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random hexanucleotide primers  (Millipore)


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    Structured Review

    Millipore random hexanucleotide primers
    Random Hexanucleotide Primers, supplied by Millipore, 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/random+primer+hexanucleotides/random+hexamer+primers/pm37371461-64-43-46
    Average 90 stars, based on 1 article reviews
    random hexanucleotide primers - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Extraction:

    Article Title: Nucleolar Localization of the RNA Helicase DDX21 Predicts Survival Outcomes in Gynecologic Cancers
    Article Snippet: The membranes were washed extensively with TBS-T before chemiluminescent detection using SuperSignal West Pico substrate (Thermo Fisher Scientific) and ChemiDoc system (Bio-Rad). .. cDNA pools were prepared by extraction of nuclear RNA from cells treated with niraparib using the Qiagen RNeasy Plus Mini Kit, followed by reverse transcription using MMLV reverse transcriptase (Progmega, M150B) with random hexamer primers (Sigma-Aldrich) to generate a cDNA pool. .. The cDNA was analyzed by qPCR using the primer sets listed below and a LightCycler 480 real-time PCR thermocycler (Roche) for 45 cycles.

    Reverse Transcription:

    Article Title: Nucleolar Localization of the RNA Helicase DDX21 Predicts Survival Outcomes in Gynecologic Cancers
    Article Snippet: The membranes were washed extensively with TBS-T before chemiluminescent detection using SuperSignal West Pico substrate (Thermo Fisher Scientific) and ChemiDoc system (Bio-Rad). .. cDNA pools were prepared by extraction of nuclear RNA from cells treated with niraparib using the Qiagen RNeasy Plus Mini Kit, followed by reverse transcription using MMLV reverse transcriptase (Progmega, M150B) with random hexamer primers (Sigma-Aldrich) to generate a cDNA pool. .. The cDNA was analyzed by qPCR using the primer sets listed below and a LightCycler 480 real-time PCR thermocycler (Roche) for 45 cycles.

    Article Title: Systematic surveillance of SARS-CoV-2 reveals dynamics of variant mutagenesis and transmission in a large urban population
    Article Snippet: .. Total RNA was reverse transcribed using SuperScriptTM IV Reverse Transcriptase (Invitrogen) in 5X First-Strand Buffer containing DTT, a custom mix of Oligo-dT (Sigma), and Hexamer random primers (Sigma), dNTPs (Genedirex). ..

    Article Title: A noncanonical repressor function of JUN restrains YAP activity and suppresses YAP-dependent liver cancer growth
    Article Snippet: Total RNA was extracted with peqGOLD TriFast Reagent (VWR). .. First-strand cDNA synthesis was performed from 1 μg RNA using M-MLV Reverse Transcriptase (Promega) and random hexamer primers (Sigma-Aldrich) following the manufactureŕs instructions. qPCR reactions were conducted in technical triplicates using InnuMIX qPCR DSGreen Standard Mix (Analytik Jena) on a StepOnePlusTM Real-Time PCR System (Thermo Fisher Scientific). ..

    Article Title: HIV-1 Transcriptional Activator Tat Inhibits IL2 Expression by Preventing the Presence of Pol II on the IL2 Promoter.
    Article Snippet: RNA yield and purity were determined by measuring absorbance at 260/280 nm on a Quawell microvolume spectrophotometer Q3000 (Quawell Technology). .. Total RNA (100 ng per reaction) was used for cDNA synthesis using M-MLV reverse transcriptase (200 U/μL) (Sigma-Aldrich, St. Louis, MI, USA) in 10× M-MLV reverse transcriptase buffer, 40 U/μL RNase inhibitor (Thermo Fisher Scientific-Invitrogen), 1 mM each dNTPs (Sigma-Aldrich), and 2.5 μM random hexanucleotide primers (SigmaAldrich). qPCR mRNA analysis was performed on an Mx3000PTM Quantitative PCR System Thermocycler (Stratagene, San Diego, MA, USA) using SYBR-green fluorescence quantification technology (KAPA SYBR FAST qPCR Kit, Kapa Biosystems, Wilmington, MA, USA). ..

    Article Title: Genome-wide analysis of growth phase-dependent translational and transcriptional regulation in halophilic archaea
    Article Snippet: .. Reverse transcription of 2 μg RNA was carried out with 400 U M-MLV reverse transcriptase RNase H minus (Promega, Mannheim, Germany) and 0.6 μg random hexamer primers (Sigma, Steinheim, Germany) in 40 μl 1× reaction buffer (Promega) in the presence of 0.2 mM dATP and dTTP as well as 0.3 mM dCTP and dGTP. ..

    Article Title: Gypenoside A Protects Human Myocardial Cells from Ischemia/Reperfusion Injury via the circ_0010729/miR-370-3p/RUNX1 Axis
    Article Snippet: Ischemia/reperfusion (I/R) injury is one of the major causes of cardiovascular disease.. Gypenoside A (GP), the main active component of Gynostemma pentaphyllum, alleviates myocardial I/R injury.. Circular RNAs (circRNAs) and microRNAs (miRNAs) are involved in the I/R injury.

    Random Hexamer:

    Article Title: Nucleolar Localization of the RNA Helicase DDX21 Predicts Survival Outcomes in Gynecologic Cancers
    Article Snippet: The membranes were washed extensively with TBS-T before chemiluminescent detection using SuperSignal West Pico substrate (Thermo Fisher Scientific) and ChemiDoc system (Bio-Rad). .. cDNA pools were prepared by extraction of nuclear RNA from cells treated with niraparib using the Qiagen RNeasy Plus Mini Kit, followed by reverse transcription using MMLV reverse transcriptase (Progmega, M150B) with random hexamer primers (Sigma-Aldrich) to generate a cDNA pool. .. The cDNA was analyzed by qPCR using the primer sets listed below and a LightCycler 480 real-time PCR thermocycler (Roche) for 45 cycles.

    Article Title: Prevalence of HSPB6 gene variants in peripartum cardiomyopathy: Data from the German PPCM registry.
    Article Snippet: The in silico splicing tools SSF, MaxEntScan and NNSPLICE (integrated part of Alamut v2.11.0, Interactive Biosoftware, Rouen, France) were used for splicing prediction. .. Total RNA from myocardial biopsies were isolated with TRIzol® Reagent (Life technologies) in accordance with the manufacturer’s instructions. cDNA synthesis using Superscript III (Invitrogen), 2 μg of total RNA and random hexamer primers (SIGMA-Aldrich) was performed according to the manufacturer’s protocols as previously described [17]. .. Semi-quantitative real-time PCR using the SYBR green dye method (SYBR Green qPCR 2xMastermix-Kit, Thermo Fisher Scientific) was performed with the AriaMX Real-Time PCR System (Agilent Technologies). mRNA expression levels were normalised using the 2- ΔΔCT method relative to 18S.

    Article Title: A noncanonical repressor function of JUN restrains YAP activity and suppresses YAP-dependent liver cancer growth
    Article Snippet: Total RNA was extracted with peqGOLD TriFast Reagent (VWR). .. First-strand cDNA synthesis was performed from 1 μg RNA using M-MLV Reverse Transcriptase (Promega) and random hexamer primers (Sigma-Aldrich) following the manufactureŕs instructions. qPCR reactions were conducted in technical triplicates using InnuMIX qPCR DSGreen Standard Mix (Analytik Jena) on a StepOnePlusTM Real-Time PCR System (Thermo Fisher Scientific). ..

    Article Title: Genome-wide analysis of growth phase-dependent translational and transcriptional regulation in halophilic archaea
    Article Snippet: .. Reverse transcription of 2 μg RNA was carried out with 400 U M-MLV reverse transcriptase RNase H minus (Promega, Mannheim, Germany) and 0.6 μg random hexamer primers (Sigma, Steinheim, Germany) in 40 μl 1× reaction buffer (Promega) in the presence of 0.2 mM dATP and dTTP as well as 0.3 mM dCTP and dGTP. ..

    Article Title: Gypenoside A Protects Human Myocardial Cells from Ischemia/Reperfusion Injury via the circ_0010729/miR-370-3p/RUNX1 Axis
    Article Snippet: Ischemia/reperfusion (I/R) injury is one of the major causes of cardiovascular disease.. Gypenoside A (GP), the main active component of Gynostemma pentaphyllum, alleviates myocardial I/R injury.. Circular RNAs (circRNAs) and microRNAs (miRNAs) are involved in the I/R injury.

    Isolation:

    Article Title: Prevalence of HSPB6 gene variants in peripartum cardiomyopathy: Data from the German PPCM registry.
    Article Snippet: The in silico splicing tools SSF, MaxEntScan and NNSPLICE (integrated part of Alamut v2.11.0, Interactive Biosoftware, Rouen, France) were used for splicing prediction. .. Total RNA from myocardial biopsies were isolated with TRIzol® Reagent (Life technologies) in accordance with the manufacturer’s instructions. cDNA synthesis using Superscript III (Invitrogen), 2 μg of total RNA and random hexamer primers (SIGMA-Aldrich) was performed according to the manufacturer’s protocols as previously described [17]. .. Semi-quantitative real-time PCR using the SYBR green dye method (SYBR Green qPCR 2xMastermix-Kit, Thermo Fisher Scientific) was performed with the AriaMX Real-Time PCR System (Agilent Technologies). mRNA expression levels were normalised using the 2- ΔΔCT method relative to 18S.

    cDNA Synthesis:

    Article Title: Prevalence of HSPB6 gene variants in peripartum cardiomyopathy: Data from the German PPCM registry.
    Article Snippet: The in silico splicing tools SSF, MaxEntScan and NNSPLICE (integrated part of Alamut v2.11.0, Interactive Biosoftware, Rouen, France) were used for splicing prediction. .. Total RNA from myocardial biopsies were isolated with TRIzol® Reagent (Life technologies) in accordance with the manufacturer’s instructions. cDNA synthesis using Superscript III (Invitrogen), 2 μg of total RNA and random hexamer primers (SIGMA-Aldrich) was performed according to the manufacturer’s protocols as previously described [17]. .. Semi-quantitative real-time PCR using the SYBR green dye method (SYBR Green qPCR 2xMastermix-Kit, Thermo Fisher Scientific) was performed with the AriaMX Real-Time PCR System (Agilent Technologies). mRNA expression levels were normalised using the 2- ΔΔCT method relative to 18S.

    Article Title: A noncanonical repressor function of JUN restrains YAP activity and suppresses YAP-dependent liver cancer growth
    Article Snippet: Total RNA was extracted with peqGOLD TriFast Reagent (VWR). .. First-strand cDNA synthesis was performed from 1 μg RNA using M-MLV Reverse Transcriptase (Promega) and random hexamer primers (Sigma-Aldrich) following the manufactureŕs instructions. qPCR reactions were conducted in technical triplicates using InnuMIX qPCR DSGreen Standard Mix (Analytik Jena) on a StepOnePlusTM Real-Time PCR System (Thermo Fisher Scientific). ..

    Article Title: HIV-1 Transcriptional Activator Tat Inhibits IL2 Expression by Preventing the Presence of Pol II on the IL2 Promoter.
    Article Snippet: RNA yield and purity were determined by measuring absorbance at 260/280 nm on a Quawell microvolume spectrophotometer Q3000 (Quawell Technology). .. Total RNA (100 ng per reaction) was used for cDNA synthesis using M-MLV reverse transcriptase (200 U/μL) (Sigma-Aldrich, St. Louis, MI, USA) in 10× M-MLV reverse transcriptase buffer, 40 U/μL RNase inhibitor (Thermo Fisher Scientific-Invitrogen), 1 mM each dNTPs (Sigma-Aldrich), and 2.5 μM random hexanucleotide primers (SigmaAldrich). qPCR mRNA analysis was performed on an Mx3000PTM Quantitative PCR System Thermocycler (Stratagene, San Diego, MA, USA) using SYBR-green fluorescence quantification technology (KAPA SYBR FAST qPCR Kit, Kapa Biosystems, Wilmington, MA, USA). ..

    Real-time Polymerase Chain Reaction:

    Article Title: A noncanonical repressor function of JUN restrains YAP activity and suppresses YAP-dependent liver cancer growth
    Article Snippet: Total RNA was extracted with peqGOLD TriFast Reagent (VWR). .. First-strand cDNA synthesis was performed from 1 μg RNA using M-MLV Reverse Transcriptase (Promega) and random hexamer primers (Sigma-Aldrich) following the manufactureŕs instructions. qPCR reactions were conducted in technical triplicates using InnuMIX qPCR DSGreen Standard Mix (Analytik Jena) on a StepOnePlusTM Real-Time PCR System (Thermo Fisher Scientific). ..

    Article Title: Unique features of KGN granulosa-like tumour cells in the regulation of steroidogenic and antioxidant genes.
    Article Snippet: DNaseI (Promega/Life Technologies Australia Pty Ltd, Tullamarine, Vic, Australia) was also employed to eliminate the potential genomic DNA contamination of the RNA. .. One hundred ng of high-quality DNase-treated RNA was used to synthesise cDNA with 250 ng random hexamer primers (Sigma-Aldrich/Merck, St. Louis, MO, USA) and 200 U Superscript III reverse transcriptase (Thermo Fisher Scientific, Waltham, MA, USA), followed by quantitative real time-PCR (qRT-PCR) using Power SYBRTM Green PCR Master Mix (Applied Biosystems, Foster City, CA, USA). ..

    Article Title: HIV-1 Transcriptional Activator Tat Inhibits IL2 Expression by Preventing the Presence of Pol II on the IL2 Promoter.
    Article Snippet: RNA yield and purity were determined by measuring absorbance at 260/280 nm on a Quawell microvolume spectrophotometer Q3000 (Quawell Technology). .. Total RNA (100 ng per reaction) was used for cDNA synthesis using M-MLV reverse transcriptase (200 U/μL) (Sigma-Aldrich, St. Louis, MI, USA) in 10× M-MLV reverse transcriptase buffer, 40 U/μL RNase inhibitor (Thermo Fisher Scientific-Invitrogen), 1 mM each dNTPs (Sigma-Aldrich), and 2.5 μM random hexanucleotide primers (SigmaAldrich). qPCR mRNA analysis was performed on an Mx3000PTM Quantitative PCR System Thermocycler (Stratagene, San Diego, MA, USA) using SYBR-green fluorescence quantification technology (KAPA SYBR FAST qPCR Kit, Kapa Biosystems, Wilmington, MA, USA). ..

    Polymerase Chain Reaction:

    Article Title: Unique features of KGN granulosa-like tumour cells in the regulation of steroidogenic and antioxidant genes.
    Article Snippet: DNaseI (Promega/Life Technologies Australia Pty Ltd, Tullamarine, Vic, Australia) was also employed to eliminate the potential genomic DNA contamination of the RNA. .. One hundred ng of high-quality DNase-treated RNA was used to synthesise cDNA with 250 ng random hexamer primers (Sigma-Aldrich/Merck, St. Louis, MO, USA) and 200 U Superscript III reverse transcriptase (Thermo Fisher Scientific, Waltham, MA, USA), followed by quantitative real time-PCR (qRT-PCR) using Power SYBRTM Green PCR Master Mix (Applied Biosystems, Foster City, CA, USA). ..

    Fluorescence:

    Article Title: HIV-1 Transcriptional Activator Tat Inhibits IL2 Expression by Preventing the Presence of Pol II on the IL2 Promoter.
    Article Snippet: RNA yield and purity were determined by measuring absorbance at 260/280 nm on a Quawell microvolume spectrophotometer Q3000 (Quawell Technology). .. Total RNA (100 ng per reaction) was used for cDNA synthesis using M-MLV reverse transcriptase (200 U/μL) (Sigma-Aldrich, St. Louis, MI, USA) in 10× M-MLV reverse transcriptase buffer, 40 U/μL RNase inhibitor (Thermo Fisher Scientific-Invitrogen), 1 mM each dNTPs (Sigma-Aldrich), and 2.5 μM random hexanucleotide primers (SigmaAldrich). qPCR mRNA analysis was performed on an Mx3000PTM Quantitative PCR System Thermocycler (Stratagene, San Diego, MA, USA) using SYBR-green fluorescence quantification technology (KAPA SYBR FAST qPCR Kit, Kapa Biosystems, Wilmington, MA, USA). ..

    Purification:

    Article Title: Gypenoside A Protects Human Myocardial Cells from Ischemia/Reperfusion Injury via the circ_0010729/miR-370-3p/RUNX1 Axis
    Article Snippet: Ischemia/reperfusion (I/R) injury is one of the major causes of cardiovascular disease.. Gypenoside A (GP), the main active component of Gynostemma pentaphyllum, alleviates myocardial I/R injury.. Circular RNAs (circRNAs) and microRNAs (miRNAs) are involved in the I/R injury.



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