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superscript iii first-strand synthesis system 18080051  (Thermo Fisher)


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    Structured Review

    Thermo Fisher superscript iii first-strand synthesis system 18080051
    Superscript Iii First Strand Synthesis System 18080051, 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
    https://www.bioz.com/product/superscript+iii+first-strand+synthesis+system+18080051/high+capacity+cdna+reverse+transcription+kit/bio_rxiv__2025__07__15__664932-209-18-24
    Average 90 stars, based on 1 article reviews
    superscript iii first-strand synthesis system 18080051 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Reverse Transcription:

    Article Title: Neuronal substance-P drives breast cancer growth and metastasis via an extracellular RNA-TLR7 axis
    Article Snippet: RNA was extracted from cells using the RNA purification kit (Norgen Biotek, 37500)), according to the manufacturer’s protocol. .. Reverse transcription (RT-PCR) was performed on 2-5 μg of RNA using the SuperScript III First-Strand Synthesis System (ThermoFisher Scientific, 18080051). .. Real time qPCR was conducted in a 384-well PCR microplate (Fisher scientific, AB-1384) performed on an Applied Biosystem StepOne Real-Time PCR System using the Fast SYBR Green master mix (Fisher Scientific, 43-856-18).

    Article Title: Neuronal substance-P drives metastasis via an extracellular RNA/TLR7 axis
    Article Snippet: RNA was extracted from cells using the RNA purification kit (Norgen Biotek, 37500), according to the manufacturer’s protocol. .. Reverse transcription (RT-PCR) was performed on 2–5 μg of RNA using the SuperScript III First-Strand Synthesis System (ThermoFisher Scientific, 18080051). .. Real time qPCR was conducted in a 384-well PCR microplate (Fisher scientific, AB-1384) performed on an Applied Biosystem StepOne Real-Time PCR System using Fast SYBR Green master mix (Fisher Scientific, 43-856-18).

    Article Title: A double-agent microRNA regulates viral cross-kingdom infection in animals and plants
    Article Snippet: RNA quality was detected by a NanoDrop One (Thermo Scientific, Waltham, MA; 840-317400) and gel electrophoresis. .. For mRNA or viral RNA qPCR, 2 μg of RNA was reverse transcribed to cDNA by using the Superscript III First-Strand Synthesis System (Thermo Scientific; 18080051) and random primers (Promega, Madison, WI; C1181) (Zhao et al, ). .. For miRNA qPCR, 2 μg of RNA was reverse transcribed by using miRNA RT enzyme mix of a miRcute plus miRNA first-strand cDNA kit (Tiangen, Beijing, China; KR211) (Zhao et al, ). qPCR amplification was performed on a LightCycler® 480 instrument II (Roche, Basel, Switzerland) using a LightCycler® 480 SYBR Green I Master (Roche; 04887352001), or a miRcute miRNA qPCR Detection Kit (Tiangen; FP411), respectively.

    Article Title: Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development
    Article Snippet: For qRT-PCR expression assays, at least three independent RNA samples per developmental stage were extracted from whole embryos (10–12 pooled embryos per sample), dissected embryonic eyes (30–40 pooled eyes per sample) and midbrains (20–25 pooled brains per sample) using Direct-zol RNA MiniPrep kit (Zymo Research, cat#R2052). .. To remove DNA contamination, 1 μg of RNA was digested with 1 unit of DNaseI (ThermoFisher, cat# EN0523) for 15 min at room temperature (RT) and inactivated in the presence of 2.5 mM EDTA for 10 min at 65 ◦ C. Reverse transcription was performed using the SuperScript III First-Strand Synthesis System (ThermoFisher, cat# 18080051). .. Quantitative RT-PCR was performed using SYBR Green PCR Master Mix (Applied Biosystems, Waltham, MA, cat# 43-676-59) and CFX384 Touch Real-Time PCR Detection Systems (Bio-Rad, Hercules, CA).

    Article Title: Bidirectional control of a metabolic transition by the GID ubiquitin ligase
    Article Snippet: .. Contaminating genomic DNA was removed using the RNase-Free DNase Set (79254, Qiagen), followed by reverse transcription with the SuperScript III First-Strand Synthesis System (18080051, Thermo Fisher Scientific) according to manufacturer’s instructions. .. Quantitative PCR was performed using the PowerUp SYBR Green Master Mix (A25780, Thermo Fisher Scientific) and primers Gid11_F/R (primers #1 and #2 in Supplementary Table 3) for detecting the GID11 mRNA or primers Alg9_F/R (primers #3 and #4 in Supplementary Table 3) for detecting the ALG9 mRNA as a stable reference ( ).

    other:

    Article Title: A commonly inherited human PCSK9 germline variant drives breast cancer metastasis via LRP1 receptor.
    Article Snippet: Article A commonly inherited human PCSK9 germline variant drives breast cancer metastasis via LRP1 receptor

    Polymerase Chain Reaction:

    Article Title: The contribution of de novo coding mutations to meningomyelocele.
    Article Snippet: RNA was extracted from patient and control fibroblast cells using TRIzol reagent (ThermoFisher Scientific, 15596026) following the manufacturer’s guidelines. .. The extracted RNA was used to synthesize cDNA using the SuperScript III First-Strand Synthesis System (ThermoFisher Scientific, 18080051) and the provided Oligo(dT)20 primer set. cDNA (30 ng) was used to perform PCR with the following DNAH5 primers using GoTaq Green Master Mix (Promega, M7122). ..

    Real-time Polymerase Chain Reaction:

    Article Title: A double-agent microRNA regulates viral cross-kingdom infection in animals and plants
    Article Snippet: RNA quality was detected by a NanoDrop One (Thermo Scientific, Waltham, MA; 840-317400) and gel electrophoresis. .. For mRNA or viral RNA qPCR, 2 μg of RNA was reverse transcribed to cDNA by using the Superscript III First-Strand Synthesis System (Thermo Scientific; 18080051) and random primers (Promega, Madison, WI; C1181) (Zhao et al, ). .. For miRNA qPCR, 2 μg of RNA was reverse transcribed by using miRNA RT enzyme mix of a miRcute plus miRNA first-strand cDNA kit (Tiangen, Beijing, China; KR211) (Zhao et al, ). qPCR amplification was performed on a LightCycler® 480 instrument II (Roche, Basel, Switzerland) using a LightCycler® 480 SYBR Green I Master (Roche; 04887352001), or a miRcute miRNA qPCR Detection Kit (Tiangen; FP411), respectively.

    Incubation:

    Article Title: Discovery of the first-in-class DOT1L PROTAC degrader.
    Article Snippet: DOT1L is the lysine methyltransferase responsible for histone H3 lysine 79 (H3K79) methylation and plays a crucial role in leukemia progression.. Furthermore, DOT1L has biological functions that are independent of its methyltransferase activity.. Therefore, targeting and degrading DOT1L with PROteolysis TArgeting Chimeras (PROTACs) could represent a promising therapeutic strategy.

    cDNA Synthesis:

    Article Title: Discovery of the first-in-class DOT1L PROTAC degrader.
    Article Snippet: DOT1L is the lysine methyltransferase responsible for histone H3 lysine 79 (H3K79) methylation and plays a crucial role in leukemia progression.. Furthermore, DOT1L has biological functions that are independent of its methyltransferase activity.. Therefore, targeting and degrading DOT1L with PROteolysis TArgeting Chimeras (PROTACs) could represent a promising therapeutic strategy.



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