Toxicity Predictor

Toxicity Predictor

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ADME & Toxicity Predictor

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LCMS

LCMS

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🧪 LCMS Data Analyzer + m/z Calculator

Upload your LCMS CSV or XLSX file below

📊 Total Ion Chromatogram

🔍 Detected Peaks

Peak #	RT (min)	m/z	Intensity	Action

⚡ m/z Calculator (Common Adducts)

Selected m/z:

Adduct	Theoretical m/z	Neutral Mass (M)

Troubleshooting Tip: If results still don't appear after upload, try a simple .csv file first (not .xlsx). Make sure the file has columns like RT, m/z, Intensity.

LCMS Analyzer

LCMS Analyzer

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🧪 LCMS Data Analyzer

Upload your LCMS CSV or XLSX file and analyze it directly on this page

📊 Total Ion Chromatogram (TIC)

🔍 Detected Peaks

Peak #	Retention Time (min)	m/z	Intensity

How to use: Upload your LCMS export file. The tool will automatically plot the chromatogram and detect major peaks.
For compound prediction, copy the m/z value and use it in PubChem or specialized software.

FTIR Peak Analyzer

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📊

FTIR Peak Analyzer

Instantly identify functional groups from your IR spectrum peaks

🔬 Peak Position (cm⁻¹) Typical range: 400–4000 cm⁻¹

📌 Peak Type / Appearance Select the observed intensity & shape

Enter a peak value & select its type above
→ Click Analyze to get Group & Class

Based on standard FTIR correlation table • Data covers alcohols, carbonyls, amines, alkenes, aromatics & more
Tip: Peak ranges are approximate. Multiple matches may appear if your observed peak fits several possibilities.

Serial Dilution Planner (Microbiology/Biotech)

Serial Dilution Planner (Microbiology/Biotech)

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🧪 Serial Dilution Planner

Stock Concentration (M or CFU/mL) Desired Final Concentration Total Volume per tube (mL) Number of Dilution Steps

Transformation Efficiency Calculator

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🧪 Transformation Efficiency Calculator

CFU counted on plate Dilution factor (e.g. 10⁴ = 10000) DNA used (ng)

PCR Yield & Efficiency Calculator

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🔬 PCR Yield & Efficiency Calculator

N = N₀ × (1 + E)^n

Initial DNA copies (N₀) Number of Cycles (n) Efficiency (E) %

Hardy-Weinberg Equilibrium Calculator

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🧬 Hardy-Weinberg Equilibrium Calculator

Calculate expected genotype frequencies & χ² test

Observed Genotypes

AA (Homozygous Dominant) Aa (Heterozygous) aa (Homozygous Recessive)

Or Enter Allele Frequencies

p (Dominant allele frequency)

DNA/RNA Melting Temperature (Tm) Calculator

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🌡️ DNA/RNA Melting Temperature (Tm) Calculator

Calculate Tm for primers, probes & oligonucleotides

🔬 Sequence Input

Oligonucleotide Sequence (5' → 3')

Method Basic (Wallace Rule) - Fast & Simple Nearest-Neighbor (More Accurate)

Na⁺ Concentration (mM)

⚙️ Calculation Parameters

Primer Concentration (µM) DNA Type DNA RNA

Common Tm Guidelines:
• PCR Primers: 55–65°C
• Probes: 65–75°C
• Good Tm difference between forward & reverse primer: < 5°C

🌡️ Tm Calculation Results

Wallace Rule (Basic): Tm = 2°C × (A+T) + 4°C × (G+C)

Michaelis-Menten Enzyme Kinetics Analyzer

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⚡ Michaelis-Menten Enzyme Kinetics Analyzer

Calculate Vmax, Km & Analyze Enzyme Kinetics using Lineweaver-Burk Plot

📊 Enter Experimental Data

Add [S] (substrate concentration) and corresponding velocity (V)

📈 Enzyme Parameters

Enzyme Name (Optional)

Lineweaver-Burk Equation:
1/V = (Km / Vmax) × (1/[S]) + 1/Vmax

Add at least 4–5 data points for accurate linear regression.
Units: [S] in mM, V in µmol/min (common lab units)

📊 Analysis Results

Lineweaver-Burk Plot (1/V vs 1/[S])

Michaelis-Menten Kinetics • V = Vmax [S] / (Km + [S])