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trap primer mixture  (TaKaRa)


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    Structured Review

    TaKaRa trap primer mixture
    Trap Primer Mixture, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 1452 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/trap+primer+mix/Universal+Primer+Mix/10__1021_slash_acs__jmedchem__0c01656-312-51-72
    Average 99 stars, based on 1452 article reviews
    trap primer mixture - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Incubation:

    Article Title: Design, synthesis of 4,5-diazafluorene derivatives and their anticancer activity via targeting telomeric DNA G-quadruplex
    Article Snippet: In our work, 19 novel 4,5-diazafluorene derivatives (11a-d, 12a-d, 13a-d, 14a-c, 15c, 16ac) bearing a 1,3-disubstituted pyrazol/thioxothiazolidinone or thioxothiazolidinone-oxadiazole moieties were designed, synthesized, preliminarily explored for their antitumor activities and in vitro mechanism.. All compounds showed different values of antiproliferative activity against A549, AGS, HepG2 and MCF-7 cell lines through CCK-8.. Especially, the compound 14c exhibited the strongest activity and best selectivity against A549 cells with an IC50 1.13 μM and an SI value of 7.01 relative to MRC-5 cells, which was better than cisplatin (SI = 1.80) as a positive control.

    Polymerase Chain Reaction:

    Article Title: TERT polymorphisms modify the risk of acute lymphoblastic leukemia in Chinese children.
    Article Snippet: Telomerase activity was measured using TRAPeze telomerase detection kit (S7700; Millipore, Bedford, MA) according to manufacturer instructions. .. Briefly, lysates containing 300 ng protein were added into the PCR master mix containing 10× telomeric repeat amplification protocol (TRAP) reaction buffer, 50× deoxynucleoside triphosphate mix, TS primer, TRAP primer mix and TaKaRa Ex Taq Hot Start polymerase. .. PCR conditions were one cycle at 30°C for 30 min, 33 cycles at 94°C for 30 s, 59°C for 30 s and 72°C for 1 min. PCR TRAP products were loaded and ran on a 12.5% non-denaturing polyacrylamide gel electrophoresis for 30 min at 250 V. After electrophoresis, the gel was stained with SYBR Green (Invitrogen) for 30 min and destained for 20 min in deionized water.

    Article Title: A mRNA-Responsive G-Quadruplex-Based Drug Release System.
    Article Snippet: .. In the second step, telomerase reaction products were amplified in a 10-μL PCR reaction mixture containing 50-fold diluted telomerase mixture, 0.2 μL TS primer, 0.2 μL TRAP primer mix, 1 × dNTP mix, 1 × LA Taq polymerase buffer, and LA Taq polymerase (Takara Bio). ..

    Article Title: A mRNA-Responsive G-Quadruplex-Based Drug Release System
    Article Snippet: .. In the second step, telomerase reaction products were amplified in a 10-μL PCR reaction mixture containing 50-fold diluted telomerase mixture, 0.2 μL TS primer, 0.2 μL TRAP primer mix, 1 × dNTP mix, 1 × LA Taq polymerase buffer, and LA Taq polymerase (Takara Bio). ..

    Article Title: In vitro assays predictive of telomerase inhibitory effect of G-quadruplex ligands in cell nuclei.
    Article Snippet: G-quadruplex-binding and telomerase-inhibiting capacities of G-quadruplex ligands were examined under a cell nuclei-mimicking condition including excess double-stranded DNA (λ DNA) and molecular crowding cosolute (PEG 200).. Under the cell nuclei-mimicking condition, a cationic porphyrin (TMPyP4) did not bind to the G-quadruplex despite the high affinity (Ka = 3.6 × 10 6 M−1) under a diluted condition without λ DNA and PEG 200.. Correspondingly, TMPyP4 inhibited telomerase activity under the diluted condition (IC50 = 1.6 μM) but not under the cell nuclei-mimicking condition.

    Amplification:

    Article Title: TERT polymorphisms modify the risk of acute lymphoblastic leukemia in Chinese children.
    Article Snippet: Telomerase activity was measured using TRAPeze telomerase detection kit (S7700; Millipore, Bedford, MA) according to manufacturer instructions. .. Briefly, lysates containing 300 ng protein were added into the PCR master mix containing 10× telomeric repeat amplification protocol (TRAP) reaction buffer, 50× deoxynucleoside triphosphate mix, TS primer, TRAP primer mix and TaKaRa Ex Taq Hot Start polymerase. .. PCR conditions were one cycle at 30°C for 30 min, 33 cycles at 94°C for 30 s, 59°C for 30 s and 72°C for 1 min. PCR TRAP products were loaded and ran on a 12.5% non-denaturing polyacrylamide gel electrophoresis for 30 min at 250 V. After electrophoresis, the gel was stained with SYBR Green (Invitrogen) for 30 min and destained for 20 min in deionized water.

    Article Title: A mRNA-Responsive G-Quadruplex-Based Drug Release System.
    Article Snippet: .. In the second step, telomerase reaction products were amplified in a 10-μL PCR reaction mixture containing 50-fold diluted telomerase mixture, 0.2 μL TS primer, 0.2 μL TRAP primer mix, 1 × dNTP mix, 1 × LA Taq polymerase buffer, and LA Taq polymerase (Takara Bio). ..

    Article Title: A mRNA-Responsive G-Quadruplex-Based Drug Release System
    Article Snippet: .. In the second step, telomerase reaction products were amplified in a 10-μL PCR reaction mixture containing 50-fold diluted telomerase mixture, 0.2 μL TS primer, 0.2 μL TRAP primer mix, 1 × dNTP mix, 1 × LA Taq polymerase buffer, and LA Taq polymerase (Takara Bio). ..

    Article Title: In vitro assays predictive of telomerase inhibitory effect of G-quadruplex ligands in cell nuclei.
    Article Snippet: G-quadruplex-binding and telomerase-inhibiting capacities of G-quadruplex ligands were examined under a cell nuclei-mimicking condition including excess double-stranded DNA (λ DNA) and molecular crowding cosolute (PEG 200).. Under the cell nuclei-mimicking condition, a cationic porphyrin (TMPyP4) did not bind to the G-quadruplex despite the high affinity (Ka = 3.6 × 10 6 M−1) under a diluted condition without λ DNA and PEG 200.. Correspondingly, TMPyP4 inhibited telomerase activity under the diluted condition (IC50 = 1.6 μM) but not under the cell nuclei-mimicking condition.

    TRAP Assay:

    Article Title: In vitro assays predictive of telomerase inhibitory effect of G-quadruplex ligands in cell nuclei.
    Article Snippet: G-quadruplex-binding and telomerase-inhibiting capacities of G-quadruplex ligands were examined under a cell nuclei-mimicking condition including excess double-stranded DNA (λ DNA) and molecular crowding cosolute (PEG 200).. Under the cell nuclei-mimicking condition, a cationic porphyrin (TMPyP4) did not bind to the G-quadruplex despite the high affinity (Ka = 3.6 × 10 6 M−1) under a diluted condition without λ DNA and PEG 200.. Correspondingly, TMPyP4 inhibited telomerase activity under the diluted condition (IC50 = 1.6 μM) but not under the cell nuclei-mimicking condition.

    Electrophoresis:

    Article Title: In vitro assays predictive of telomerase inhibitory effect of G-quadruplex ligands in cell nuclei.
    Article Snippet: G-quadruplex-binding and telomerase-inhibiting capacities of G-quadruplex ligands were examined under a cell nuclei-mimicking condition including excess double-stranded DNA (λ DNA) and molecular crowding cosolute (PEG 200).. Under the cell nuclei-mimicking condition, a cationic porphyrin (TMPyP4) did not bind to the G-quadruplex despite the high affinity (Ka = 3.6 × 10 6 M−1) under a diluted condition without λ DNA and PEG 200.. Correspondingly, TMPyP4 inhibited telomerase activity under the diluted condition (IC50 = 1.6 μM) but not under the cell nuclei-mimicking condition.



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