Fri, Oct 2, 2026Fall (Semester 1) · Week 6Day 29 of 6780-min block

Aseptic technique

Today's target

Practice aseptic technique so you can grow a pure culture without contaminating it or yourself.

Due today · Pre-lab Required

Numbered aseptic technique procedure, contamination routes list, explanation of why plates are kept closed, safety rules for cultures and waste, and contamination prediction sketch.

Your 4 steps today
  1. 1
    Do this
    Practice aseptic technique so you can grow a pure culture without contaminating it or yourself.
  2. 2
  3. 3
    Submit this
    Pre-lab: Numbered aseptic technique procedure, contamination routes list, explanation of why plates are kept closed, safety rules for cultures and waste, and contamination prediction sketch.
  4. 4
    Submit it here
    1. 1CMSD website. Go to clevelandmetroschools.org and click the Clever button.
    2. 2Clever. Clever opens. Sign in if it asks.
    3. 3Microsoft (district) login. Use your district Microsoft account (the one for school).
    4. 4Schoology. Open Schoology, then your class, then Assignments, and find the file named below.
    The file to submit is named: Genetics of Disease (Medical Interventions) › Aseptic technique, culturing, selection, resistance genes, and data reliability. › Pre-lab
    Open Schoology
Were you absent? Jump to the make-up plan
Where this fits
Tested on (Ohio WebXam)
Genetics of Disease · 072130
PLTW lesson
MI · Aseptic technique
WebXam domain
Bio-Molecular Technology
Evidence to produce
Pre-lab
Lab / skill
CDC Antibiotic Resistance
Quick glossary
CER:
Claim, Evidence, Reasoning — make a claim, back it with evidence, explain your reasoning.
SOP:
Standard Operating Procedure — the exact steps to follow (especially in a lab).
Tracker:
Your PLTW progress log where you record completed evidence.
myPLTW:
The PLTW course site where you do the online activities — you open it through Schoology.
Learn first

Minute-by-minute · 80-minute block

💡 Big idea: How does a scientist prevent unwanted organisms from entering a culture and invalidating every result?

  1. 0-10 minBrainstorm and list every possible contamination route: air, hands, tools, talking, surfaces
  2. 10-25 minRead or watch the aseptic technique steps; write them in numbered order in your notebook
  3. 25-45 minDry practice: simulate flaming a loop (without flame), lifting a lid briefly with wrist only, working near the lab bench edge away from air currents
  4. 45-58 minExplain in writing why you minimize the time a plate is open; connect to the contamination routes listed earlier
  5. 58-68 minWrite one safety rule for handling bacterial cultures and one for disposing of used materials
  6. 68-80 minDraw and describe what a contaminated plate would look like versus a pure-culture plate
Mr. Mendoza's 5-minute intro
  • Aseptic technique is the single most important skill in microbiology; without it, every experiment is meaningless.
  • Hospitals use aseptic technique to prevent infections during surgery; you will use the same principles Wednesday in this lab.
  • Today you learn and practice the motions before any live cultures are involved.
  • Exit goal: a numbered aseptic technique checklist in your notebook and a dry run of every physical motion you will use tomorrow.
Do this, step by step
  1. 1List the ways a culture could get contaminated, from air to hands to tools.
  2. 2Watch or read the aseptic-technique steps and write them in order.
  3. 3Practice the motions dry: flaming a loop, lifting a lid briefly, working near the flame.
  4. 4Explain why you minimize the time a plate is open.
  5. 5Note one safety rule for handling cultures and waste.
  6. 6Predict what a contaminated plate would look like versus a clean one.
You'll be able to
  • You will be able to describe the steps of aseptic technique.
  • You will be able to explain how contamination happens and how to prevent it.
  • You will be able to handle cultures and waste safely.
Know by the end
  • Aseptic technique is a set of practices designed to prevent contamination of sterile materials and biological cultures.
  • Common contamination routes include: air currents, skin contact, talking or breathing near open plates, and unsterilized tools.
  • Contaminated plates grow mixed colonies that cannot be used to draw conclusions about a single bacterial strain.
📺 Tutor me: CDC: Healthcare-associated Infections (prevention basics)
Do the work

Your PLTW work today

Open this PLTW section today

Aseptic technique, culturing, selection, resistance genes, and data reliability. · Aseptic technique

Day 2 of this lesson. Open this exact section in myPLTW (reached through Schoology), then do the work below.

Do this: Open Activity 1.2.3 Attack of the Superbugs in myPLTW and review the culturing protocol before the lab.

Complete

Complete the pre-lab plan: aseptic technique steps, control wells labeled, and prediction of which antibiotic will produce the largest zone.

How far to get

Monday CER should be posted; pre-lab plan due today.

Upload as evidence

Pre-lab plan with aseptic steps and prediction in notebook.

All PLTW activities are completed inside the PLTW course environment — this page only gives direction. Submit producibles on Schoology.

The plan

Today's PLTW tracker

Check things off as you work, then submit. This tells Mr. Mendoza how you're doing so he can help the class. It does not replace turning in your producible on Schoology.

Use the code Mr. Mendoza gave you, not your name. Saved on this device.

Aseptic technique, culturing, selection, resistance genes, and data reliability.Day 2 of this projectSee the full week plan
Today's PLTW target

Aseptic technique, culturing, selection, resistance genes, and data reliability. · Aseptic technique

Open Activity 1.2.3 Attack of the Superbugs in myPLTW and review the culturing protocol before the lab.

Monday CER should be posted; pre-lab plan due today.

This is how Mr. Mendoza sees the class keeping pace with PLTW. Be honest, it only helps if it is accurate.

1 · What you do today

🎯 Practice aseptic technique so you can grow a pure culture without contaminating it or yourself.

  • List the ways a culture could get contaminated, from air to hands to tools.
  • Watch or read the aseptic-technique steps and write them in order.
  • Practice the motions dry: flaming a loop, lifting a lid briefly, working near the flame.
  • Explain why you minimize the time a plate is open.
  • Note one safety rule for handling cultures and waste.
  • Predict what a contaminated plate would look like versus a clean one.
2 · Turn in today

Pre-lab: Numbered aseptic technique procedure, contamination routes list, explanation of why plates are kept closed, safety rules for cultures and waste, and contamination prediction sketch.

Submit on Schoology

Upload by 11:29 PM for full credit.

3 · Who's doing what (team)
TaskWho
List the ways a culture could get contaminated, from air to hands to tools._______
Watch or read the aseptic-technique steps and write them in order._______
Practice the motions dry: flaming a loop, lifting a lid briefly, working near the flame._______
Explain why you minimize the time a plate is open._______
Note one safety rule for handling cultures and waste._______
Predict what a contaminated plate would look like versus a clean one._______

Working solo? Put your own name in "Who" for every row.

4 · Words I can use correctly
5 · I'm successful today when I can…
  • You will be able to describe the steps of aseptic technique.
  • You will be able to explain how contamination happens and how to prevent it.
  • You will be able to handle cultures and waste safely.
6 · Reflection & next steps
Where are you today?0/9 checked
Pick your period and code first.
Explore

Teacher-posted resources

Classroom documents for this lesson. Ones marked “Open the file” open right here; the rest are posted in Schoology. Use the label on each card to choose the right move.

Catch-up / reteachFor: Need extra support
PLTW-MI Daily Activity Tracker Unit 1 (Final)
worksheet/handoutOpens here
Open the file

Use this if you were absent, got stuck, or need another pass before you submit the lesson artifact.

Placement rationale

Matched Culturing, aseptic technique, superbugs by path:Medical-Interventions/Unit-1_How-to-Fight-Infection/00_Unit-Overview. Score 126. Visibility: student-schoology (student-facing resource; link through Schoology rather than local path).

Use during lessonFor: Everyone
MI Activity 1.2.1 Antibiotic Therapy
worksheet/handoutOpens here
Open the file

Open this when the class reaches this activity and use it to complete the required lesson artifact.

Placement rationale

Matched Culturing, aseptic technique, superbugs by path:Medical-Interventions/Unit-1_How-to-Fight-Infection/1.2_Antibiotic-Treatment. Score 126. Visibility: student-schoology (student-facing resource; link through Schoology rather than local path).

How to get there: open the CMSD website, click Clever, sign in with your Microsoft (district) account, then open Schoology from Clever.

Lab day

Lab & supplies

Bring / set up
Agar plates (or culturing simulation)Inoculating loopBunsen burner or sterile single-use loopsBacterial sample or brothIncubatorLabeling marker and tape
CDC Antibiotic Resistance
Words

This unit's vocabulary

aseptic techniqueculturecolonyinhibitionmutationhorizontal gene transfer

Tap the speaker to hear a term. Weekly vocabulary task: add two of these terms to your notebook glossary with a definition and an example in your own words.

Check yourself

WebXam practice

Tap an answer to check it · nothing is recorded or graded
What is the purpose of a four-quadrant streak plate when inoculating a bacterial culture?
On a transformation plate you see the expected white E. coli colonies plus several fuzzy gray-green colonies. What does this most likely indicate, and what should you do?
You inoculate selective LB-ampicillin broth with E. coli that you transformed with a plasmid carrying the ampicillin-resistance gene. What outcome do you expect after overnight growth at 37 degrees Celsius?
A single random mutation gives one bacterium a stronger cell wall that resists an antibiotic. How does this lead to a resistant infection?
Check yourself

Cumulative WebXam review

A quick mixed-review pulling questions from earlier units plus today, so the WebXam material stays fresh.

Tap an answer to check it · nothing is recorded or graded
[Review: Getting ready to test: serial dilutions and the ELISA setup] A technician makes a serial dilution starting with 100 ng/mL of antigen, transferring equal parts antigen and water at each step. What is the concentration after the first two dilutions?
[Review: Reading the color: running an ELISA and trusting your controls] An ELISA result is read simply as a color change with no number attached. This kind of observed, non-measurable result is called what?
[Review: How antibiotics fight bacteria and why resistance is rising] Which mechanism is the most common way bacteria share plasmids carrying antibiotic-resistance genes?
What is the purpose of a four-quadrant streak plate when inoculating a bacterial culture?
Explore

Where this leads — careers

What today's skills lead to. These are real health-science careers this course builds toward. Tap one to see, on the US Department of Labor's O*NET site, what the job actually involves, what it pays, and how fast it is growing.

Safety net

What to do if you were absent

If YOU are absent

Today is individual PLTW work, so do exactly what we did in class, from home: complete the same PLTW target above, then submit your Pre-lab.

Open Schoology (CMSD) and keep going

How to get there: open the CMSD website, click Clever, sign in with your Microsoft (district) account, then open Schoology from Clever.

If MR. MENDOZA is absent

Class still runs. Complete the online activity above (it's self-guided). Need the concept taught without a teacher? Use this authoritative explainer:

CDC Antibiotic Resistance
How this is graded
For: Pre-lab — Numbered aseptic technique procedure, contamination routes list, explanation of why plates are kept closed, safety rules for cultures and waste, and contamination prediction sketch.
  • Complete
    Every required part of the artifact is present, nothing left blank.
  • Accurate
    The science and the data are correct and match the evidence.
  • Scientific reasoning
    You explain your claim with evidence and reasoning (CER), not just an answer.
  • Professional communication
    Clear, organized, labeled, and written the way a clinician or scientist would.
  • Submitted
    Turned in the right way (Schoology for routine work) and confirmed.
Submission Zone

Drop your Fri, Oct 2, 2026 · Aseptic technique here. Use a clear file name (your initials + project). Routine work still goes to Schoology (via the CMSD portal).

Upload a project