Lab final Flashcards
(138 cards)
label the parts of the microscope
WORD BANK:
- arm
- base
- condenser
- coarse & fine focus knobs
- light intensity adjustment knobs
- light source
- objective lenses
- ocular lenses
- on/off switch
- slide movement
- stage
Handling a Microscope: DO
- Carry the scope with
two hands – one holding the arm, the other under the base - Start from the lowest magnification when observing slides
- Start with the stage all the way down, add the slide, make the stage go all the way up, focus down
- Set at lowest magnification before storing
Handling a Microscope: DO NOT
- Clean the lenses with anything but lens paper - Use the oil immersion lens without oil - Leave the light on or leave it on high intensity - Leave slides on the stage when you put the scope away - Pull the plug out from the cord
microscope magnifications
4x scanning: 40x
10x objective: 100x
40x objective: 400x
( x 10x eyepiece)
microscope resolution
- Resolution allows us to distinguish between two points or objects that are very close together
- not the same as magnification but is affected by the level of magnification used
- allows us to see objects as separate from one another
prokaryotes vs eukaryotes
- Presence/absence of nucleus and membrane-bound organelles
- Structure and location of DNA
- Cell wall structure/composition
- Differences in ribosomes, cytoplasm, flagella - Cell division and reproduction
- Size
types of prokaryotes
archaea and bacteria
prokaryotic archaea
now a separate kingdom; differences in genetic structure and metabolic pathways from other prokaryotes
prokaryotic bacteria
- remaining prokaryotes; you will be looking at:
a) Cyanobacteria – oxygenic photosynthetic bacteria with chlorophyll a
b) Gram positive & Gram negative bacteria
prokaryotes: cyanobacteria
- contain chlorophyll a, while other photosynthetic bacteria contain bacteriochlorophyll; important producers of oxygen!
- chlorophyll in thylakoid membranes within cytoplasm
- accessory pigments include carotenoids and phycobilins
- different forms: unicellular, colonial, filamentous
- many found in symbiotic relationships
bacterial shapes
- cocci: circular
- baccilus: rod shaped
- curved
- other
gram staining
1) application of crystal violet (purple dye)
2) application of iodine (mordant)
3) alcohol wash (decolorization)
4) application of safranin (counterstain)
* PURPLE = GRAM POSITIVE
* PINK = GRAM NEGATIVE
Seeds are alive but dormant until environmental conditions trigger __
germination
germination of seeds
When germination begins, seeds take up water, swell and split the seed coat. The young plant uses food stored in the seed to begin growth.
* process of using food involves RESPIRATION
respirometer
- Insert smaller
tube into larger tube, bottom of the smaller tube in your hand - Push the the smaller tube all the way to the end of the larger tube. You can use your pinky finger or a pencil (eraser end) or pen
- Keeping your finger (or pencil/ pen) in place, start to invert the tube
- Complete the inversion while keeping your finger (or pencil/ pen) in place
photosynthesis equation
6 CO2 + 6 H2O -> C6H12O6 (sugar) + 6 O2
psyn and light wavelength transmission
- The dye color is the light we see (reflected) and the light wavelength that is reaching the plant (transmitted)
- All other wavelengths are absorbed by the dye and are not available to the plant
micropipette use
- Twist dial to desired volume
- Pick up pipet tip
- Press plunger to first, soft stop
- Insert pipet tip into solution to be transferred
- Slowly release plunger to retrieve liquid
- Move pipet tip into desired tube
- Press plunger past first stop to second, hard stop to transfer liquid
DNA extraction- cheek cell prep
1) obtain hair follicle cells for DNA extraction OR rise mouth to obtain seek cells for DNA extraction
2) add sample to InstaGene matrix in micro test tube
3) incubate at 56ºC for 10 min, then vigorous agitation
4) incubate at 100ºC for 6 min, then repeat vigorous agitation
5) DNA template prep
what is needed for PCR?
- Template (the DNA you want to amplify for the study)
- Sequence-specific primers flanking the target sequence
- Nucleotides (dATP, dCTP, dGTP, dTTP)
- Magnesium ions (enzyme cofactor)
- Buffer, containing salt
- Taq polymerase
PCR reaction process
- DNA isolated from other cellular material
- DNA strands separated (“melted”) at high temperature
- primers bind to complementary sequences on the DNA strands
- Taq polymerase adds initial nucleotide to primer
- Taq polymerase extends and builds a complementary DNA sequence
how does PCR work?
- Heat (94°C) to denature DNA strands
- Cool (60°C) to anneal primers to template
- Warm (72°C) to activate Taq polymerase, which extends primers and replicates DNA
- Repeat multiple cycles
what does PCR stand for?
polymerase chain reaction
PV92 analysis
- Looking for the Alu sequence in the PV92 region of chromosome 16
- If lacking Alu, length is 641 base pairs (bp); if Alu is present, length is 941 bp
- Smaller particles migrate faster and farther through matrix than larger ones