qpcr conditions Search Results


qpcr reaction conditions  (Ribobio co)
90
Ribobio co qpcr reaction conditions
Qpcr Reaction Conditions, supplied by Ribobio co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rt-qpcr data per experimental condition from hkls  (RStudio)
90
RStudio rt-qpcr data per experimental condition from hkls
Rt Qpcr Data Per Experimental Condition From Hkls, supplied by RStudio, 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/result/rt-qpcr data per experimental condition from hkls/product/RStudio
Average 90 stars, based on 1 article reviews
rt-qpcr data per experimental condition from hkls - by Bioz Stars, 2026-05
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qpcr conditions  (Lallemand inc)
90
Lallemand inc qpcr conditions
Qpcr Conditions, supplied by Lallemand inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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qpcr conditions - by Bioz Stars, 2026-05
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qpcr amplification conditions ep primers  (Promega)
90
Promega qpcr amplification conditions ep primers
Relative quantification of 10 efflux pump genes in Mycobacterium tuberculosis H37Rv, assessed by reverse transcription quantitative <t>PCR</t> <t>(RT-qPCR)</t> after 24 h of RIF (1/2 MIC, 0.002 μg/ml), piperine (1/2 MIC, 62.5 μg/ml), or RIF plus piperine (1/2 MIC) exposure. Results were normalized to 16S rRNA and calculated by the 2−ΔΔCT method. * and ** indicate P < 0.05 and P < 0.001, respectively, in comparison with the control sample. Horizontal brackets indicate statistical difference (P < 0.05) comparing the rates of given genes in samples exposed to RIF and RIF plus piperine.
Qpcr Amplification Conditions Ep Primers, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
qpcr amplification conditions ep primers - by Bioz Stars, 2026-05
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Relative quantification of 10 efflux pump genes in Mycobacterium tuberculosis H37Rv, assessed by reverse transcription quantitative PCR (RT-qPCR) after 24 h of RIF (1/2 MIC, 0.002 μg/ml), piperine (1/2 MIC, 62.5 μg/ml), or RIF plus piperine (1/2 MIC) exposure. Results were normalized to 16S rRNA and calculated by the 2−ΔΔCT method. * and ** indicate P < 0.05 and P < 0.001, respectively, in comparison with the control sample. Horizontal brackets indicate statistical difference (P < 0.05) comparing the rates of given genes in samples exposed to RIF and RIF plus piperine.

Journal: Antimicrobial Agents and Chemotherapy

Article Title: Possible Binding of Piperine in Mycobacterium tuberculosis RNA Polymerase and Rifampin Synergism

doi: 10.1128/AAC.02520-18

Figure Lengend Snippet: Relative quantification of 10 efflux pump genes in Mycobacterium tuberculosis H37Rv, assessed by reverse transcription quantitative PCR (RT-qPCR) after 24 h of RIF (1/2 MIC, 0.002 μg/ml), piperine (1/2 MIC, 62.5 μg/ml), or RIF plus piperine (1/2 MIC) exposure. Results were normalized to 16S rRNA and calculated by the 2−ΔΔCT method. * and ** indicate P < 0.05 and P < 0.001, respectively, in comparison with the control sample. Horizontal brackets indicate statistical difference (P < 0.05) comparing the rates of given genes in samples exposed to RIF and RIF plus piperine.

Article Snippet: Quantitative PCR (qPCR) amplification conditions varied according to EP primers (Promega, USA) ( ).

Techniques: Quantitative Proteomics, Reverse Transcription, Real-time Polymerase Chain Reaction, Quantitative RT-PCR, Comparison, Control

Relative quantification of 12 efflux pump genes in susceptible isolate of Mycobacterium tuberculosis 47S, assessed by RT-qPCR after 24 h of RIF (1/2 MIC, 0.002 μg/ml), piperine (1/2 MIC, 62.5 μg/ml), or RIF plus piperine (1/2 MIC) exposure. Results were normalized to 16S rRNA and calculated by the 2−ΔΔCT method. * and ** indicate P < 0.05 and P < 0.001, respectively, in comparison with the control sample. Horizontal brackets indicate statistical difference (P < 0.05) comparing the rates of given genes in samples exposed to RIF and RIF plus piperine.

Journal: Antimicrobial Agents and Chemotherapy

Article Title: Possible Binding of Piperine in Mycobacterium tuberculosis RNA Polymerase and Rifampin Synergism

doi: 10.1128/AAC.02520-18

Figure Lengend Snippet: Relative quantification of 12 efflux pump genes in susceptible isolate of Mycobacterium tuberculosis 47S, assessed by RT-qPCR after 24 h of RIF (1/2 MIC, 0.002 μg/ml), piperine (1/2 MIC, 62.5 μg/ml), or RIF plus piperine (1/2 MIC) exposure. Results were normalized to 16S rRNA and calculated by the 2−ΔΔCT method. * and ** indicate P < 0.05 and P < 0.001, respectively, in comparison with the control sample. Horizontal brackets indicate statistical difference (P < 0.05) comparing the rates of given genes in samples exposed to RIF and RIF plus piperine.

Article Snippet: Quantitative PCR (qPCR) amplification conditions varied according to EP primers (Promega, USA) ( ).

Techniques: Quantitative Proteomics, Quantitative RT-PCR, Comparison, Control

Relative regulation of 12 efflux pump genes in a multidrug-resistant isolate of Mycobacterium tuberculosis 71A, assessed by RT-qPCR after 24 h of RIF (1/2 MIC, 25 μg/ml), piperine (1/2 MIC, 62.5 μg/ml), or RIF plus piperine (1/2 MIC) exposure. Results were normalized to 16S rRNA and calculated by the 2−ΔΔCT method. * and ** indicate P < 0.05 and P < 0.001, respectively, in comparison with the control sample. Horizontal brackets indicate statistical difference (P < 0.05) comparing the rates of given genes in samples exposed to RIF and RIF and piperine.

Journal: Antimicrobial Agents and Chemotherapy

Article Title: Possible Binding of Piperine in Mycobacterium tuberculosis RNA Polymerase and Rifampin Synergism

doi: 10.1128/AAC.02520-18

Figure Lengend Snippet: Relative regulation of 12 efflux pump genes in a multidrug-resistant isolate of Mycobacterium tuberculosis 71A, assessed by RT-qPCR after 24 h of RIF (1/2 MIC, 25 μg/ml), piperine (1/2 MIC, 62.5 μg/ml), or RIF plus piperine (1/2 MIC) exposure. Results were normalized to 16S rRNA and calculated by the 2−ΔΔCT method. * and ** indicate P < 0.05 and P < 0.001, respectively, in comparison with the control sample. Horizontal brackets indicate statistical difference (P < 0.05) comparing the rates of given genes in samples exposed to RIF and RIF and piperine.

Article Snippet: Quantitative PCR (qPCR) amplification conditions varied according to EP primers (Promega, USA) ( ).

Techniques: Quantitative RT-PCR, Comparison, Control