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NanoDrop Spectrophotometer

Objective

Author(s): Matthew Chan, Ada Jiang

Quantify amount of extracted and purified plasmid DNA from bacterial cells using NanoDrop spectrophotometer.

Materials

Procedure

Protocol adapted from: NanoDrop 2000/2000c Spectrophotometer

DNA yield is determined by measuring the absorbance at 260 nm. The ratio of the readings at 260 nm and 280 nm. (A260/A280) provides an estimate of the purity of DNA with respect to UV absorbing contaminants such as protein.

Set-up Machine/Software
  1. start up and log into the computer.
    1. enter our username and password (on sticky note by our bench)

      usernameajiang
      passwordubcigem$2025
    2. log on to MI, click on nd-1000 v3.8.1 program

  2. in the nd-1000 v3.8.1 program, click User default > Nucleic acid > DNA-50
  3. clean pedestal with sterile water or dH2O
    1. load in 1 ul of water sample > click initialize
    2. load 1 ul of blank (liquid used to elute DNA), then click BLANK
Take measurements
  1. enter in sample ID

  2. take a reading of your plasmid using 1.0 μl of your plasmid DNA. Record the results in a table like so:

    Construct NameConcentration (ng/ul)A260/A280A260/A230
  3. exit and close program

  4. clean pedestal and gently lower the nanodrop arm onto clean folded kip wipe.

  5. log off > turn off computer