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dtt from superscript tm iv kit  (Thermo Fisher)


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    Structured Review

    Thermo Fisher dtt from superscript tm iv kit
    Dtt From Superscript Tm Iv Kit, 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/superscript+iv/DITHIOTHREITOL/pmc12550521-209-1-7
    Average 99 stars, based on 1 article reviews
    dtt from superscript tm iv kit - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Reverse Transcription:

    Article Title: RtmR is a membrane-embedded RRM-family RNA-binding protein that regulates biofilm formation
    Article Snippet: .. RNAs were then recovered following an overnight sodium acetate precipitation with GlycoBlue (ThermoFisher) and a selected reverse transcription primer, and reverse-transcribed using SuperScript IV (Invitrogen). .. RNAs were then degraded with NaOH treatment followed by neutralization with HCl, and cDNA was purified using Agencourt AMPure XP beads (Beckman Coulter).

    Article Title: Methods of adding polymers to ribonucleic acids
    Article Snippet: 480 μl of the aqueous phase was combined with 1.2 mL of 100% ethanol in a fresh 1.7 mL Eppendorf tube. .. Superscript IV (Thermo Fisher) was used for the optional reverse transcription for PolyA and polyl-tailed libraries. ..

    Article Title: Keratinocyte–TRPV1 sensory neuron interactions in a genetically controllable mouse model of chronic neuropathic itch
    Article Snippet: .. The epidermis was separated from the whole skin by incubating in Trypsin-EDTA 0.15% for 45 min. Isolated cells from the epidermis and whole mRNA was extracted using an RNeasy Mini kit from Qiagen after which was reverse transcribed into cDNA using Superscript IV (ThermoFisher Cat # 18091200). qPCR analyses were carried out with gene specific primers and fluorescently labeled Taqman probes (ThermoFisher Scientific) for Tslp (Mm01157588_m1), Il33 (Mm00505403_m1), Edn1 (Mm00438659_m1), and Postn (Mm01284919_m1). .. Relative expression level was calculated using the 2 − ΔΔCT method. β-actin (Mm02619580_g1) was used as the internal control for each sample.

    Article Title: The role of transient receptor potential vanilloid 1 (TRPV1) in Candida albicans infection-induced oral burning sensation: Evidenced from mouse and zebrafish models
    Article Snippet: Sections were deparaffinized, rehydrated, and subjected to antigen retrieval in citrate buffer (pH 6.0) at 95 °C for 20 min. Endogenous peroxidase was blocked using 3 % hydrogen peroxide in methanol for 10 min, followed by blocking in 5 % BSA/PBS for 30 min. Primary antibody (p–NF–H, Thermo Fisher) was applied overnight at 4 °C, followed by incubation with a biotinylated secondary antibody for 30 min. Visualization was achieved using 3,3′-diaminobenzidine (DAB), and slides were counterstained, dehydrated, and mounted. .. Total RNA from zebrafish embryos was extracted with TRIzol reagent (Invitrogen, Waltham, MA, USA), reverse-transcribed using SuperScript IV (Thermo Fisher Scientific, Waltham, MA, USA), and analyzed via quantitative real-time polymerase chain reaction using PowerUp SYBR Green Master Mix (Thermo Fisher Scientific, Waltham, MA, USA). ..

    Article Title: Dissecting functional regulatory convergence over 160 million years of therian evolution
    Article Snippet: The eluted RNA was then treated again with Turbo DNase (AM1907, Thermo Fisher Scientific). .. We used an input of between 25-50 ug of RNA per replicate library for first-strand synthesis with Superscript IV (18090200, Thermo Fisher Scientific), with the reverse transcription primer ( Reverse_transcription_primer_R ). .. We additionally treated the first-strand synthesis product with 1 uL of RNAse A (7000 units) (Qiagen, 19101) to remove excess leftover RNA.

    Isolation:

    Article Title: Keratinocyte–TRPV1 sensory neuron interactions in a genetically controllable mouse model of chronic neuropathic itch
    Article Snippet: .. The epidermis was separated from the whole skin by incubating in Trypsin-EDTA 0.15% for 45 min. Isolated cells from the epidermis and whole mRNA was extracted using an RNeasy Mini kit from Qiagen after which was reverse transcribed into cDNA using Superscript IV (ThermoFisher Cat # 18091200). qPCR analyses were carried out with gene specific primers and fluorescently labeled Taqman probes (ThermoFisher Scientific) for Tslp (Mm01157588_m1), Il33 (Mm00505403_m1), Edn1 (Mm00438659_m1), and Postn (Mm01284919_m1). .. Relative expression level was calculated using the 2 − ΔΔCT method. β-actin (Mm02619580_g1) was used as the internal control for each sample.

    Real-time Polymerase Chain Reaction:

    Article Title: Keratinocyte–TRPV1 sensory neuron interactions in a genetically controllable mouse model of chronic neuropathic itch
    Article Snippet: .. The epidermis was separated from the whole skin by incubating in Trypsin-EDTA 0.15% for 45 min. Isolated cells from the epidermis and whole mRNA was extracted using an RNeasy Mini kit from Qiagen after which was reverse transcribed into cDNA using Superscript IV (ThermoFisher Cat # 18091200). qPCR analyses were carried out with gene specific primers and fluorescently labeled Taqman probes (ThermoFisher Scientific) for Tslp (Mm01157588_m1), Il33 (Mm00505403_m1), Edn1 (Mm00438659_m1), and Postn (Mm01284919_m1). .. Relative expression level was calculated using the 2 − ΔΔCT method. β-actin (Mm02619580_g1) was used as the internal control for each sample.

    Article Title: The role of transient receptor potential vanilloid 1 (TRPV1) in Candida albicans infection-induced oral burning sensation: Evidenced from mouse and zebrafish models
    Article Snippet: Sections were deparaffinized, rehydrated, and subjected to antigen retrieval in citrate buffer (pH 6.0) at 95 °C for 20 min. Endogenous peroxidase was blocked using 3 % hydrogen peroxide in methanol for 10 min, followed by blocking in 5 % BSA/PBS for 30 min. Primary antibody (p–NF–H, Thermo Fisher) was applied overnight at 4 °C, followed by incubation with a biotinylated secondary antibody for 30 min. Visualization was achieved using 3,3′-diaminobenzidine (DAB), and slides were counterstained, dehydrated, and mounted. .. Total RNA from zebrafish embryos was extracted with TRIzol reagent (Invitrogen, Waltham, MA, USA), reverse-transcribed using SuperScript IV (Thermo Fisher Scientific, Waltham, MA, USA), and analyzed via quantitative real-time polymerase chain reaction using PowerUp SYBR Green Master Mix (Thermo Fisher Scientific, Waltham, MA, USA). ..

    Labeling:

    Article Title: Keratinocyte–TRPV1 sensory neuron interactions in a genetically controllable mouse model of chronic neuropathic itch
    Article Snippet: .. The epidermis was separated from the whole skin by incubating in Trypsin-EDTA 0.15% for 45 min. Isolated cells from the epidermis and whole mRNA was extracted using an RNeasy Mini kit from Qiagen after which was reverse transcribed into cDNA using Superscript IV (ThermoFisher Cat # 18091200). qPCR analyses were carried out with gene specific primers and fluorescently labeled Taqman probes (ThermoFisher Scientific) for Tslp (Mm01157588_m1), Il33 (Mm00505403_m1), Edn1 (Mm00438659_m1), and Postn (Mm01284919_m1). .. Relative expression level was calculated using the 2 − ΔΔCT method. β-actin (Mm02619580_g1) was used as the internal control for each sample.

    Random Hexamer:

    Article Title: Use of capture based metagenomic to assess human enteric virus diversity in sewage and shellfish samples.
    Article Snippet: After elution from the magnetic silica to facilitate the subsequent washing steps, the NAs were treated with 25 U TURBO DNase (Ambion, Thermo Fisher Scientific, France) for 30 min at 37 ◦C before a final concentration step using the RNA Clean Concentrator kit (Zymo Research, Irvine, CA, United States). .. cDNA was prepared using Superscript IV (Invitrogen, Thermo Fisher Scientific, France) and random hexamer (New England Biolabs (NEB), USA) for each sewage sample extract and three cDNA synthesis from each NA extract for shellfish samples. .. At this step a negative control, in the form of sterile RNase-free water (molecular-grade water Merck Millipore cat n◦H20MB1006), was treated in parallel for all different library's preparation kits.

    cDNA Synthesis:

    Article Title: Use of capture based metagenomic to assess human enteric virus diversity in sewage and shellfish samples.
    Article Snippet: After elution from the magnetic silica to facilitate the subsequent washing steps, the NAs were treated with 25 U TURBO DNase (Ambion, Thermo Fisher Scientific, France) for 30 min at 37 ◦C before a final concentration step using the RNA Clean Concentrator kit (Zymo Research, Irvine, CA, United States). .. cDNA was prepared using Superscript IV (Invitrogen, Thermo Fisher Scientific, France) and random hexamer (New England Biolabs (NEB), USA) for each sewage sample extract and three cDNA synthesis from each NA extract for shellfish samples. .. At this step a negative control, in the form of sterile RNase-free water (molecular-grade water Merck Millipore cat n◦H20MB1006), was treated in parallel for all different library's preparation kits.

    SYBR Green Assay:

    Article Title: The role of transient receptor potential vanilloid 1 (TRPV1) in Candida albicans infection-induced oral burning sensation: Evidenced from mouse and zebrafish models
    Article Snippet: Sections were deparaffinized, rehydrated, and subjected to antigen retrieval in citrate buffer (pH 6.0) at 95 °C for 20 min. Endogenous peroxidase was blocked using 3 % hydrogen peroxide in methanol for 10 min, followed by blocking in 5 % BSA/PBS for 30 min. Primary antibody (p–NF–H, Thermo Fisher) was applied overnight at 4 °C, followed by incubation with a biotinylated secondary antibody for 30 min. Visualization was achieved using 3,3′-diaminobenzidine (DAB), and slides were counterstained, dehydrated, and mounted. .. Total RNA from zebrafish embryos was extracted with TRIzol reagent (Invitrogen, Waltham, MA, USA), reverse-transcribed using SuperScript IV (Thermo Fisher Scientific, Waltham, MA, USA), and analyzed via quantitative real-time polymerase chain reaction using PowerUp SYBR Green Master Mix (Thermo Fisher Scientific, Waltham, MA, USA). ..

    other:

    Article Title: Discovery of FoTO1 and Taxol genes enables biosynthesis of baccatin III.
    Article Snippet: Candidate genes were amplified from T. media gDNA or cDNA (generated with SuperScript IV, Thermo Fisher Scientific) by PCR (PrimeStar, Takara Bio R045B, primers in Supplementary Table 13), and the PCR products were ligated with AgeI- and XhoI- (New England Biolabs) linearized pEAQ-HT vector66 using HiFi DNA assembly mix (New England Biolabs).



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