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exponential growth equation (nonlinear fit)  (GraphPad Software Inc)

 
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    GraphPad Software Inc exponential growth equation (nonlinear fit)
    Exponential Growth Equation (Nonlinear Fit), supplied by GraphPad Software Inc, 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/exponential growth equation (nonlinear fit)/product/GraphPad Software Inc
    Average 90 stars, based on 1 article reviews
    exponential growth equation (nonlinear fit) - by Bioz Stars, 2026-03
    90/100 stars

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    qRT-PCR results verifying RNA-seq and examining if proteomics targets have altered transcript levels. Wild-type NZ131, Δ rgg2 , and Δ rgg3 strains were grown in biological triplicate with or without 100 nM SHP peptide (indicated by + or – sign below each graph) and RNA was harvested late exponential phase. RNA was processed for qRT-PCR and transcript levels were determine relative to the gyrA reference gene. Significance of transcript level changes were determined using a One-way ANOVA with Multiple Comparisons Post-test. *, P < 0.05; **, P < 0.005; ****, P < 0.0005; ns, non-significant. For further experimental details, see Materials and Methods . A) Relative transcript levels of spy49_0450 (aroE.2) . B) Relative transcript levels of stcA ( spy49_0414c ). C) Relative transcript levels of slo ( spy49_0146 ). D) Relative transcript levels of sfbX49 ( spy49_1683c ). E) Relative transcript levels of upp ( spy49_0322 ). F) Relative transcript levels of spy49_0877 .

    Journal: bioRxiv

    Article Title: The proteomic and transcriptomic landscapes altered by Rgg2/3 activity in Streptococcus pyogenes

    doi: 10.1101/2022.05.06.490990

    Figure Lengend Snippet: qRT-PCR results verifying RNA-seq and examining if proteomics targets have altered transcript levels. Wild-type NZ131, Δ rgg2 , and Δ rgg3 strains were grown in biological triplicate with or without 100 nM SHP peptide (indicated by + or – sign below each graph) and RNA was harvested late exponential phase. RNA was processed for qRT-PCR and transcript levels were determine relative to the gyrA reference gene. Significance of transcript level changes were determined using a One-way ANOVA with Multiple Comparisons Post-test. *, P < 0.05; **, P < 0.005; ****, P < 0.0005; ns, non-significant. For further experimental details, see Materials and Methods . A) Relative transcript levels of spy49_0450 (aroE.2) . B) Relative transcript levels of stcA ( spy49_0414c ). C) Relative transcript levels of slo ( spy49_0146 ). D) Relative transcript levels of sfbX49 ( spy49_1683c ). E) Relative transcript levels of upp ( spy49_0322 ). F) Relative transcript levels of spy49_0877 .

    Article Snippet: Data was plotted and doubling times were calculated by taking OD 600 s ∼0.015 – 0.9 and performing a Nonlinear regression analysis with Exponential growth equation fitting with Graph Pad Prism 9.2.0 (GraphPad Software).

    Techniques: Quantitative RT-PCR, RNA Sequencing