Here's an example of what's due today

SDS-PAGE gel results

Fri, Dec 11, 2026 · Week 16 · Genetics of Disease (Medical Interventions)

Today's goal: Read an SDS-PAGE gel to judge the size and purity of your isolated protein.

Learn first

What a finished product looks like

This is a model of the work you should turn in today. Use it to check your own: match the structure and the level of detail, do not copy it. Your data and wording should be your own.

Annotated SDS-PAGE gel reading
Completes: Completes the gel-interpretation task: an annotated SDS-PAGE reading with a labeled marker lane, estimated protein size, band counts by fraction, the most-pure fraction identified, and a QC statement.

How I read the gel: the marker (ladder) lane has bands of known molecular weights, so I use it as a ruler. Smaller proteins migrate farther down the gel, so I compare how far my band traveled to the marker to estimate size.

Reading:

  • My target band lines up near the 27 kDa marker band, so I estimate the protein is about 27 kDa.
  • Fraction 4 shows one strong band with almost no extra bands; fraction 2 shows several bands. So fraction 4 is the most pure.

QC statement: the purification met the purity goal, because the target fraction shows one dominant band at the expected size with very few contaminant bands, which is what a pure sample looks like.

LaneBands seenEstimated sizeNote
MarkerLadder of known sizesreferenceused as ruler
Fraction 2Several bandsmixedimpure, many contaminants
Fraction 4One dominant bandabout 27 kDamost pure, meets goal
Gel reading table: marker lane is the size ruler; fraction 2 has many bands (impure); fraction 4 has one dominant band at about 27 kDa (most pure).
Why this matters

This model shows the level of evidence and organization needed to complete: Completes the gel-interpretation task: an annotated SDS-PAGE reading with a labeled marker lane, estimated protein size, band counts by fraction, the most-pure fraction identified, and a QC statement.

Build yours step by step
  1. Name the variables and include units.
  2. Enter observations without changing the raw values.
  3. Check labels, calculations, and patterns before interpreting the data.
Change it for a new task

Keep the structure. Replace the question, facts, measurements, and evidence. Then recheck units, vocabulary, and whether the conclusion goes beyond the evidence.

Also due today: Attach your annotated gel reading to your Unit 4 PLTW tracker and submit it to Schoology.

Turn in: Annotated SDS-PAGE gel reading

Go to Schoology to turn this in.

Submit one PDF. Put your first and last name in the document header. Name the file: FirstName LastName - Assignment Title - YYYY-MM-DD.pdf.

Open Schoology PDF upload help

If you cannot get in, see Mr. Mendoza. Do not skip the work.

Claim ceiling: Today's evidence supports a classroom claim about SDS-PAGE gel results. It cannot prove causation, diagnose a real patient, or justify action outside this room.

Check yourself

WebXam problem for today's skill

One exam-style question that uses exactly what you practiced today. Try it before you reveal the answer, then read why each choice is right or wrong.

WebXam-style domain: Molecular and Genetic TechnologySelf-check skill: Judging protein purity from an SDS-PAGE band pattern
On an SDS-PAGE gel, fraction A shows one strong band at the expected molecular weight, while fraction B shows several bands of different sizes. Which fraction is more pure, and how can you tell?

Tap an answer to see the full explanation. Nothing is recorded or graded.

Why this practice matters

It builds this reusable test skill: Judging protein purity from an SDS-PAGE band pattern.

Use it on a new WebXam question
  1. Name the concept or data pattern being tested.
  2. Cross out choices that violate that rule or the evidence.
  3. Justify the best remaining choice before checking the answer.