Staining is an auxiliary
techniqueused in microscopyto enhance contrast in the microscopic image.
biochemistryit involves adding a class-specific ( DNA, proteins, lipids, carbohydrates) dye to a substrate to qualify or quantify the presence of a specific compound. It is similar to fluorescent tagging.
dyes are frequently used in biologyand medicineto highlight structures in biological tissues for viewing, often with the aid of different microscopes. Stains may be used to define and examine bulk tissues (highlighting, for example, muscle fibers or connective tissue), cell populations (classifying different blood cells, for instance), or organelles within individual cells.
Biological staining is also used to mark cells in
flow cytometry, and to flag proteins or nucleic acids in gel electrophoresis.
Staining is not limited to biological materials, it can also be used to study the morphology of other materials for example the lamellar structures of semicrystalline polymers or the domain structures of block copolymers.
"In vitro" staining
In vitrostaining involves colouring cells or structures that are no longer living. Certain stains are often combined to reveal more details and features than a single stain alone. Combined with specific protocols for fixation and sample preparation, scientists and physicians can use these standard techniques as consistent, repeatable diagnostic tools. A counterstainis stain that makes cells or structures more visible, when not completely visible with the principal stain.
crystal violetstains only Gram-positivebacteria in Gram staining. A safranincounterstain is applied which stains all cells, allowing the identification of Gram-negative bacteria as well.
Methods of in vitro staining
The preparatory steps involved depend on the type of analysis planned; some or all of the following procedures may be required.
Permeabilization involves treatment of cells with (usually) a mild
surfactant. This treatment will dissolve the cell membranes, and allow larger dye molecules access to the cell's interior.
Fixation–which may itself consist of several steps–aims to preserve the shape of the cells or tissue involved as much as possible. Sometimes
heat fixationis used to kill, adhere, and alter the specimen so it will accept stains. Most chemical fixatives (chemicals causing fixation) generate chemical bonds between proteins and other substances within the sample, increasing their rigidity. Common fixatives include formaldehyde, ethanol, methanol, and/or picric acid. Pieces of tissue may be embedded in paraffinwax to increase their mechanical strength and stability and to make them easier to cut into thin slices.
Mounting usually involves attaching the samples to a glass microscope slide for observation and analysis. In some cases, cells may be grown directly on a slide. For samples of loose cells (as with a blood smear or a
pap smear) the sample can be directly applied to a slide. For larger pieces of tissue, thin sections (slices) are made using a microtome; these slices can then be mounted and inspected.
At its simplest, the actual staining process may involve immersing the sample (before or after fixation and mounting) in dye solution, followed by rinsing and observation.Many dyes, however, require the use of a
mordant: a chemical compound which reacts with the stain to form an insoluble, coloured precipitate. When excess dye solution is washed away, the mordanted stain remains.
A simple staining method for bacteria which is usually successful even when the "positive staining" methods detailed below fail, is to employ a
negative stain. This can be achieved simply by smearing the sample on to the slide, followed by an application of nigrosin(Indian ink). After drying, the microorganisms may be viewed in bright field microscopy as lighter inclusions well-contrasted against the dark environment surrounding them. Note: negative staining is a mild technique which may not destroy the microorganisms therefore it is unsuitable for studying pathogens.
Gram stainingis used to determine gram status to classify bacteria broadly. It is based on the composition of their cell wall. Gram staining uses crystal violet to stain cell walls, iodineas a mordant, and a fuchsinor safranincounterstain to mark all bacteria. Gram status is important in medicine; the presence or absence of a cell wall will change the bacterium's susceptibility to some antibiotics. Gram-positivebacteria stain dark blue or violet. Their cell wallis typically rich with peptidoglycanand lacks the secondary membrane and lipopolysaccharidelayer found in Gram-negative bacteria.
On most Gram-stained preparations,
Gram-negativeorganisms will appear red or pink because they are counterstained;due to presence of higher lipid content, after alcohol-treatment, the porosity of the cell wall increases & hence the CVI complex (Crystal violet -Iodine) can pass through. Thus, the primary stain is not retained. Also, in contrast to most Gram-positive bacteria, Gram-negative bacteria have only a few layers of peptidoglycan and a secondary cell membrane made primarily of lipopolysaccharide.
Ziehl-Neelsen staining is used to stain species of "
Mycobacterium tuberculosis" that do not stain with the standard laboratory staining procedures like Gram staining.
The stains used are the red colored
Carbol fuchsinthat stains the bacteria and a counter stain like Methylene blueor Malachite green.
•Haematoxylin and eosin (H&E) staining
Haematoxylin and eosin staining protocol is used frequently in histologyto examine thin sections of tissue. Haematoxylinstains cell nuclei blue, while eosinstains cytoplasm, connective tissue and other extracellular substances pink or red. Eosin is strongly absorbed by red blood cells, colouring them bright red.
Papanicolaou staining, or Pap staining, is a frequently used method for examining cell samples from various bodily secretions. It is frequently used to stain the Pap smearspecimens. It uses a combination of haematoxylin, Orange G, eosin Y, Light Green SF yellowish, and sometimes Bismarck Brown Y.
Periodic acid-Schiffstaining is used to mark carbohydrates ( glycogen, glycoprotein, proteoglycans). It is used to distinguish different types of glycogen storage diseases.
Masson's trichromeis (as the name implies) a three-colour staining protocol. The recipe has evolved from Masson's original technique for different specific applications, but all are well-suited to distinguish cells from surrounding connective tissue. Most recipes will produce red keratinand muscle fibers, blue or green staining of collagenand bone, light red or pink staining of cytoplasm, and black cell nuclei.
Romanowsky stains are all based on a combination of eosinate (chemically reduced eosin) and methylene blue(sometimes with its oxidation products azure Aand azure B). Common variants include Wright's stain, Jenner's stain, Leishman stainand Giemsa stain.
All are used to examine
bloodor bone marrowsamples. They are preferred over H&E for inspection of blood cells because different types of leukocytes (white blood cells) can be readily distinguished. All are also suited to examination of blood to detect blood-borne parasites like malaria.
Silver staining is the use of silverto stain histologic sections. This kind of staining is important especially to show proteins (for example type III collagen) and DNA. It is used to show both substances inside and outside cells. Silver staining is also used in temperature gradient gel electrophoresis.
Some cells are "argentaffin". These reduce silver solution to metallic silver after
formalinfixation. This method was discovered by Italian Camillo Golgi, by using a reaction between silver nitrateand potassium dichromate, thus precipitating silver chromate in some cells (see Golgi's method). Other cells are "argyrophilic". These reduce silver solution to metallic silver after being exposed to the stain that contains a reductant, for example hydroquinoneor formalin.
Sudan staining is the use of Sudan dyes to stain sudanophilic substances, usually lipids. Sudan III, Sudan IV, Oil Red O, and Sudan Black Bare often used. Sudan staining is often used to determine the level of fecal fatto diagnose steatorrhea.
Special technique designed for staining true endospores with the use of malachite green dye, once stained, they do not decolourize.
"In vivo" staining
"In vivo" staining is the process of dyeing living tissues—in "vivo" means "in life" (compare with "in vitro" staining). By causing certain cells or structures to take on contrasting color(s), their form (morphology) or position within a cell or tissue can be readily seen and studied. The usual purpose is to reveal cytological details that might otherwise not be apparent; however, staining can also reveal where certain chemicals or specific chemical reactions are taking place within cells or tissues.
Often these stains are called vital stains. They are introduced to the organism while the cells are still living. However, these stains are eventually toxic to the organism, some more so than others. To achieve desired effects, the stains are used in very dilute solutions ranging from 1:5,000 to 1:500,000 (Howey, 2000). Note that many stains may be used in both living and fixed cells.
Common biological stains
Different stains react or concentrate in different parts of a cell or tissue, and these properties are used to advantage to reveal specific parts or areas. Some of the most common biological stains are listed below. Unless otherwise marked, all of these dyes may be used with fixed cells and tissues; vital dyes (suitable for use with living organisms) are noted.
Acridine orange(AO) is a nucleic acid selective fluorescent cationic dye useful for cell cycle determination. It is cell-permeable, and interacts with DNA and RNA by intercalation or electrostatic attractions. When bound to DNA, it is very similar spectrally to fluorescein.
Bismarck brown(also Bismarck brown Y or Manchester brown) imparts a yellow colour to acid mucins. Bismarck brown may be used with live cells.
Carmineis an intensely red dye which may be used to stain glycogen, while Carmine alum is a nuclear stain. Carmine stains require the use of a mordant, usually aluminum.
Coomassie blue (also brilliant blue) nonspecifically stains proteins a strong blue colour. It is often used in gel electrophoresis.
Crystal violet, when combined with a suitable mordant, stains
cell walls purple. Crystal violet is an important component in Gram staining.
DAPIis a fluorescentnuclear stain, excited by ultravioletlight and showing strong blue fluorescence when bound to DNA. DAPI is not visible with regular transmission microscopy. It may be used in living or fixed cells.
Eosinis most often used as a counterstain to haematoxylin, imparting a pink or red colour to cytoplasmic material, cell membranes, and some extracellular structures. It also imparts a strong red colour to red blood cells. Eosin may also be used as a counterstain in some variants of Gram staining, and in many other protocols. There are actually two very closely related compounds commonly referred to as eosin. Most often used is eosin Y (also known as eosin Y ws or eosin yellowish); it has a very slightly yellowish cast. The other eosin compound is eosin B (eosin bluish or imperial red); it has a very faint bluish cast. The two dyes are interchangeable, and the use of one or the other is more a matter of preference and tradition.
Ethidium bromideintercalates and stains DNA, providing a fluorescent red-orange stain. Although it will not stain healthy cells, it can be used to identify cells that are in the final stages of apoptosis- such cells have much more permeable membranes. Consequently, ethidium bromide is often used as a marker for apoptosis in cells populations and to locate bands of DNA in gel electrophoresis. The stain may also be used in conjunction with acridine orange(AO) in viable cell counting. This EB/AO combined stain causes live cells to fluoresce green whilst apoptotic cells retain the distinctive red-orange fluorescence.
Fuchsinmay be used to stain collagen, smooth muscle, or mitochondria. Acid fuchsin is commonly used in Masson's trichrome and van Gieson's picro-fuchsin, and was used in an older method to stain mitochondria.
Haematoxylin(hematoxylin in North America) is a nuclear stain. Used with a mordant, haematoxylin stains nuclei blue-violet or brown. It is most often used with eosin in H&E (haematoxylin and eosin) staining—one of the most common procedures in histology.
Hoechst is a "bis"-benzimidazole derivative compound which binds to the "minor groove" of
DNA. Often used in fluorescence microscopy for DNA staining, Hoechst stains appear yellow when dissolved in aqueous solutions and emit blue light under UV excitation. There are two major types of Hoechst: "Hoechst 33258" and "Hoechst 33342". The two compounds are functionally similar, but with a little difference in structure. Hoechst 33258 contains a terminal hydroxylgroup and is thus more soluble in aqueous solution, however this characteristics reduces its ability to penetrate the plasma membrane. Hoechst 33342 contains a ethylsubstitution on the terminal hydroxyl group (i.e. an ethylether group) making it more hydrophobic for easier plasma membrane passage.
Iodineis used in chemistryas an indicator for starch. When starch is mixed with iodine in solution, an intensely dark blue color develops, representing a starch/iodine complex. Starch is a substance common to most plant cells and so a weak iodine solution will stain starch present in the cells. Iodine is one component in the staining technique known as Gram staining, used in microbiology.
Lugol's solution or Lugol's iodine (IKI) is a brown solution that turns black in the presence of starches and can be used as a cell stain, making the cell nuclei more visible.
Malachite green(also known as diamond green B or victoria green B) can be used as a blue-green counterstain to safranin in the Gimenez staining technique for bacteria. It also can be used to directly stain spores.
Methyl greenis chemically related to crystal violet, sporting an extra methyl or ethyl group.
Methylene blueis used to stain animal cells, such as human cheek cells, to make their nuclei more observable.
Neutral red(or toluylene red) stains nuclei red. It is usually used as a counterstain in combination with other dyes.
Nile blue(or Nile blue A) stains nuclei blue. It may be used with living cells.
Nile red(also known as Nile blue oxazone) is formed by boiling Nile blue with sulfuric acid. This produces a mix of Nile red and Nile blue. Nile red is a lipophilicstain; it will accumulate in lipidglobules inside cells, staining them red. Nile red can be used with living cells. It fluoresces strongly when partitioned into lipids, but practically not at all in aqueous solution.
•Osmium tetroxide (formal name: osmium tetraoxide)
Osmium tetraoxideis used in optical microscopy to stain lipids. It dissolves in fats, and is reduced by organic materials to elemental osmium, an easily visible black substance.
Rhodamineis a protein specific fluorescent stain commonly used in fluorescence microscopy.
Safranin(or Safranin O) is a nuclear stain. It produces red nuclei, and is used primarily as a counterstain. Safranin may also be used to give a yellow colour to collagen.
As in light microscopy, stains can be used to enhance contrast in
transmission electron microscopy. Electron-dense compounds of heavy metals are typically used.
phosphotungstic acidis a common negative stainfor viruses, nerves, polysaccharides, and other biological tissue materials.
Osmium tetraoxideis used in optical microscopy to stain lipids. It dissolves in fats, and is reduced by organic materials to elemental osmium, an easily visible black substance. Because it is a heavy metal that absorbs electrons, it is perhaps the most common stain used for morphology in biological electron microscopy. It is also used for the staining of various polymers for the study of their morphology by TEM. OsO4 is a very volatile. It is a strong oxidizing agent as the osmium has an oxidiztion number of +8. It aggressively oxidizes many materials, leaving behind a deposit of non-volatile osmium in a lower oxidation state
Ruthenium tetraoxideis equally volatile and even more aggressive than osmium tetraoxide and able to stain even materials that resist the osmium stain, e.g. polyethylene.
Other chemicals used in electron microscopy staining include:
ammonium molybdate, cadmium iodide, carbohydrazide, ferric chloride, hexamine, indium trichloride, lanthanum nitrate, lead acetate, lead citrate, lead(II) nitrate, periodic acid, phosphomolybdic acid, potassium ferricyanide, potassium ferrocyanide, ruthenium red, silver nitrate, silver proteinate, sodium chloroaurate, thallium nitrate, thiosemicarbazide, uranyl acetate, uranyl nitrate, and vanadyl sulfate. [http://www.2spi.com/catalog/chem/stain.shtml]
Cytology: the study of cells
Histology: the study of tissues
Immunohistochemistry: the use of antisera to label specific antigens
*Article categories for and
Ruthenium(II) tris(bathophenanthroline disulfonate), a protein dye.
*: category of articles on various dyes used for staining in microbiology and histology.
* [http://stainsfile.info/StainsFile/ StainsFile] reference for dyes and staining techniques
* [http://www.microscopy-uk.org.uk/mag/artfeb00/rhvital.html Vital Staining for Protozoa and Related Temporary Mounting Techniques] ~ Howey, 2000
* [http://www.microscopy-uk.net/mag/artoct00/fixation.html Speaking of Fixation: Part 1] and [http://www.microscopy-uk.net/mag/artdec00/fixation2.html Part 2] - by M. Halit Umar
* [http://www.histology-world.com/stains/stains.htm Photomicrographs of Histology Stains]
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