ncode mirna labelling system Search Results


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Thermo Fisher qrt pcr kits
Sequences of primers used in this study for <t> qRT-PCR. </t>
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Genisphere llc ncode mirna microarray controls
Sequences of primers used in this study for <t> qRT-PCR. </t>
Ncode Mirna Microarray Controls, supplied by Genisphere llc, 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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Thermo Fisher ncode vilo mirna complementary dna synthesis kit
Sequences of primers used in this study for <t> qRT-PCR. </t>
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Thermo Fisher ncode™ sybr® green mirna q pcr kit
Sequences of primers used in this study for <t> qRT-PCR. </t>
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Thermo Fisher ncode™ sybr ® green mirna quantitative real-time pcr (qrtpcr) kit
Sequences of primers used in this study for <t> qRT-PCR. </t>
Ncode™ Sybr ® Green Mirna Quantitative Real Time Pcr (Qrtpcr) Kit, supplied by Thermo Fisher, 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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Ribobio co ncode mirna qrt-pcr analysis
Sequences of primers used in this study for <t> qRT-PCR. </t>
Ncode Mirna Qrt Pcr Analysis, 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
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Image Search Results


Sequences of primers used in this study for  qRT-PCR.

Journal: PLoS ONE

Article Title: Identification and Comparative Analysis of the Tegillarca granosa Haemocytes MicroRNA Transcriptome in Response to Cd Using a Deep Sequencing Approach

doi: 10.1371/journal.pone.0093619

Figure Lengend Snippet: Sequences of primers used in this study for qRT-PCR.

Article Snippet: NCode miRNA First-Strand cDNA Synthesis and qRT-PCR Kits (Ambion, USA) was used for polyadenylation and reverse transcription of miRNAs for use in two-step quantitative RT-PCR.

Techniques:

A. Fold change of five miRNAs that were differentially expressed between C and E library based on deep sequencing data. B. The relative expression abundance of the five miRNAs in haemocytes at challenge with the gradient concentration of 25, 250 and 500 μg/L Cd 2+ by qRT-PCR. * P <0.05, ** P <0.01. The amount relative to the internal control U6 is expressed as mean ± SD (N = 3).

Journal: PLoS ONE

Article Title: Identification and Comparative Analysis of the Tegillarca granosa Haemocytes MicroRNA Transcriptome in Response to Cd Using a Deep Sequencing Approach

doi: 10.1371/journal.pone.0093619

Figure Lengend Snippet: A. Fold change of five miRNAs that were differentially expressed between C and E library based on deep sequencing data. B. The relative expression abundance of the five miRNAs in haemocytes at challenge with the gradient concentration of 25, 250 and 500 μg/L Cd 2+ by qRT-PCR. * P <0.05, ** P <0.01. The amount relative to the internal control U6 is expressed as mean ± SD (N = 3).

Article Snippet: NCode miRNA First-Strand cDNA Synthesis and qRT-PCR Kits (Ambion, USA) was used for polyadenylation and reverse transcription of miRNAs for use in two-step quantitative RT-PCR.

Techniques: Sequencing, Expressing, Concentration Assay, Quantitative RT-PCR