TEAS Science · Practice Question

    DNA Laboratory Techniques: TEAS Practice Question with Answer & Explanation

    An original TEAS 7-style science practice question, written for nursing-school applicants — with a full breakdown of every answer choice.

    Question

    A researcher has a sample containing DNA fragments of various lengths. Which laboratory technique should be used specifically to sort these segments based on their size/molecular weight?

    • A.Centrifugation
    • B.Chromatography
    • C.Gel Electrophoresis
      Correct
    • D.PCR (Polymerase Chain Reaction)

    Correct answer: C. Gel electrophoresis identifies DNA fragment size by using an electric field to pull negatively charged DNA through a porous gel.

    Understanding DNA Separation Techniques

    In molecular biology, scientists often need to visualize or isolate specific segments of DNA. Because DNA molecules all carry a negative charge but differ in length, we can use their physical properties to sort them.

    Why Gel Electrophoresis is the Correct Answer

    Gel Electrophoresis is the standard laboratory method used to separate macromolecules, such as DNA, RNA, or proteins, based on their size and electrical charge.

    • The Process: DNA samples are loaded into wells in a porous gel (usually agarose). An electric current is applied.
    • The Charge: Since DNA is negatively charged (due to its phosphate backbone), it migrates toward the positive electrode (anode).
    • The Sieve Effect: The gel acts like a molecular sieve or obstacle course. Smaller DNA fragments move through the pores easily and quickly, while larger fragments get tangled and move slowly. By the end of the run, the DNA is sorted into "bands" by size, with the smallest fragments furthest from the starting wells.

    Why Other Options Are Incorrect

    • A) Centrifugation: This technique spins samples at high speeds to separate components based on density. While it can separate DNA from cellular debris, it cannot sort different-sized DNA fragments into a measurable ladder or series of bands.
    • B) Chromatography: While chromatography separates mixtures (like pigments or proteins) based on chemical affinity or polarity, it is not the primary or most efficient tool for routine DNA size-sorting in a TEAS-level context.
    • D) PCR (Polymerase Chain Reaction): This is a common "trick" answer. PCR is used to amplify (make millions of copies of) a specific DNA sequence. While it creates the DNA segments, it does not separate them by size; you usually perform gel electrophoresis after PCR to see if your amplification worked.

    TEAS Concept: Molecular Biology Tools

    The TEAS exam expects you to know the basic purpose of common lab equipment. Remember that DNA is negative and "small runs fast."

    Study Tip: The "Obstacle Course" Analogy

    Think of gel electrophoresis as an obstacle course in a forest. Small children (short DNA fragments) can zip through the trees and bushes easily, while tall adults (long DNA fragments) get stuck on branches and move much slower. After 20 minutes, the kids will be much further along the path than the adults!

    Quick study tip: To remember the direction of DNA movement, remember 'Run to the Red'—DNA moves toward the positive (red) electrode because DNA is negative.

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