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Recombinant DNA
DNA produced by combining DNA from different sources
Plasmid
Small, circular piece of DNA located in the cytoplasm of many bacteria
Restriction Enzyme
Enzyme that cuts DNA at a specific sequence of nucleotides (molecular scissors)
DNA Ligase
Enzyme that chemically links DNA fragments together (molecular glue)
Polymerase Chain Reaction (PCR)
A technique used to make millions of copies of a specific DNA segment
Taq Polymerase
A heat-stable enzyme used in PCR to synthesize new DNA strands; it does not break down at high temperatures
Denaturation
The first step of PCR (95°C) where heat separates the double-stranded DNA
Annealing
The second step of PCR (~55°C) where primers attach to the target DNA sequences
Extension
The third step of PCR (72°C) where Taq polymerase adds nucleotides to build the new DNA strands
Gel Electrophoresis
A method used to separate DNA fragments based on their size and charge
DNA Charge
Negative (which is why it moves toward the positive/red electrode)
Micropipette
A tool used to measure and transfer very small volumes of liquid (measured in microliters)
Centrifuge
A machine that spins samples rapidly to separate substances by density (must be balanced)
Autoclave
A machine that uses high pressure and steam to sterilize equipment
Central Dogma
The directional flow of genetic information: DNA -> RNA -> Protein
Transcription
The process of copying a segment of DNA into mRNA (occurs in the nucleus)
Translation
The process of decoding mRNA to build a protein (occurs at the ribosome)
Heat Shock
The step in bacterial transformation (Ice -> 42°C -> Ice) that opens bacterial pores to let plasmids enter
Ampicillin
An antibiotic used in transformation labs to kill bacteria that did not take up the plasmid
Arabinose
The sugar added to nutrient plates to turn on (induce) the glowing GFP gene
Supernatant
The liquid lying above a solid residue after centrifugation
Pellet
The solid sediment at the bottom of a tube after centrifugatio