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1,000µL to mL
1mL
1mL to µL
1000µL
Molarity
The number of moles of solute per liter of solution
Formula for grams
Grams = Moles x Liters x Molecular weight
C1V1 = C2V2
Plug in your numbers, solve for the missing variable. Add V1 of stock, then add water up to the final volume V2, so the water is V2 - V1
Procedure when using a microcentrifuge
Make sure microcentrifuge tubes are balanced, if you have an uneven number of tubes, grab a blank (a microcentrifuge tube with something like water in it with the same volume) and add it to your missing spot.
Control variable
All the variables that might influence the dependent variable (e.g. reaction time)
Dependent variable
The aspect of the system that is showing response to the independent variable
Independent variable
The factor that is being tested in the current experiment
Research hypothesis
The opposite statement, the only way it can be supported is if there is experimental evidence to reject the null hypothesis (i.e. it can be falsified). For example: “Students who are not distracted will have different reaction time from distracted students.”
Null hypothesis
A statement of no difference. For example “Distracted and non-distracted students will have the same reaction time.”
Research Hypothesis
A statement that has a difference. For example: “Students who are not distracted will have different reaction time from distracted students.”
Interpret a p-value
The p-value is the evidence against a null hypothesis. The smaller the p-value, the stronger the evidence that you should reject the null hypothesis.
If p < 0.05
Reject the null and call it a significant difference
If p > 0.05
Fail to reject the null and call it no significant difference
Identify a proper negative control for an experimental setup
Water
Test that identifies simple sugars
Benedict’s test
Test that identifies starch
Lugol’s Reagent
Test that identifies lipids
Brown Bag/Paper Towel, Sudan IV
Test that identifies proteins
Biuret Test
How does Benedict’s test work
Causes a color change based on the percentage of sugar. It needs heat and goes blue to green to yellow to orange to brick red as sugar increases (reducing sugars reduce Cu²⁺)
How does Lugol’s Reagent work
Causes a color change based on if starch is present or not (Brown/Yellow = Negative, Blue/Purple = Positive)
How does the Brown Bag/Paper Towel Test work
Shows a grease spot if lipids are present and no spot if lipids are absent
How does Sudan IV work
It’s a lipid-soluble dye and shows darker red areas where it has stained lipids, if any
How does the Biuret test work
Shows a deep purple if proteins are present and a blue color if proteins are absent. Cu²⁺ binding peptide bonds in alkaline solution.
How does size exclusion chromatography work?
Larger molecules pass through, or are “excluded”, from the beads. As the liquid flows through the column, small molecules enter the beads and pass through the column more slowly.
Order of elution from a size exclusion chromatography column
The larger molecules pass quickly through the column and are collected in the initial set of tubes, and the smaller molecules end up in the later tubes.
How do you use a standard curve to calculate the molecular weight of an unknown protein
Find the unknown’s elution volume on the curve and read off its size.
Magnification
The extent to which an image is enlarged
Resolution
The distance between two objects that can be perceived
Microscope parts from the side

Microscope parts closer up

Scanning Electron Microscopy (SEM)
Uses a beam of electrons as a source of illumination. Electrons interact with the surface of the object, producing an image with a 3-D effect. The wavelength of the electron beam creates a resolution of ~0.4nm.
Maximum magnification of Scanning Electron Microscopy
~500,000x
How are specimens prepared for scanning electron microscopy
Coated with metal and imaged by electrons bouncing off the surface.
Transmission Electron Microscopy (TEM)
Uses a beam of electrons as a source of illumination. Electrons interact with the interior of the object. The wavelength of the electron beam creates a resolution of ~0.05nm.
Maximum magnification of Transmission Electron Microscopy
~1.000.000x
How are specimens prepared for Transmission Electron Microscopy
Uses ultra thin sections with heavy-metal stain and electrons passing through
Light Microscopy
Illumination: Visible light spectrum. Resolution ~0.2 micrometers. The unaided eye can resolve objects at ~0.2mm or ~200 micrometers.
Maximum magnification for Light microscopy
~1,000x
Eosin stain
Stains positively charged components of a cell (proteins located in the cytoplasm)
Methylene blue
Stains the nucleus (DNA located in the cell nucleus)
1mm to μm
1,000μm
1,000μm to nm
1,000,000nm
How alcohol size related to membrane damage
Longer alcohol chains increase membrane permeability
Relate absorbance values to membrane damage
The higher the absorbance value, the greater the membrane damage. Higher alcohol concentration also means more damage, and damaged membranes leak the beet pigment, which is why absorbance rises.
Instrumentation used to measure membrane damage
Colorimeter: measures the amount of light absorbed by a solution.