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DNA charge
Negative → moves to positive electrode
Small DNA
Moves farther/faster
DNA ladder
Known sizes to compare
Restriction enzymes
Cut DNA at specific sites
See DNA
Stain + UV light
Spectrophotometer
Measures absorbance
Lambda max
Peak wavelength for your sample
Blank
Zero out with water/buffer
Standard curve
Match absorbance → concentration
More enzyme
Faster reaction
ONPG
Clear substrate → turns yellow when cleaved (cut)
Total magnification
Ocular × objective
Onion root tip
Meristem region = where cells divide
Interphase
Most cells here (not mitosis)
C₁V₁ = C₂V₂
Dilutions
M = moles / liters
Molarity
grams = M × L × MW
Making solutions
% = (grams / mL) × 100
Percent solutions