STAINING Flashcards

(67 cards)

1
Q

process of applying dyes on the sections to see and study the ______and physical characteristics of the cells.

A

STAINING ; architectural pattern of the tissue

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2
Q

is the primary diagnostic stain used in histology and histopathology.

A

H&E

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3
Q

This component stains cell nuclei blue/black with good intranuclear detail

A

HEMATOXYLIN

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4
Q

This component stains cell cytoplasm & most connective tissue fibers in varying shades & intensities of pink, orange & red.

A

EOSIN

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5
Q

BASIC DYE

A

HEMATOXYLIN

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6
Q

ACIDIC DYE

A

EOSIN

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7
Q

STAINS NUCLEUS

A

HEMATOXYLIN

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8
Q

STAINS CYTOPLASM AN EXTRACELLULAR FUBER

A

EOSIN

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9
Q

A natural substance which is obtained from the heartwood of the logwood tree

A

Hematoxylin campechianum.

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10
Q

The hematoxylin powder is crystallized out of solution. This powder is not readily ____

A

water soluble.

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11
Q

Hematoxylin does not contain _____(the part of the dye molecule essential for color) and would therefore be better described as potential dye rather than a true dye.

A

chromophore

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12
Q

active coloring agent is

A

hematin

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13
Q

oxidation of hematoxylin, a process known as___

A

ripening.

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14
Q

oxidizing hematoxylin (natural ripening) which may take as long as___

A

3-4 months.

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15
Q

most commonly used oxidizing agent.

A

SODIUM IODATE

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16
Q

The chemical oxidation converts the dye almost instantaneously but the product does not have ____

A

a shelf life.

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17
Q

Uses ___to demonstrate nuclear and cytoplasmic structures

A

mordants

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18
Q

Aluminum-salt lakes are usually

A

colored blue

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19
Q

ferric salt lakes are

A

colored blue-black.

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20
Q

A natural process wherein there is an exposure of the substance to air and sunlight for about 3-4 months.

A

NATURAL OXIDATION

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21
Q

To speed up the natural process of oxidation, we used sodium iodate or mercuric oxide.

A

CHEMICAL OXIDATION

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22
Q

NATURALLY RIPENED HEMATOXYLINS

A

Ehrich’s hematoxylin
Delafield’s hematoxylin

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23
Q

CHEMICALLY RIPENED HEMATOXYLIN

A

Sodium iodate in Mayer’s hematoxylin (SIM)
Mercuric chloride in Harris’ hematoxylin (MCh)

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24
Q

Hematin with mordant such as _____ forms a lake which functions as cationic dye and stains anionic tissue components.

A

ammonium or potassium alum

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25
Hematin in ___solution can be acidic or an alkaline dye depending on pH.
aqueous
26
An acidic dye that is negatively charged and stains basic structures in color red or pink
EOSIN
27
Commonly used as a background stain
EOSIN
28
A red acid dye with three forms:
YELLOWISH BLUISH ETHYL EOSIN
29
Process whereby tissue elements are stained in a definite sequence, and the staining solution is applied for specific periods of time until the desired intensity of coloring of the different tissue elements is attained.
PROGRESSIVE STAINING
30
With this technique, the tissue is first overstained to obliterate the cellular details.
REGRESSIVE STAINING
31
Is the microscopically controlled removal of stain from certain tissue components in order that specific tissue components are demonstrated.
DIFFERENTIATION (DECOLORIZATION)
32
A selective removal of stain - accomplished with the use of
acid alcohol, ethyl alcohol, diluent, or the mordant
33
After over-staining the section with alum hematoxylin, differentiation is carried out using ___
dilute HCl in 70% alcohol.
34
Process of restoring the hydroxyl ions loss during the process of acid differentiation (removes the lake giving the tissue a red color).
BLUEING
35
Most commonly used “blueing” agents
1% lithium carbonate dilute ammonium hydroxide Scott’s tap water substitute
36
Less commonly used are ___
potassium acetate sodium acetate 0.2%-0.5% bicarbonate solutions.
37
remove the wax from the section
Dewaxing/Deparaffinization
38
sections to water”
hydration
39
Haematoxylin solution (Harris or Mayer’s) minutes?
5 min
40
Differentiation Tap water 1% acid alcohol Tap water
- 6 dips - 5-10 min - 6 dips
41
a process where we stain a color of dye contrasting the principal stain, making the stain structure easily visible using a microscope or it used to color and contrast those colors that were retained during the first staining.
Counter (Cytoplasmic) Staining
42
Primary (nuclear) stain - Hematoxylin for __ Then counterstain - Eosin solution for ___
5 mins 3 mins.
43
Dehydration 95% alcohol 1 95% alcohol 2 100% alcohol 1 100% alcohol 2
all 1 min
44
Hydration process uses a ____concentration of alcohol while the dehydration process uses an____ concentration of alcohol.
descending . ascending
45
Calcium and calcified bone
Purplish blue
46
Cartilage matrix and mucin
May appear blue with some Alum hematoxylin stain
47
Karyosome
Dark purple
48
Erythrocytes
Deep pink; may have an orange hue due to their natural color
49
Collagen and osteoid tissue
light pink
50
3 major groups of staining
HISTOLOGICAL HISTOCHEMICSL IMMUNOHISTOCHEMICAL
51
METHODS OF STAINING
DIRECT' INDIRECT METALLIC IMPREGNATION VITAL STAINING INTRAVITAL SUPRAVITAL
52
Process whereby the tissue constituents are demonstrated in sections by direct interaction with a dye or staining solution, producing coloration of the active tissue component.
HISTOLOGICAL STAINING (MICROANATOMICAL STAINING)
53
Various constituents of tissues are studied through chemical reactions that will permit microscopic localization of a specific tissue substance.
HISTOCHEMICAL STAINING (HISTOCHEMISTRY
54
A combination of immunologic and histochemical techniques that allow phenotypic markers to be detected and demonstrated under the microscope, using a wide range of polyclonal or monoclonal fluorescent labeled or enzyme-labeled antibodies.
IMMUNOHISTOCHEMICAL STAINING
55
A combination of immunologic and histochemical techniques that allow phenotypic markers to be detected and demonstrated under the microscope, using a wide range of _____ OR ___
polyclonal or monoclonal fluorescent labeled or enzyme-labeled antibodies.
56
A process of giving color to the sections by using aqueous or alcoholic dye solution.
DIRECT
57
A process whereby the action of the dye is intensified by adding another agent; either mordant or accentuator.
INDIRECT
57
It merely accelerates or hastens the speed of the staining reaction by increasing the staining power and selectivity of the dye.
ACCENTUATOR
58
Is a process where specific tissue elements are demonstrated, not by stains, but by colorless solutions of metallic salts which are thereby reduced by the tissue, producing an opaque usually black deposit on the surface of the tissue or bacteria.
METALLIC IMPREGNATION
59
Most commonly used agent for impregnation which can also function as staining agent.
Gold (Gold Chloride) and Silver Nitrate
60
Is reduced by argentaffin cells (in melanin and intestinal glands) that form black deposits seen under the microscope.
Ammoniacal Silver
61
Selective staining of living cell constituents, demonstrating cytoplasmic structure by phagocytosis of the dye particle (cytoplasmic phagocytosis).
VITAL STAINING
62
Staining of living cells is done by injecting the dye into any part of the animal body (either intravenous, intraperitoneal or subcutaneous), producing specific coloration of certain cells, particularly those of the reticulo-endothelial system.
INTRAVITAL STAINING
63
Used to stain living cells immediately after removal from the living body.
SUPRAVITAL STAINING
64
Recommended for mitochondria = STAIN
JANUS GREEN
65
Why do we need to place the tissue slide in hot plate before staining?
Before staining, the tissue slides must be kept at 65 degrees Celsius on a hot plate for 20 minutes in order to remove all paraffin wax.
66
H&E PROCEDURE
DEWAXING HYDRATION PRIMARY STAINING DIFFERENTIATION BLUEING DISTILLED WATER COUNTER STAINING TEMPORARY MOUNTING DEHYDRATION CLEARING MOUNTING AND COVER SLIPPING EXAMINE