• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/39

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

39 Cards in this Set

  • Front
  • Back
How are restriction enzymes used?
They are used to cut DNA at a specific nucleotide sequence.
Where do restriction enzymes come from and how are they named?
They are found in bacteria and are named after the species in which the restriction enzyme was found.
Why are restriction enzymes used?
They are used by the gene for human insulin or human growth hormone by placing it into a bacterial plasmid.
How is a sticky end different then a blunt end?
A sticky end cut is used when one DNA fragment is combined with another DNA fragment to make a recombinant DNA. Blunt endcuts are used to isolate a fragment of DNA and to cut DNA into pieces for DNA fingerprinting.
What is a palindrome?
it is a sequence cut that has the same letters forward and backwards.
Why is DNA fingerprinting used?
To determine if there is a relationship between two people, to identify organisms causing a disease, and to solve crimes.
How does DNA fingerprinting work?
It is to evaluate the DNA in a person's cell.
What is Gel electrophoresis?
A mixture of DNA fragments that is placede at one end of a porous gel, and an electric voltage is applied to the gel.
What is the charge of DNA?
Negative
How does DNA travel differently from the dyes?
The DNA travels in the opposite direction of the dyes.
What is the function of the comb in DNA fingerprintype of the base thting?
To create wells in the gel.
What is the role of the buffer solution in DNA fingerprinting?
To force the gel into the wells.
How do fragments of various sizes travel through the gel?
The smaller the fragment the faster it travels.
What is the difference of the dideoxynucleotides?
It does not have an OH group at the 3' end, which prevents any nucleotides from binding to it. Also each of the four sequencing reactions has a different dideoxynucletide.
What is the role of the dideoxynucleotides?
Elongation of the strand continues until a dideoxynucleotide is reached. This causes fragments of various sizes or lengths to be produced.
How is the Sanger Method different from the method used today in sequencing labs?
Modern sequencing has all four bases in the same reaction tube. Each dideoxynucleotide has a fluorescent dye which is read by a laser using wavelengths which identifies the type of the base that ends the strands.
How many base pairs are in the human genome?
3 million base pairs.
How many genes are in the human genome?
Betwenn 20,000 and 25,000 genes.
What are some uses for the knowledge from the Human Genome Project?
Use of molecular medicine to improve the diagnosis of diseases. Use of microbial genomics research to create new energy sources. Reduce the likelihood of heritable mutations.
What is the purpose of PCR?
To analyze short sequences of DNA.
What is the first step of PCR?
1) [Denaturation at about 94 c] The double strand melts and seperates into single stranded DNA molecules.
What is the second step of PCR?
2) [Annealing at about 54 c] The primers bind to the single strand created in the previous PCR step.
What is the third step of PCR?
3) [Extension at about 72 c] The DNA polymerase adds nucleotides from 5' to 3', reading the template from 3' to 5' side, to make two double stranded molecules.
How does temperature change throughout the steps of PCR?
1) 94 celsius
2) 54 celsius
3) 72 celsius
What are primers and what are their roles (PCR)?
They are short single-stranded DNA sequences that are synthesized to correspond to the beginning and ending of the DNA stretch to be copied
What are other materials required to do the reaction (PCR)?
DNA molecule, 2 primers, and a polymerase enzyme.
Why is PCR commonly done before sequencing of DNA?
Because it gives you results much quicker and is usually essential.
What is Selective Breeding?
Allowing only those animals with a desired characteristics to produce the next generation.
What is Hybridization?
Crossing dissimilar individuals to bring together the best of both organisms.
What is Inbreeding?
The continued breeding of individuals with similar characteristics.
What is Genetic Engineering?
Making changes in the DNA code of a living organism.
What are Restriction Enzymes?
An enzyme that cuts DNA at a specific sequence of nucleotides.
What is Gel Electrophoresis?
A mixture of DNA fragments that is placed at one end of a porous gel, and an electric voltage is applied to the gel.
What is Recombinant DNA?
They are the DNA molecules that are reproduced by combining DNA from different sources.
What is the Polymerase Chain Reaction (PCR)?
A technique that allows biologists to make copies of a particular gene.
What is Plasmid?
A circular DNA molecule that is found naturally in some bacteria and is very useful for DNA transfer.
What is a Genetic Marker?
A gene that makes it possible to distinguish bacteria that carry the plasmid (and the foreign DNA) from those that don't.
What is Transgenic?
Organisms that contain genes from other species.
What is a Clone?
A member of a population of genetically identical cells produced from a single cell.