Part of lncRNA-mRNA interaction network analysis visualized using the Cytoscape software; E: Part of the association analysis of differentially expressed lncRNAs and transcription factors; F: Effects of hypoxia on the expression of SNHG16 in hP-MSCs by quantitative reverse transcription polymerase chain reaction. Data are presented as means ± standard deviation. b P < 0.01.

Article Snippet: Total RNA of cells was obtained using Trizol reagent (Invitrogen, Carlsbad, CA, United States) following the manufacturer’s protocol; the concentration of total RNA was quantified using a NanoDrop-2000 (Thermo Fisher Scientific, Waltham, MA, United States). cDNA was synthesized by reverse transcription reaction using a commercial lncRNA quantitative reverse transcription polymerase chain reaction (PCR) Starter Kit (RiboBio, Guangzhou, China).

Techniques: Derivative Assay, Cell Cycle Assay, Flow Cytometry, Western Blot, Phospho-proteomics, Expressing, Software, Reverse Transcription, Polymerase Chain Reaction, Standard Deviation

Knockdown of SNHG16 attenuated the proliferation ability of human placenta-derived mesenchymal stem cells. A: Quantitative reverse transcription polymerase chain reaction analysis of relative SNHG16 expression after transfection of SNHG16 short hairpin RNA (sh- SNHG16 ) and the corresponding controls (sh-NC) in human placenta-derived mesenchymal stem cells; B: Cell proliferation capacity evaluated by cell counting kit-8 assay; C: Cell cycle measured by flow cytometry; D: The G1 to S phase transition-related proteins and p-AKT detected by western blot analysis. Data are presented as means ± standard deviation. b P < 0.01.

Journal: World Journal of Stem Cells

Article Title: Long non-coding RNA SNHG16 promotes human placenta-derived mesenchymal stem cell proliferation capacity through the PI3K/AKT pathway under hypoxia

doi: 10.4252/wjsc.v14.i9.714

Figure Lengend Snippet: Knockdown of SNHG16 attenuated the proliferation ability of human placenta-derived mesenchymal stem cells. A: Quantitative reverse transcription polymerase chain reaction analysis of relative SNHG16 expression after transfection of SNHG16 short hairpin RNA (sh- SNHG16 ) and the corresponding controls (sh-NC) in human placenta-derived mesenchymal stem cells; B: Cell proliferation capacity evaluated by cell counting kit-8 assay; C: Cell cycle measured by flow cytometry; D: The G1 to S phase transition-related proteins and p-AKT detected by western blot analysis. Data are presented as means ± standard deviation. b P < 0.01.

Article Snippet: Total RNA of cells was obtained using Trizol reagent (Invitrogen, Carlsbad, CA, United States) following the manufacturer’s protocol; the concentration of total RNA was quantified using a NanoDrop-2000 (Thermo Fisher Scientific, Waltham, MA, United States). cDNA was synthesized by reverse transcription reaction using a commercial lncRNA quantitative reverse transcription polymerase chain reaction (PCR) Starter Kit (RiboBio, Guangzhou, China).

Techniques: Knockdown, Derivative Assay, Reverse Transcription, Polymerase Chain Reaction, Expressing, Transfection, shRNA, Cell Counting, Flow Cytometry, Sublimation, Western Blot, Standard Deviation

SNHG16 overexpression resulted in activation of the PI3K/AKT pathway and a significant enhancement in the proliferative rate of human placenta-derived mesenchymal stem cells. A: Quantitative reverse transcription polymerase chain reaction analysis of relative SNHG16 expression after transfection of lentivirus overexpressing SNHG16 ( SNHG16 -OE) and the corresponding empty vector in human placenta-derived mesenchymal stem cells; B: Cell proliferation after SNHG16 overexpression was evaluated by cell counting kit-8 assay; C: Cell cycle distribution after SNHG16 overexpression was evaluated by flow cytometry; D: The expression levels of CDK2, CDK4, CDK6, cyclin E1, cyclin D1, and phosphorylated AKT. Data are presented as the means ± SD obtained from three separate experiments. b P < 0.01.

Journal: World Journal of Stem Cells

Article Title: Long non-coding RNA SNHG16 promotes human placenta-derived mesenchymal stem cell proliferation capacity through the PI3K/AKT pathway under hypoxia

doi: 10.4252/wjsc.v14.i9.714

Figure Lengend Snippet: SNHG16 overexpression resulted in activation of the PI3K/AKT pathway and a significant enhancement in the proliferative rate of human placenta-derived mesenchymal stem cells. A: Quantitative reverse transcription polymerase chain reaction analysis of relative SNHG16 expression after transfection of lentivirus overexpressing SNHG16 ( SNHG16 -OE) and the corresponding empty vector in human placenta-derived mesenchymal stem cells; B: Cell proliferation after SNHG16 overexpression was evaluated by cell counting kit-8 assay; C: Cell cycle distribution after SNHG16 overexpression was evaluated by flow cytometry; D: The expression levels of CDK2, CDK4, CDK6, cyclin E1, cyclin D1, and phosphorylated AKT. Data are presented as the means ± SD obtained from three separate experiments. b P < 0.01.

Article Snippet: Total RNA of cells was obtained using Trizol reagent (Invitrogen, Carlsbad, CA, United States) following the manufacturer’s protocol; the concentration of total RNA was quantified using a NanoDrop-2000 (Thermo Fisher Scientific, Waltham, MA, United States). cDNA was synthesized by reverse transcription reaction using a commercial lncRNA quantitative reverse transcription polymerase chain reaction (PCR) Starter Kit (RiboBio, Guangzhou, China).

Techniques: Over Expression, Activation Assay, Derivative Assay, Reverse Transcription, Polymerase Chain Reaction, Expressing, Transfection, Plasmid Preparation, Cell Counting, Flow Cytometry