TOPIC 6 Flashcards

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1
Q

normal body temperature

A

36.2 degrees celsius to 37.6 degrees celsuis

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2
Q

how long can temp. of body be used to estimate time of death

A

24hours

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3
Q

factors affecting rate of cooling (at least 4 marks)

A

body size, humidity, body position, surrounding temp. of environment , clothing

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4
Q

describe rigor mortis process

A
  • muscles starved of oxygen and reactions stop
  • respiration in cells becomes anaerobic and lactic acid produced
  • pH falls, inhibiting enzymes that stop anaerobic respiration
  • ATP no longer produced
  • bonds between muscle proteins fixed
  • muscles &joints fixed in place
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5
Q

give time length of rigor mortis

A
  • happens about 6-9 hours after death

- whole process wears off after 36 hours

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6
Q

autolysis

A

enzymes, in body from the digestive tract, and lysosomes break down cells

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7
Q
  1. process of body decompostion (6 marks)

think acronym and backstory

A

1.skin&lower abdomen turn green-sulhaemoglobin production(between 36&72 hours
after death)
2. body becomes reddish green then purplish black.
3. gas blisters appear on skin
4.body begins to smell and become bloated(due to gases e.g. CO2, CH4 etc) - 1
week after death
5. gas released and body deflates
6. fluid drains away and soft tissues shrink.

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8
Q
  1. forensic entomology-any details known to

help with generally graph questions

A

-succession of species of insect on body along with species present on body allows
stage of succession to be determined&time of death to be estimated

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9
Q

why is everyone’s DNA unique?

A

because of variety of sections of DNA not used to code for proteins (introns)

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10
Q
  1. exons
A

coding regions of DNA

EXPRESSED

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11
Q

introns

A

non-coding regions of DNA

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12
Q

Short Tandem Repeats (STRs)

A
  • short DNA sequences are repeated many times.
  • located within introns
  • sequence of repeated bases
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13
Q

why are STRs unique to each individual?

A

-number of times STRs are repeated on homologous chromosomes at a single locus
varies between individuals
ALTHOUGH … some STRs occur at the same place on both chromosomes of a
homologous pair

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14
Q

Steps of DNA Profiling (5 marks)

think acronym and backstory

A
  1. obtain tissue sample
  2. extract sufficient amount of DNA
  3. cut DNA into different sized fragments using RESTRICTION ENDONUCLEASES
    #only cut DNA at specific base sequences
  4. separate DNA fragments using gel electrophoresis
    5.compare sample with reference sample
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15
Q
  1. why do scientists use PCR?

POLYMERASE CHAIN REACTION

A

-samples obtained by forensics scientists at crime scene are too small to be
manipulated and experimented with.
- PCR amplifies tiny samples of DNA so they can be used in DNA profiling

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16
Q

what does PCR require

A
  • DNA Fragments
  • DNA polymerase
  • DNA Primers
  • Free Nucleotides
  • Thermocycler
17
Q

describe how small samples of dna can be

amplified

A

-PCR machine
-DNA polymerase enzyme added
-need for primers/ nucleotides
-heat to 95 degrees celsius, then cool down to 50 degrees celsius&then heat up
DNA to 70 degrees celsius
-cycle needs to be repeated several times to make several copied of DNA

18
Q

non overlapping genetic code

A

Each codon is non-overlapping

19
Q

codon.

A

The genetic code is formed from the
sequence of bases along the coding
strand of the DNA. We read the
genetic code as a series of three bases(CODON)

20
Q

degenerate nature of the

genetic code

A

Because there are 64 possible codons and only 20 amino acids quite
a few amino acids have more than one codon coding for them.
-MORE THAN 3 BASES CODE FOR ONE AMINO ACID

21
Q

. PCR Process (7 marks)

A

Polymerase Chain Reaction:
1. Heat sample of DNA to 95°C - H bonds break & it becomes
single-stranded.
2. Add free nucleotides - they will H bond with complimentary
partners in DNA
3. Add RNA Primers - short lengths of single-stranded RNA
that bind to the DNA and stop it annealing
4. Cool to 37°C - allows H bonds to form between nucleotides
5. Add DNA Polymerase
6. Heat to 72°C - optimum temp for thermophilic bacterium (not denatured at
high temp.)
7.REPEAT 20-30 TIMES TO FORM CYCLES

22
Q

steps in DNA fingerprinting technique?

A

obtain DNA sample
-amplify DNA sample using PCR
-cut DNA into fragments using restriction endonucleases
-dna fragments separated by gel electrophoresis according to their size
-dna placed on agarose gel, which is submerged in a buffer solution and
connected to electrodes
-dna current applied
-southern blotting used
-dna radioactive probe added to membrane
-x ray film placed next to membrane
-x ray film developed

23
Q

features of bacteria DEFFO

A

ribsosomes (70s)
circular DNA
plasmids
cytoplasm

24
Q

Ribosomes -bacteria

A

Same function as eukaryotic cells ( site of protein synthesis),
but are smaller (70s rather than 80s)