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Starter templates

Compare the starter assays before describing your own. Every example below is computed from the same frozen fixtures the test suite verifies — no numbers are invented.

  • BCA protein assay

    Ready

    Quantify protein concentrations from a BCA standard curve on a 96-well plate — replicate means, R², and out-of-range flags included.

    01230123protein (mg/mL)A562

    C3/D3 · 0.2476 A562 → 0.2368 mg/mL

    A562

    Fit
    quadratic
    R²
    0.999987
    Unknowns
    40
    Range (mg/mL)
    0.125–2

    Opens with built-in sample data.

  • Bradford protein assay

    Ready

    Quantify protein concentrations from a Bradford (Coomassie) standard curve at A595 — replicate means, R², and out-of-range flags included.

    00.511.50123protein (mg/mL)A595

    Unknown 02 · 0.1425 A595 → 0.212 mg/mL

    A595

    Fit
    quadratic
    R²
    0.999988
    Unknowns
    40
    Range (mg/mL)
    0.125–2

    Opens with built-in sample data.

  • ELISA 4PL

    Ready

    Fit a 4-parameter logistic standard curve to OD450 readings and back-solve sample concentrations in ng/mL.

    012341101001kconcentration (ng/mL), logOD450

    sample02 · 0.6022 OD450 → 5.81 ng/mL

    OD450

    Curve
    4PL
    R²
    0.999992
    Unknowns
    40
    Range (ng/mL)
    3.125–100

    Opens with built-in sample data.

  • Dose-response IC50

    Ready

    Fit a 4PL dose-response curve over a µM dose ladder and read off IC50 with a show-the-math line for every sample.

    00.511.520.0010.010.1110100dose (µM), logresponse

    E4/F4 · 1.321 response → 0.04918 µM

    response

    Curve
    4PL
    R²
    0.999998
    Unknowns
    12
    IC50 (µM)
    1.252721

    Opens with built-in sample data.

  • qPCR ΔΔCt

    Ready

    Relative quantification by the ΔΔCt (Livak) method — technical-replicate means, ΔCt against a reference gene, and fold change against a calibrator sample, with undetermined wells and replicate spread flagged.

    0510fold change (×)Treated-A IL6Treated-A MYCTreated-B IL6Treated-B MYCControl

    Treated-A IL6 · 4× · ΔΔCt -2 · replicate range 3.36–4.76

    Reference gene
    GAPDH
    Calibrator
    Control
    Treated-A IL6 fold change
    4
    Treated-A MYC fold change
    0.5
    Treated-B IL6 fold change
    8
    Treated-B MYC fold change
    1

    Opens with built-in sample data.

  • Michaelis–Menten kinetics

    Ready

    Initial rates from kinetic reads, nonlinear Vmax/Km fit with standard errors, Lineweaver–Burk reference plot.

    00.10.20.305101520[S] (mM)rate

    Measured · 0.1 mM → 0.02666 AU/min

    mM

    Vmax (AU/min)
    0.239947
    Km (mM)
    0.800293
    R²
    0.999996
    Series fitted
    8

    Opens with built-in sample data.

  • Bacterial growth curves (OD600)

    Ready

    Blank correction, log-phase detection, growth rate, doubling time, lag time, per-well summary table.

    00.511.5growth rate µ (1/h)A1A3A5A7–A9––A11

    A1 · 0.9091 1/h · doubling 0.762 h · lag 1.8 h

    Wells summarized
    12
    Log-phase fits
    9
    µ range (1/h)
    0.909095–1.303832
    Doubling range (h)
    0.531623–0.762458

    Opens with built-in sample data.

  • Cell viability (MTT / resazurin)

    Ready

    Read percent viability for every treatment group against the untreated control — background subtraction, replicate CV, and a dose + %viability hand-off for the IC50 tool included.

    050100150viability (%)0102030405060708control

    dose-01 · 99.08% · corrected mean 0.9425 · CV 0.221%

    Control
    100%
    Background
    0.049013
    Groups
    8
    Lowest viability
    8.612126%

    Opens with built-in sample data.

  • Generic standard curve

    Ready

    Fit any assay’s standards with linear, quadratic, or 4PL chosen by AIC, back-calculate unknown concentrations, and flag out-of-range results.

    01230.1110100concentration, logsignal

    U1 · 0.5634 signal → 0.8 concentration

    signal

    Model (by AIC)
    4PL
    R²
    1
    Unknowns
    6
    Extrapolated
    1

    Opens with built-in sample data.

  • Western blot densitometry

    Ready

    Background-subtract ImageJ/Fiji band intensities, normalize to a loading control by lane label, and report fold change vs control with replicate stats.

    00.511.52fold change (×)C-1C-2T-1T-2control mean

    C-1 · 1.333× · Control

    Lanes
    4
    Conditions
    2
    Treatment fold change
    1.2

    Opens with built-in sample data.