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01Microscopy
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snake-chicken-hydrogen-robert-friend-uranus
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Published
07/30/2024
a piece of glass/transparent material on which the material specimen is placed for examination under the microscope
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07/30/2024
a small, thin piece of glass used to cover the specimen on the microscope slide
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The Slide is {{c1::thicker::thickness}} than the coverslip
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technical term used by histologists to describe the microscopic appearance of cells and tissues after a histological section has been stained with a b…
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Basophilic cells and tissues are {{c1::acidic::pH}}
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attract basic dyes such as hematoxylin (H)
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Basophilic substances are dyed what color?
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a natural compound extracted from the heartwood ( dead, central wood ) of the logwood tree
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Hematoxylin is used for staining the {{c1::nucleus}}
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Hematoxylin acts as a {{c1::basic::pH}} dye
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Hematoxylin is {{c1::cationic::what ionic?}} ({{c1::positively}} charged) and reacts with {{c2::negatively}} charged nucleic acids in the nucleus
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{{c1::Eosinophilic}} - describes the appearance of cells and structures seen in histological sections which take up the staining dye eosin (E ) ; thes…
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{{c1::Eosinophils}} - attract {{c2::acidic::pH}} dyes such as eosin (E), and are dyed {{c2::red::color}}
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{{c1::Eosin (E)}} - a synthetic xanthene dye that stains the {{c2::extracellular matrix}} and{{c2::cytoplasm}} {{c3::pink}}an {{c4::acidic::pH}} dye t…
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Eosin is is {{c1::anionic}} ({{c1::negatively}} charged), thus it reacts with the {{c1::positively}} charged amino groups in proteins in the cytoplasm…
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Eosin shows the {{c1::general::general/specific}} layout and distribution of cells
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{{c1::Electron-dense}} - relatively impermeable to the electron beam of an electron microscope
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Electron-{{c1::dense::dense/lucent}} areas of the sample scatter electrons, leading to dark areas in the image or dark image
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{{c1::Electron-lucent}} - transparent to electrons , leading to a lighter image
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Electron microscopes {{c1::do NOT::do/do not}} need stains
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{{c1::Tissue section}} - tissues are cut into thin sections by a {{c2::microtome}}, then placed on a slide
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{{c1::Paraffin}} - {{c1::paraffin (wax)}} supports the tissue structure and enables very thin sections to be cut and mounted onto microscope slides fo…
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{{c1::Frozen}} - a pathological laboratory procedure to perform rapid microscopic analysis of a specimen (“cryosurgery”)
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{{c1::Resin}} - has numerous advantages over paraffin (improved morphology, lesser tissue shrinkage, thinner sections )
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1590: {{c1::Zacharias Janssen}} created the first optical telescope which uses lenses to see far away objects.
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{{c1::13th}} century: simple microscopes ( magnifying glasses/lens ) date back to the widespread use of lenses in eyeglasses that you have to hold.
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1610: {{c1::Galileo Galilei}} was cited as the compound microscope inventor.
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1625: {{c1::Giovanni Faber}} coined the name “microscope” for the one submitted by Galileo to the Accademia dei Lince.
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Italian scientist {{c1::Marcello Malpighi}} (Father of Histology) began his analysis of biological structure with the lungs .
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{{c1::Robert Hooke}} ’s Micrographia had a huge impact because of its impressive illustrations of what {{c1::Hooke}} saw. The first cells from an orga…
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{{c1::Antonie van Leeuwenhoek}} achieved up to 300 times magnification using a single lens or monocular microscope . He was called the “Father of Micr…
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1893: {{c1::August Kohler}} developed a key principle of sample illumination ({{c1::Kohler}} illumination) which is central to achieving or adjusting …
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1953: {{c1::Frits Zernike}} discovered phase contrast
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1955: {{c1::Georges Nomarski}} discovered differential interference contrast illumination
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{{c1::Microscope}}: an instrument used to see objects that are too small to be seen by the naked eye
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{{c1::Eyepiece Lens}} – the lenses at the top that you look through ; usually 10x (default) or 15x power, but can range from 5x to 30x
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{{c1::Tube}} – connects the eyepiece to the objective lenses
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{{c1::Head}} - Eyepiece + tube
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{{c1::Arm}} – supports the tube and connects it to the base ; where you hold the microscope
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{{c1::Base}} – the bottom of the microscope used for support
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{{c1::Illuminator}} – a steady light source up through the bottom of the stage; can be a mirror that focuses an external light source
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{{c1::Stage}} – the flat platform where you place your slides
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{{c1::Mechanical Stage}} – useful at higher magnifications (> 400x); enables you to move a slide easily over fractional distances where fingers are…
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{{c1::Stage Clips}} - holds the glass slides in place
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{{c1::Revolving Nosepiece or Turret}} – holds two or more objective lenses and can be rotated to easily change power
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{{c1::Objective Lenses}} – the lenses at the bottom near the stage; almost always consist of 4x, 10x, 40x, and 100x powers
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{{c1::Condenser}} - collects, focuses, and concentrates the light from the light source onto the specimen
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{{c1::Condenser Focus Knob}} - used to adjust the vertical height of the condenser to better focus the light
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{{c1::Iris Diaphragm}} - slit-like opening that controls the amount of light that reaches the specimen; situated within and works together with the co…
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{{c1::Coarse Adjustment Knob}} - moves the stage up and down to bring the specimen into focus. This knob produces large vertical movements of the stag…
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{{c1::Fine Adjustment Knob}} - used to bring the specimen into sharp focus under low power , and used for all focusing under high power
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{{c1::Light/Power Switch}} - turns the illuminator on/off
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The {{c1::optical microscope}} is also called {{c2::high power/biological}} microscope and also called a {{c2::compound lens}} microscope , because it…
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2nd set: objective lenses⇨ Scanning Objective/Scanner - {{c1::4}}x⇨ Low Power Objective (LPO) - {{c1::10}}x⇨ High Power Objective (HPO) - {{c1::40}}x⇨…
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Optical microscope resolution is limited to {{c1::0.25}} micrometers ; objectscloser than {{c1::0.25}} micrometers blur together
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Total magnification = ({{c1::eyepiece power}}) x ({{c1::objective lens power}})
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Electron microscopes can see resolution down to {{c1::0.2}} nanometers
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{{c1::SEM}} - produces 3D images of specimen’s surface only
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{{c1::TEM}} - produces 2D images of the plane section of the specimen
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{{c1::Scanning Probe Microscope}} - Generates a three-dimensional (3D) image of surfaces and structures of a nanoscale specimen, in the level of atoms…
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Specimen can be observed in real time with a {{c1::Scanning probe microscope}}
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Specimen is manipulated using an electric current with the physical probe tip in a {{c1::scanning probe micsoscope}}
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Look from the {{c1::side}} and turn the coarse adjustment knob to raise the stage
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After raising the stage to the closest position to the objective lens, look through the eyepiece and slowly turn the coarse adjustment knob in the {{c…
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{{c1::Stains}} - Used to enhance contrast in the specimen , therefore improving the viewing experience.
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{{c1::Hemotoxylin and Eosin}} is the most commonly used stain
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{{c1::Periodic Acid-Schiff (PAS)}} stains {{c2::complex carbohydrates}} a {{c3::magenta}} color
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{{c1::Masson trichrome}} stains {{c2::collagen}} {{c3::green or blue}}, {{c2::nuclei and cytoplasm}} {{c3::red}}, and {{c2::muscle}} {{c3::purple}}
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{{c1::Giemsa::stain}} is the standard stain for {{c2::blood cells}}
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{{c1::Basic::pH}} dyes are colored {{c2::cations(+)}} that bind to {{c2::anion(-)}} substrates (e.g. DNA)
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Eosin is {{c1::negatively}} charged
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{{c1::Lowest::Lowest/Highest}} molecular weight dye is added {{c2::first}} so it can penetrate the nuclear membrane and stain the nucleus, and is then…
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{{c1::Progressive}} staining is a type of staining process in which you add the dye and color builds up over time
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{{c1::Regressive staining}} - Type of staining process in which dye is added and overcolors everything. Successively, the excess is removed, which is …
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07/30/2024
Give an organelle that is basophilic.
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Last Update
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