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definitions

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

restriction enzymes function

Back (Answer)

is a protein isolated from bacteria that splices DNA sequences at sequence-specific sites, creating DNA fragments with a known sequence at the end

#2
Front (Question)

where do restriction enzymes come from

Back (Answer)

naturally occurring in bacterium/being able to restrict viruses

#3
Front (Question)

what is a palindrome

Back (Answer)

same forwards and backwards on both strands of DNA

#4
Front (Question)

why is a palindrome important to restriction enzymes

Back (Answer)

allows enzyme to know where to cut, can recognize sequence on both strands, and insures that both strands are cut

#5
Front (Question)

what are sticky ends

Back (Answer)

when another type of restriction enzyme cuts a DNA sequence to create two uneven ends that connect back to one another easily (puts fragments together easy)

#6
Front (Question)

what are blunt ends

Back (Answer)

when a certain restriction enzyme separates a DNA sequence to create two ends of DNA which are equal on both sides (keeps fragments together)

#7
Front (Question)

DNA ligase function

Back (Answer)

attaches and rejoins DNA bases with complementary bases

#8
Front (Question)

recombinant DNA (DNA has been recombined)

Back (Answer)

fabricated by combining different parts of an organism into one (DNA that has been cut and pasted)

#9
Front (Question)

gel electrophoresis

Back (Answer)

separates large DNA fragments from small DNA fragments

#10
Front (Question)

why do DNA fragments travel through the gel

Back (Answer)

DNA is negative, when the machine is turned on the positive magnets pull the fragments through the gel

#11
Front (Question)

speed of small fragments

Back (Answer)

travel through gel faster because there is less of it

#12
Front (Question)

speed of large fragments

Back (Answer)

travel through gel slower because there is more of it

#13
Front (Question)

why do we have size standards

Back (Answer)

to compare the lengths of the fragments (measured in base pairs)

#14
Front (Question)

transforming bacteria

Back (Answer)

putting plasmid into bacteria

#15
Front (Question)

ways of transforming bacteria

Back (Answer)

shock, poison, cook

#16
Front (Question)

steps of cloning a gene

Back (Answer)

• cut plasmid and gene of interest • mix plasmid and gene of interest • dna ligase seals them • transform (shock, poison, cook) • it replicates during cell division

#17
Front (Question)

polymerase chain reaction

Back (Answer)

A PCR is a method that allows DNA copies to be made!! It uses a thermal cycler (PCR Machine)

#18
Front (Question)

why do we use PCR

Back (Answer)

allows us to create/duplicate DNA strands relatively easily compared to other methods.

#19
Front (Question)

steps of PCR

Back (Answer)

• heat: denature-creates two strands • build dna: annealing- primers add or “attach” a short piece of single stranded complementary DNA to both ends of the original DNA strand. • taq polymerase adds free floating nucleotides to each strand,

#20
Front (Question)

function of primers

Back (Answer)

they prepare or “prime” the site where taq polymerase can start working. This also ensures that either sides of the target region are copied on the Template DNA.

#21
Front (Question)

function of taq polymerase

Back (Answer)

adds free floating nucleotides to each strand

#22
Front (Question)

function of dna sequencing

Back (Answer)

tells us the sequence of the strands

#23
Front (Question)

genetic engineering

Back (Answer)

cutting and pasting dna

#24
Front (Question)

how can genetic engineering make GMO’s

Back (Answer)

-viral vectors -gene gun