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;
17 Cards in this Set
- Front
- Back
Zebrafish: a model vertebrate (6 features)
|
Embryonic development external to female
Optical clarity Development of body plan complete at 24 hours High fecundity Short generation time Maintained at high density |
|
beta-galactosidase is encoded by which gene?
|
lacZ. Combined lacZ and neomycin is termed beta-geo
|
|
Cre is a
|
phage enzyme which which can excise segments of dna planked by loxP sites
|
|
ganciclovir
|
kills cells which have incorporated constructs expressing the thymidine kinase gene as thymidine kinase converts ganciclovir to a cytotoxic product.
|
|
luciferase is
|
an enzyme which converts luciferin to a phosphorescent product- allows measurement of expression with high sensitivity.
|
|
refractive index
|
velocity of light in a vacuum/ velocity of light in a given material
|
|
numerical aperture formula
|
NA=n sin u
n= the lowest refractive index between the obeject and first objective element u is 1/2 the angular aperture of the objective |
|
microscopy's three parts are
|
magnification, resolution, contrast
|
|
abbe's equation
|
dmin = 1.22λ / 2NA
|
|
Koehler
Illumination |
• Ensures illumination is centred
and even • Matches NA of condenser with objective to achieve maximal resolution • Improper set-up results in shadows, artefacts and incorrect colours. • Pre-requisite for contrastenhancing methods |
|
3 types of direct labelling
|
histological stains, ion indicators (live cell imaging), organelle labels (live cell imaging and fixed preparations).
|
|
3 types of antibody detection
|
horseradish peroxidase and DAB chromagen, fluorescent detection (alexa fluor/ FITC/ quantum dots) electron microscopy (nanogold labelling, DAB, quantum dots).
|
|
Multiple Testing =
|
when you are asking many questions at the same
time (e.g. studying many RNAs at once using a microarray). |
|
False Discovery Rate =
|
the number of incorrect findings you will
accept in your results (this is a common way of dealing with the problems raised by multiple testing) |
|
a gene regulatory network is...
|
a representation of relationships between RNAs
Proteins, signalling pathways and metaboiltes are the’ hidden engine’ that determines the gene network edges |
|
practical aspects of bioinformatics
|
evolutionary biology, structural bolecular modeling, phylogenetics, metagenomics
Genome sequencing, assembly, and mapping = generating and using information about genomes Genomic, Proteomic, Glycomic and Metabolomic analysis = gaining an understanding of biology and pathology by measuring the abundance of thousands of molecules in cells or tissues Integrative bioinformatics = Bringing data about different aspects of cells and tissues together to allow a more holistic understanding of normal function and pathology Clinical bioinformatics = bringing clinical information and molecular information together to optimise treatment |
|
Technical aspects of bioinformatics
|
Biological databases = large, organized bodies of persistent data,
usually associated with computerized software designed to mine the data Computational biology = the actual process of analyzing and interpreting biological data Bioinformatic tool development = the development of new algorithms (mathematical formulas) and statistics which assist interpretation of biological data In silico modeling = mathematic models of biological situations to limit the “search space” for laboratory hypotheses testing |