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gene exp prm1 ss03383652 u1  (Thermo Fisher)


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    Thermo Fisher gene exp prm1 ss03383652 u1
    Gene Exp Prm1 Ss03383652 U1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gene+exp+prm1+ss03383652+u1/Gene+Exp%2E+PRM1%2C+Ss03383652_u1/pm41572268-110-19-13
    Average 94 stars, based on 1 article reviews
    gene exp prm1 ss03383652 u1 - by Bioz Stars, 2026-11
    94/100 stars

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    Related Articles

    Gene Expression:

    Article Title: Exploring ethical dilemmas in the care of pregnant women in Ghana: a case of "maternal-foetal conflicts in a peri-urban hospital in Ghana".
    Article Snippet: .. Similarly, absence of DNA contamination was confirmed using PRM1 TaqManTM Gene Expression Assay (Applied Biosystems, CA, USA, Assay ID: Ss03383652_u1) by comparing RT-qPCR reactions with and without reverse transcriptase (-RT controls) following the protocol described in [30]. .. Using 4 μl total RNA (8.8-61.2 ng), rRNA was blocked from cDNA extension using the QiaSeq FastSelect HMR reagents (Qiagen, Germany), following the “-rRNA and/or -Globin with the NEBNext Ultra II Directional Library Prep Kit” procedure in the manufacturer ́s handbook v12/21, including the “partially degraded RNA (RIN 2-6)” variations.

    Article Title: Sperm RNA landscape during sexual maturation in Duroc boars
    Article Snippet: .. Similarly, absence of DNA contamination was confirmed using PRM1 TaqManTM Gene Expression Assay (Applied Biosystems, CA, USA, Assay ID: Ss03383652_u1) by comparing RT-qPCR reactions with and without reverse transcriptase (-RT controls) following the protocol described in [ ]. .. Using 4 μl total RNA (8.8–61.2 ng), rRNA was blocked from cDNA extension using the QiaSeq FastSelect HMR reagents (Qiagen, Germany), following the “-rRNA and/or -Globin with the NEBNext Ultra II Directional Library Prep Kit” procedure in the manufacturer ́s handbook v12/21, including the “partially degraded RNA (RIN 2–6)” variations.

    Quantitative RT-PCR:

    Article Title: Exploring ethical dilemmas in the care of pregnant women in Ghana: a case of "maternal-foetal conflicts in a peri-urban hospital in Ghana".
    Article Snippet: .. Similarly, absence of DNA contamination was confirmed using PRM1 TaqManTM Gene Expression Assay (Applied Biosystems, CA, USA, Assay ID: Ss03383652_u1) by comparing RT-qPCR reactions with and without reverse transcriptase (-RT controls) following the protocol described in [30]. .. Using 4 μl total RNA (8.8-61.2 ng), rRNA was blocked from cDNA extension using the QiaSeq FastSelect HMR reagents (Qiagen, Germany), following the “-rRNA and/or -Globin with the NEBNext Ultra II Directional Library Prep Kit” procedure in the manufacturer ́s handbook v12/21, including the “partially degraded RNA (RIN 2-6)” variations.

    Article Title: Sperm RNA landscape during sexual maturation in Duroc boars
    Article Snippet: .. Similarly, absence of DNA contamination was confirmed using PRM1 TaqManTM Gene Expression Assay (Applied Biosystems, CA, USA, Assay ID: Ss03383652_u1) by comparing RT-qPCR reactions with and without reverse transcriptase (-RT controls) following the protocol described in [ ]. .. Using 4 μl total RNA (8.8–61.2 ng), rRNA was blocked from cDNA extension using the QiaSeq FastSelect HMR reagents (Qiagen, Germany), following the “-rRNA and/or -Globin with the NEBNext Ultra II Directional Library Prep Kit” procedure in the manufacturer ́s handbook v12/21, including the “partially degraded RNA (RIN 2–6)” variations.

    Reverse Transcription:

    Article Title: Exploring ethical dilemmas in the care of pregnant women in Ghana: a case of "maternal-foetal conflicts in a peri-urban hospital in Ghana".
    Article Snippet: .. Similarly, absence of DNA contamination was confirmed using PRM1 TaqManTM Gene Expression Assay (Applied Biosystems, CA, USA, Assay ID: Ss03383652_u1) by comparing RT-qPCR reactions with and without reverse transcriptase (-RT controls) following the protocol described in [30]. .. Using 4 μl total RNA (8.8-61.2 ng), rRNA was blocked from cDNA extension using the QiaSeq FastSelect HMR reagents (Qiagen, Germany), following the “-rRNA and/or -Globin with the NEBNext Ultra II Directional Library Prep Kit” procedure in the manufacturer ́s handbook v12/21, including the “partially degraded RNA (RIN 2-6)” variations.

    Article Title: Sperm RNA landscape during sexual maturation in Duroc boars
    Article Snippet: .. Similarly, absence of DNA contamination was confirmed using PRM1 TaqManTM Gene Expression Assay (Applied Biosystems, CA, USA, Assay ID: Ss03383652_u1) by comparing RT-qPCR reactions with and without reverse transcriptase (-RT controls) following the protocol described in [ ]. .. Using 4 μl total RNA (8.8–61.2 ng), rRNA was blocked from cDNA extension using the QiaSeq FastSelect HMR reagents (Qiagen, Germany), following the “-rRNA and/or -Globin with the NEBNext Ultra II Directional Library Prep Kit” procedure in the manufacturer ́s handbook v12/21, including the “partially degraded RNA (RIN 2–6)” variations.



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