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Type A blood
A antigens present on the surface of red blood cells
B antibodies present in plasma
Can receive from type A or O
Can donate to type A and AB
Type B blood
B antigens present on the surface of red blood cells
A antibodies present in plasma
Can receive from type B or O
Can donate to type B or AB
Type AB blood
A & B antigens present on the surface of red blood cells
No antibodies present
Universal recipient
Can donate to type AB
Type O blood
No antigens present
A and B Antibodies present in plasma
Universal donor
Can receive from type O
Determining blood type
Clumping with Anti-A serum = A antigens present = type A blood
Clumping with Anti-B serum = B antigens = type B blood
Clumping with anti Rh factor = Rh factor present = positive
mitosis
duplication of a cell
growth and repair throughout body and life span
each new daughter cell = 46 chromosomes
meiosis
division (46 to 23 chromosomes)
produce gametes
homologous chromosomes separate
4 daughter cells with half the amount of chromosomes created
nondisjunction
occurs in either division of meiosis and with any 23 pairs of chromosomes
occurs only with meiosis
1st division: abnormal chromosomes → extra or missing
2nd division: both chromatids move into daughter cell
aneuploidy
missing or extra chromosome
very few seen in humans → most not comparable with human life
occurring on autosomes → more severe
on sex chromosomes → less severe
trisomy and monosomy
trisonomy → 3 copy of a particular chromosome, is survivable
monosomy → only one copy of a particular chromosome, lethal to fetuses
down syndrome
extra chromosome 21 (+21)
affects boys and girls equally
most frequently occurring chromosome disorder
short, heart defects, intellectual disability, suppressed immune system
genetic variation
diversity within a population occurring through crossing over, independent assortment, mutations, and reproduction
crossing over
“trading” of genes between homologous chromosomes
increase diversity among individuals within a population
via meiosis
independent assortment
chromosomes if each pair line up along equator at random
each pair of chromosomes line up along the equator indepedently if every other chromosome pair
mutations
changes in an individuals DNA
just happens or triggered by environment
natural selection
organisms within a species exhibit variation, some are more likely to survive in particular environments more than others
link to mutations: favorable traits are passed to offspring, resulting in a population mutating or changing over time
homologous chromosomes
two members if each chromosome pair
same length, banding, and genes for the same trait at the same location
autosomes
chromosome pairs 1-22
controls various characteristics throughout the body
chromosomes
46 individual chromosomes
23 pairs of chromosomes
homozygous
identical alles for a trait
AA, BB, bb, etc
heterozygous
two different alleles for a trait
sometimes only one allele is expressed
AO blood type, Bb, Aa, etc
dominant
allele that completely masks or hides the presence of the other allele
one copy dominant and one copy recessive → only dominant will be expressed
recessive
allele not expressed in presence if dominant allele
only will be expressed if no dominant allele is present
genotype
genetic makeup or type of genes an individual has for a particular trait
phenotype
ways in which genes are visibly expressed
X-linked recessive inheritance
a genetic pattern where a mutated gene on the X chromosome causes a condition, predominantly affecting males, due to males only possessing one X chromosome
if girl expresses an x-linked recessive trait, so does her father
for girls, mother must be either afflicted or a carrier and father must be afflicted to receive
X-linked dominant inheritance
if boy expresses a X-linked dominant trait, so does his mother
if a man expresses X-linked dominant trait, so does will all daughters
boys will only inherit from mothers
autosomal recessive inheritance
child can still express an autosomal receive trait even if neither parent expresses it (carriers)
two copies of recessive alleles
genetic mechanism where a trait or disorder manifests only when an individual inherits two mutated copies of a gene, one from each paren
autosomal dominant inheritance
needs only 1 copy of a dominant trait to express
child expresses an autosomal dominate trait, either one or both parents must also express the trait
a genetic pattern where a trait or disorder manifests if an individual inherits only one copy of a mutated gene from either parent
Purposes for DNA extracting
genetic testing
diagnose disease and disorders
identify human remains
analyze crime scene evidence
paternity testing
match organ donors and recipients
make copies of genes that are useful in producing antibodies
materials for dna extraction
blender separates cells from each other and break open surrounding cell walls
detergent breaks up phospholipids membranes around cell and nucleus and release dna
salt predicates dna out of solution so it is visible
meat tenderizer removes proteins allowing dna to operate and unwind
heat destroys or denature enzymes that break down dna and rupture membrane
ice bath slows breakdowns of dna while allowing cell membranes and protein to continue breaking down
filter paper traps proteins that have precipitated but allow dna to pass through
ethanol allows all components expect dna to mix
surface area:volume ratio
smaller = faster diffusion, bigger = slower diffusion
if ratio is smaller, cells can get oxygen and nutrients and excrete waste faster
dna replication
before cell divides, cell makes a copy of itself
double helix unwinds, unzipping down the middle, and new nucleotides pair up
nucleotide pairing
adenine and thymine
cytosine and guanine
genetic notation
indicates total number of chromosomes present, sex chromosomes, and abnormalities
order: number of chromosomes, sex chromosomes, and extra or missing chromosomes
sickle cell anemia
genetic disorder
must have 2 copies to have the disorder
causes body to make abnormal red blood cells “sickling” clogging bloodstream, blocking oxygen flow, and damage organs
% of identical DNA across species
99%
why dont single celled organisms grow larger
limitations in surface area:volume
as cells increase in size, its volume (needs) grows faster than surface area (supply), printing nutrient uptake