1/21
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
How should you check the inoculating tool is cool enough to collect a sample?
by lightly touching it to an uninoculated area on the agar plate
Which pipette would you use to measure/collect less than or equal to 1mL?ย
micropipetter
Which pipette would you use to collect/measure volumes between 1mL - 50mL/
serological pipettes
How should you hold your pipette?
keep it straight up always
A micropipetter that is labeled with p200 or 20/200 has a max volume of ______?
200 uL
For a micropipetter you use the units ______ and for serological pipette your use the units ______ .
uL and ml
1000ul is equal to ___________ mL.
1
1mL of water is equal to _____ g
1
What type of paper should you use to clean the lens of the microscope?
lens paper
When do you need to use the immersion oil?
100x objective
How many streaks/quadrants should you have when completing a Streak for Isolation?
4
order of reagants for gram stain
crystal violet
iodine
decolorizing agent
safranin
A gram-negative culture will appear _________ when Gram-stained.
pink
A gram-positive culture will appear __________ when Gram-stained.
purple
All differential staining procedures have _________ key steps.
3
How do you prepare a smear?
Draw a circle on slide, Add bacterial sample using inoculating tool or pipette inside circle, wait for sample to dry
Cells that have thin peptidoglycan layers will be Gram-________________.
negative
Cells that have a thick peptidoglycan layer will be Gram-____________.
positive
How long must you wash your stain with acid alcohol?
10-15 seconds
Which stop must you go to when collecting samples?
first stop
What stop must you to release the sample?
second stop
The ability of lenses to show two adjacent objects a discrete entities is referred to as
resolution