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non-linear regression one phase exponential decay curve fitting  (GraphPad Software Inc)

 
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    GraphPad Software Inc non-linear regression one phase exponential decay curve fitting
    Non Linear Regression One Phase Exponential Decay Curve Fitting, 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/non-linear regression one phase exponential decay curve fitting/product/GraphPad Software Inc
    Average 90 stars, based on 1 article reviews
    non-linear regression one phase exponential decay curve fitting - by Bioz Stars, 2026-03
    90/100 stars

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    GraphPad Software Inc non-linear regression one phase exponential decay curve fitting
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    GraphPad Software Inc non-linear regression curve fitting for one phase exponential decay
    (A) Inactivation of the SCF E3 ubiquitin ligase does not cause increased Cln2 protein levels in rts1 Δ cells. Cells of the indicated genotypes were released from an α factor arrest into pre-warmed media at 37°C. Levels of Cln2-3XHA protein were monitored by Western blotting. (B) rts1 Δ does not decrease the half-life of the Cln2 protein. GAL1-3XHA-CLN2 and GAL1-3XHA-CLN2 rts1 Δ cells were grown overnight at room temperature in YEP media containing 2% glycerol/ethanol. A burst of CLN2 transcription was triggered by washing the cells into YEP +2% galactose for 1 hour. At time = 0, CLN2 transcription was turned off by washing cells into YEPD media. Samples were collected at t = 0, 5, 10, 15, 20, 30, 45, 60, and 120 minutes, and quantitative Western blotting was used to determine Cln2 levels. The half-life of Cln2 protein was calculated using a standard curve fitted for one phase <t>exponential</t> decay. The half-life of Cln2 was 9.6±2.0 minutes in wild type cells and 10.8±2.4 minutes in rts1 Δ cells (n = 3).
    Non Linear Regression Curve Fitting For One Phase Exponential Decay, 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
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    Average 90 stars, based on 1 article reviews
    non-linear regression curve fitting for one phase exponential decay - by Bioz Stars, 2026-03
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    (A) Inactivation of the SCF E3 ubiquitin ligase does not cause increased Cln2 protein levels in rts1 Δ cells. Cells of the indicated genotypes were released from an α factor arrest into pre-warmed media at 37°C. Levels of Cln2-3XHA protein were monitored by Western blotting. (B) rts1 Δ does not decrease the half-life of the Cln2 protein. GAL1-3XHA-CLN2 and GAL1-3XHA-CLN2 rts1 Δ cells were grown overnight at room temperature in YEP media containing 2% glycerol/ethanol. A burst of CLN2 transcription was triggered by washing the cells into YEP +2% galactose for 1 hour. At time = 0, CLN2 transcription was turned off by washing cells into YEPD media. Samples were collected at t = 0, 5, 10, 15, 20, 30, 45, 60, and 120 minutes, and quantitative Western blotting was used to determine Cln2 levels. The half-life of Cln2 protein was calculated using a standard curve fitted for one phase exponential decay. The half-life of Cln2 was 9.6±2.0 minutes in wild type cells and 10.8±2.4 minutes in rts1 Δ cells (n = 3).

    Journal: PLoS Genetics

    Article Title: The Rts1 Regulatory Subunit of Protein Phosphatase 2A Is Required for Control of G1 Cyclin Transcription and Nutrient Modulation of Cell Size

    doi: 10.1371/journal.pgen.1000727

    Figure Lengend Snippet: (A) Inactivation of the SCF E3 ubiquitin ligase does not cause increased Cln2 protein levels in rts1 Δ cells. Cells of the indicated genotypes were released from an α factor arrest into pre-warmed media at 37°C. Levels of Cln2-3XHA protein were monitored by Western blotting. (B) rts1 Δ does not decrease the half-life of the Cln2 protein. GAL1-3XHA-CLN2 and GAL1-3XHA-CLN2 rts1 Δ cells were grown overnight at room temperature in YEP media containing 2% glycerol/ethanol. A burst of CLN2 transcription was triggered by washing the cells into YEP +2% galactose for 1 hour. At time = 0, CLN2 transcription was turned off by washing cells into YEPD media. Samples were collected at t = 0, 5, 10, 15, 20, 30, 45, 60, and 120 minutes, and quantitative Western blotting was used to determine Cln2 levels. The half-life of Cln2 protein was calculated using a standard curve fitted for one phase exponential decay. The half-life of Cln2 was 9.6±2.0 minutes in wild type cells and 10.8±2.4 minutes in rts1 Δ cells (n = 3).

    Article Snippet: Non-linear regression curve fitting for one phase exponential decay was carried out using GraphPad Prism version 4.00 for Mac .

    Techniques: Ubiquitin Proteomics, Western Blot