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Cresyl violet acetate

Cresyl violet acetate is a fluorescent stain used in histology and microscopy to visualize Nissl substances in neuronal cell bodies.
It is a cationic dye that binds to negatively charged molecules, particularly ribonucleic acids, allowing for the identification of rough endoplasmic reticulum and ribosomes within neurons.
This stain is commonly used in neuroanatomical studies to analyze the morphology and distribution of various neuronal populations.
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Most cited protocols related to «Cresyl violet acetate»

The cytoarchitecture of the PFC was studied in ten adult, male mice (strain C57BL/6) of similar weight (approximately 20 g). These control mouse brains were kindly donated and immersion fixed by Dr. H. Manji, NIMH, USA. All animal procedures were in strict accordance with the NIH animal care guidelines. The histological processing of these brains was performed at the laboratory of Dr. Rajkowska. The brains were embedded in 12% celloidin, cut into 40-μm serial sections using a sliding microtome and Nissl (1% cresyl violet) stained. Celloidin was chosen as an embedding medium to allow for the preparation of ‘thick’ sections with clear morphology and high contrast of Nissl-stained neurons and glial cells. In these immersion-fixed brains, any spots showing pycnotic reaction were not incorporated in this study.
In addition to these ten mice, four adult male mice (C57BL/6 strain) were stained for dopamine and four adult male mice for AChE, myelin, and immunohistochemically for SMI, PV and CB. For each staining, a different set of sections with several consecutive sections stained with Nissl at HBMU’s laboratory was used. The antibodies applied were the dopamine (DA) antibody (Geffard et al. 1984 (link)), SMI-32 antibody (Sternberger Monoclonals Inc., Baltimore, MD, USA: monoclonal antibody to one epitope of non-phosphorylated tau neurofilaments, lot number 11), SMI-311antibody (pan-neuronal neurofilament marker cocktail of several monoclonal antibodies for several epitopes of non-phosphorylated tau protein, Sternberger Monoclonals Inc., Baltimore, MD, USA: lot number 9) (SMI antibodies are presently distributed through Covance Research Products, USA), monoclonal anti-CB D-28K antibody (Sigma, St. Louis, MO, USA: product number C-9848, clone number CB-955, lot number 015K4826), and monoclonal anti-PV antibody (Sigma, St. Louis, MO, USA: product number P-3171, clone number PA-235, lot number 026H4824). Mice to be stained for DA were intracardially perfused under deep pentobarbital anesthesia (1 ml/kg body weight, i.p.), with saline followed by fixative. For DA staining, the fixative was 5% glutaraldehyde in 0.05 M acetate buffer at pH 4.0. After perfusion, the brains were immersed in 0.05 Tris containing 1% sodium disulfite (Na2S2O5) at pH 7.2 (De Brabander et al. 1992 (link)). Mouse PFC was sectioned at 40 μm by a vibratome. These sections were stained overnight in a cold room at 4°C using the polyclonal primary antibody sensitive to DA that was raised in the Netherlands Institute for Brain Research (NIBR) (Geffard et al. 1984 (link)), the specificity of which had been demonstrated previously (Kalsbeek et al. 1990 (link)). DA antiserum was diluted 1:2,000 in 0.05 M Tris containing 1% Na2S2O5 and 0.5% Triton X-100, pH 7.2. After overnight incubation, the sections were washed three times with Tris-buffered saline (TBS) and subsequently incubated in the secondary antibody goat–antirabbit, also raised in NIBR at 1:100 for 1 h. After having been rinsed 3× in TBS, it was incubated in the tertiary antibody, peroxidase–antiperoxidase, at 1:1,000 for 60 min. Both the secondary and the tertiary antibodies were diluted in TBS with 0.5% gelatine and 0.5% Triton X-100. For visualization, the sections were transferred into 0.05% diaminobenzidine (DAB; Sigma) with 0.5% nickel ammonium sulfate. The reaction was stopped after a few minutes by transferring the sections to TBS (3 × 10 min), then the sections were mounted on slides, air dried, washed, dehydrated and coverslipped.
Mice to be stained with anti-PV, anti-CB and SMI-32 and SMI-311 were fixed with 4% formaldehyde solution in 0.1 M phosphate buffer at pH 7.6. Mouse PFC was sectioned at 40 μm by a vibratome. To prevent endogenous peroxidase activity, free-floating sections were pretreated for 30 min in a Tris-buffered saline (TBS) solution containing 3% hydrogen peroxide and 0.2% Triton X-100. To prevent non-specific antibody staining, these sections were placed in a milk solution (TBS containing 5% nonfat dry milk and 0.2% Triton X-100) for 1 h. Incubation of the primary antibody, directly after the milk step was carried out overnight in a cold room at 4°C. The primary antibodies were diluted in the above-mentioned milk solution: SMI-32 and SMI-311 at 1:1,000, PV antibody at 1:1,000, and CB antibody at 1:250. For the monoclonal SMI-32, SMI-311, PV and CB antibodies, raised in mice, we used peroxidase-conjugated rabbit–antimouse (1:100 in 5% milk solution with 0.2% Triton X-100) as a secondary antibody. Visualization took place in 0.05% diaminobenzidine enhanced with 0.2% nickel ammonium sulfate. The reaction was stopped after a few minutes by transferring these sections to TBS (3 × 10 min), after which the sections were rinsed in distilled water, mounted on slides, air dried, washed, dehydrated and coverslipped. Control sections that were incubated according to the same procedure as described above, omitting the primary antibody, were all negative. All sections were cut coronally, because the coronal plane offers in general the best view to differentiate between the subareas of the rodent PFC (Uylings et al. 2003 (link); Van de Werd and Uylings 2008 (link)).
Sections were processed for AChE staining according to the protocol described by Cavada et al. (1995 (link)). The sections were incubated overnight in a solution of cupric sulfate and acetate buffer at pH 5 to which acetylthiocholine iodide and ethopropazine were added just before the start of incubation. After rinsing, the sections were developed in a sodium sulfide solution until a light brown color appeared and subsequently intensified to a dark brown color in a silver nitrate solution. Finally, the sections were differentiated after rinsing in a thiosulfate solution, dehydrated and mounted. In all steps, the solutions and sections were shaken constantly. The myelin was stained with silver by physical development according to Gallyas (1979 (link)). The sections were first placed in 100% ethanol and then immersed in a 2:1 solution of pyridine and acetic acid for 30 min. After rinsing, they were placed in an ammonium silver nitrate solution and after rinsing with 0.5% acetic acid, the sections were immersed in the optimal physical developer solution at room temperature (Gallyas 1979 (link)) until they showed good stain intensity under the microscope. Then the development of the staining was stopped in 0.5% acetic acid and the sections were dehydrated and mounted with Histomount. The sections were studied at intervals of 80–160 μm, and examined under a light microscope at a 63× magnification.
Publication 2010
For optic nerve crush surgery, mice were anesthetized with ketamine (6 mg/mL) and xylazine (0.4 mg/mL). The crush protocol was performed as described previously [26 (link)] using an intraorbital approach. Only the left eye of each mouse underwent the procedure. The loss of ganglion cells is a continuous process over a 3–4 week period, therefore we examined the time point at which there was the earliest maximum difference between the resistant and susceptible strains. Both DBA/2J and BALB/cByJ mice exhibit minimal cell loss at one week, followed by a period of rapid cell loss between 1 and 2 weeks. Each strain also exhibits modest cell loss after this point, but the difference between the two is not different than that observed at 2 weeks after crush (data not shown). For this reason, we examined all populations of mice at 2 weeks after optic nerve crush.
To quantify cell loss, mice were euthanized and the superior region of each eye was marked with an ophthalmic cautery prior to enucleation. Each eye was then enucleated and fixed for 1 h at 22°C in 4% paraformaldehyde in 0.1 M phosphate buffer (pH 7.4) containing 100 mM NaCl (PBS) followed by rinsing in PBS. An eyecup of the posterior pole was isolated and incubated in PBS containing 0.3% TritonX-100 (v/v), overnight at 22°C. Following incubation, the retina was dissected and mounted (ganglion cell layer up) on a glass "Plus" slide (Fisher Scientific, Chicago, IL), dried, and flattened under a coverslip weighted with a 10 g weight [66 ]. Dry retinas were stained by painting them with 1% cresyl violet acetate in 0.25% acetic acid [67 ]. Stained retinas were then differentiated and dehydrated in 100% ethanol, cleared in xylene, and coverslipped. Each slide contained the control and experimental retinas from a single mouse.
For counting cells in the ganglion cell layer, we captured digital images taken at 200× magnification using an Olympus BX40 light microscope (Olympus, Mellville, NY) with a SONY DXC-390 video camera attachment (Sony, New York, NY) and imported them into Image Pro Plus v4.5 (Media Cybernetics, Inc., Silver Springs, MD) quantification software. Parameters were set to automatically identify cells with round nuclei greater than 4 μm in diameter and exclude vascular endothelial cells (with spindle-shaped nuclei) and small densely staining cells that are common in the mouse retina [68 (link)]. The selection process did not distinguish between ganglion cells and large amacrine cells, but previous studies have estimated the proportion of ganglion cells in this layer to be 40–60% of the neurons present [26 (link),68 (link),69 (link)]. The number of cells present in a minimum of 4 microscopic fields, each encompassing an area of 0.33 mm2 and taken in the peripheral to midperipheral region around the 4 quadrants of each retina, was counted. In non-experimental retinas, the total numbers of cells ranged from 2055 – 2913 per field, consistent with previous reports of neuronal cell density in this layer [69 (link)]. The numbers of cells present in each retina was taken as the average of these counts and cell loss was calculated in each mouse as the percent change between the control and experimental eyes. Overall, we counted approximately 10% of the neurons present in each retina, which previous studies have demonstrated provides an accurate estimate of the loss of retinal ganglion cells after optic nerve crush [25 (link),26 (link),48 (link)].
Ganglion cell number was also estimated in untreated eyes of DBA/2J and BALB/cByJ mice by axon counting. Briefly, the optic nerves of 5 eyes from each strain were harvested and fixed overnight in 2.5% glutaraldehyde in PBS and then embedded in glycol methacrylate (JB-4 Plus, PolyScience, Worthington, PA). Transverse sections of 2 μm thick were cut approximately 1 mm from the globe and stained by silver impregnation to identify axons [67 ]. Axon counting was conducted as described previously [36 (link)] using 3 sections from each nerve.
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Publication 2007
The cytoarchitecture of the prefrontal cortex was studied in ten adult, male mice (strain C57BL/6) of similar weight (approximately 20g). These control mouse brains were kindly donated and immersed fixed by Dr. H. Manji, NIMH, USA. All animal procedures were in a strict accordance with the NIH animal care guidelines. The histological processing of these brains was performed at the laboratory of Dr. Rajkowska. The brains were embedded in 12% celloidin, cut into 40μm serial sections using a sliding microtome and Nissl (1% cresyl violet) stained. Celloidin was chosen as an embedding medium to allow for the preparation of ‘thick’ sections with clear morphology and high contrast of Nissl stained neurons and glial cells. In these immersion-fixed brains, any spots showing pycnotic reaction were not incorporated in this study.
In addition to these ten mice, four adult male mice (C57BL/6 strain) have been stained for dopamine and four adult male mice for acetylcholinesterase (AChE), myelin, and immunohistochemically for SMI, parvalbumin and calbindin: per staining a different set of sections with several consecutive sections stained with Nissl at HBMU's laboratory. The antibodies applied are the dopamine (DA) antibody (Geffard et al., 1984 (link)), SMI-32 antibody (Sternberger Monoclonals Inc., Baltimore, MD, USA: monoclonal antibody to one epitope of non-phosphorylated tau neurofilaments, Lot Number: 11), SMI-311antibody (Pan-Neuronal Neurofilament Marker cocktail of several monoclonal antibodies for several epitopes of non-phosphorylated tau protein, Sternberger Monoclonals Inc., Baltimore, MD, USA: Lot Number 9) [SMI antibodies are presently distributed through Covance Research Products, USA], monoclonal anticalbindin D-28K antibody (Sigma, St. Louis, Mo., USA: Product Number: C-9848, Clone Number: CB-955, Lot Number: 015K4826), and monoclonal anti-parvalbumin antibody (Sigma, St. Louis, Mo., USA: Product Number: P-3171, Clone Number: PA-235, Lot Number: 026H4824). Mice to be stained for DA were intracardially perfused under deep pentobarbital anaesthesia (1 ml/kg body weight, i.p.), with saline followed by fixative. For DA staining the fixative was 5% glutaraldehyde in 0.05 M acetate buffer at pH 4.0. After perfusion the brains were immersed in 0.05 Tris containing 1% Sodium disulfite (Na2S2O5) at pH 7.2 (De Brabander et al. 1992 (link)). Mouse prefrontal cortex was sectioned at 40 μm by a vibratome. These sections were stained overnight in a cold room at 4° C. using the polyclonal primary antibody sensitive for DA raised in the Netherlands Institute for Brain Research (NIBR) (Geffard et al. 1984 (link)) of which the specificity has been demonstrated previously (Kalsbeek et al. 1990 (link)). DA antiserum was diluted 1:2,000 in 0.05 M Tris containing 1% Na2S2O5 and 0.5% Triton X-100, pH 7.2. After overnight incubation the sections were washed three times with Tris buffered saline (TBS) and subsequently incubated in the secondary antibody goat-antirabbit, also raised in NIBR, at 1:100 for 1 h. and, after having been rinsed 3x in TBS, incubated in the tertiary antibody, peroxidase-antiperoxidase, at 1:1,000 for 60 min. Both the secondary and the tertiary antibodies were diluted in TBS with 0.5% gelatine and 0.5% Triton X-100. For visualization the sections were transferred into 0.05% diaminobenzidine 9(DAB; Sigma) with 0.5% nickel ammonium sulphate. The reaction was stopped after a few minutes by transferring the sections to TBS (3x 10 min), then the sections were mounted on slides, air dried, washed, dehydrated and coverslipped. Mice to be stained with antiparvalbumin, anticalbindin and SMI-32 and SMI-311 were fixed with 4% formaldehyde solution in 0.1 M phosphate buffer at pH 7.6. Mouse prefrontal cortex was sectioned at 40 μm by a vibratome. To prevent endogenous peroxidase activity free-floating sections were pretreated for 30 min in a Tris-buffered saline (TBS) solution containing 3% hydrogen peroxide and 0.2% Triton X-100. To prevent non-specific antibody staining, these sections were placed in a milk solution (TBS containing 5% nonfat dry milk and 0.2% Triton X-100) for 1 h. Incubation of the primary antibody, directly after the milk step, was carried out overnight in a cold room at 4%. The primary antibodies were diluted in above-mentioned milk solution: SMI-32 and SMI-311 at 1:1,000, parvalbumin antibody at 1:1,000, and calbindin antibody at 1:250. For the monoclonal SMI-32, SMI-311, parvalbumin and calbindin antibodies, raised in mice, we used peroxidase-conjugated rabbit-antimouse (1:100 in 5% milk solution with 0.2% Triton X-100) as a secondary antibody. Visualization took place in 0.05% diaminobenzidine enhanced with 0.2% nickel ammonium sulphate. The reaction was stopped after a few minutes by transferring these sections to TBS (3x 10 min), after which the sections were rinsed in distilled water, mounted on slides, air dried, washed, dehydrated and coverslipped. Control sections incubated according to the same procedure as described above, but omitting the primary antibody were all negative. All sections have been cut coronally, because the coronal plane offers in general the best view to differentiate between the subareas of the rodent prefrontal cortex (Uylings et al. 2003 (link); Van de Werd and Uylings 2008 (link)).
The sections were studied at intervals of 80-160 μm, and were examined under the light-microscope at a 63x magnification.
Sections have been processed for acetylcholinesterase staining according to protocol described by Cavada et al. (1995) (link). The sections were incubated overnight in a solution of cupric sulphate and acetate buffer at pH 5 to which acetylthiocholine iodide and ethopropazine were added just before the start of the incubation. After rinsing the sections were developed in a sodium sulphide solution until a light brown color appeared and subsequently intensified in a silver nitrate solution until a dark brown color. Finally, the sections are differentiated after rinsing in a thiosulphate solution, dehydrated and mounted. In all steps the solutions and sections were shaken constantly. The myelin was stained with silver by means of physical development according to Gallyas (1979) (link). The sections were first put into 100% ethanol, and then immersed in a 2:1 solution of pyridine and acetic acid for 30 minutes. After rinsing they were brought into an ammonium-silver-nitrate solution and after rinsing them in 0.5% acetic acid, the sections were immersed in the optimal physical developer solution for room temperature (Gallyas, 1979 (link)) until the sections showed a good stain-intensity, checked under microscope. Then the development of the staining was stopped in 0.5% acetic acid and the sections were dehydrated and mounted with Histomount.
Publication 2010
Age- and sex-matched PGRN-deficient mice and their WT littermates were anesthetized with sodium pentobarbital and transcardially perfused with 0.9% saline followed by 4% paraformaldehyde (PFA) in PBS, pH 7.4. The brains were dissected out, postfixed in 4% PFA for 24 h, and cryopreserved in 30% sucrose/PBS for 48 h. Snap-frozen brains were embedded in tissue embedding freezing medium and sectioned at a 40-µm thickness using a cryostat. Coronal sections were collected in PBS and processed free floating for immunohistochemistry.
Coronal brain sections spanning the cortex, thalamus, and hippocampus were washed in PBS, and endogenous peroxidase was quenched by incubation in 3% hydrogen peroxide/10% methanol solution for 10 min. Sections were washed in PBS and blocked in 10% normal goat serum (NGS), 0.1% Triton X-100 in PBS for 1 h at room temperature. Next, sections were incubated with various antibodies: rabbit anti-PGRN (1:1,000; Zhu et al., 2002 (link)), rat monoclonal anti-CD68 (1:500; AbD Serotec), mouse monoclonal antiubiquitin (1:50,000; Millipore), rabbit polyclonal anti-GFAP (1:2,000; Dako), mouse monoclonal anti–phospho–TDP-43 (pS409/410; 1:500; provided by H. Akiyama, M. Hasegawa, and T. Arai, Tokyo Institute of Psychiatry, Tokyo, Japan; Inukai et al., 2008 (link)), and rabbit polyclonal anti–TDP-43 (Proteintech) in 2% NGS, 0.01% Triton X-100 in PBS for 16 h at 4°C. Sections were washed in PBS and incubated with appropriate biotinylated secondary antibodies (Jackson ImmunoResearch Laboratories, Inc.) in PBS for 1 h at room temperature. After incubation in streptavidin ABC enhancer solution (Vector Laboratories) for 30 min at room temperature, immunostaining was visualized with diaminobenzidine (DAB; Sigma-Aldrich) as the chromogen. Sections were washed and mounted on precoated slides (Superfrost Plus; VWR) and allowed to air dry. The sections were further counterstained with either cresyl violet acetate or thionin (Sigma-Aldrich). The slides were dehydrated in ascending series of ethanol, passed through xylene, and coverslipped with DPX mounting media (Electron Microscopy Science). Images were acquired using a digital camera (Coolpix 5000; Nikon).
Publication 2010
Antibodies azo rubin S Brain Cloning Vectors Cortex, Cerebral cresyl violet acetate Electron Microscopy Ethanol Fingers Glial Fibrillary Acidic Protein Goat Immunohistochemistry Methanol Mice, House Normal Saline paraform Pentobarbital Sodium Peroxidase Peroxides protein TDP-43, human Rabbits Seahorses Serum Streptavidin Sucrose Thalamus Thionins Tritium Triton X-100 Xylene
Cryosections of OCT–embedded tissue blocks were transferred to PEN membrane glass slides and stained with cresyl violet acetate. Adjacent sections were H&E stained for pathology review. Laser capture microdissection was performed on a PALM MicroBeam microscope (Zeiss), collecting at least 1000 cells per compartment. RNA was extracted and libraries prepared using the Ovation RNA-Seq System V2 kit (NuGEN). Libraries were sequenced to a depth of 30 million, 100bp, single-end reads.
Publication 2019
Arecaceae Cells cresyl violet acetate Cryoultramicrotomy Laser Capture Microdissection Microscopy RNA-Seq Tissue, Membrane Tissues

Most recents protocols related to «Cresyl violet acetate»

After preparing the tissue sections as explained above, they were immersed in cresyl violet solution (0.25% cresyl violet + 0.8% glacial acetic acid + 0.6 mM sodium acetate)18 (link). Thereafter, the sections were rinsed, dehydrated, cleared, mounted for observation, and photographed by an optical microscope94 .
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Publication 2024
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Cresyl violet (CV) stains the endoplasmic reticulum and the cellular nuclei in dark purple, which includes, in the brain, cell bodies of neurons and glial cells (Eilam-Altstädter et al., 2021) (link). The protocol followed guidelines of US Army Inst Pathol (Luna et al., 1968) , in which the sections were hydrated first, submerged for 1h15 in 0.01% Cresyl violet (Sigma Aldrich catalog #C5042) in a 0.1M acetate buffer (Anachemia, AC-8218) and 0.1M acetic acid (BDH 10001CU), and then dehydrated.
Publication 2024
Cresyl violet (CV) stains the endoplasmic reticulum and the cellular nuclei in dark purple, which includes, in the brain, cell bodies of neurons and glial cells (Eilam-Altstädter et al., 2021 ). The protocol followed guidelines of US Army Inst Pathol (Luna and Armed Forces Institute of, 1968 ), in which the sections were hydrated first, submerged for 1 h15 in 0.01% Cresyl violet (Sigma Aldrich catalog #C5042) in a 0.1 M acetate buffer (Anachemia, AC-8218) and 0.1 M acetic acid (BDH 10001CU), and then dehydrated.
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Publication 2024

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Publication 2024

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Cresyl violet acetate is a synthetic organic compound commonly used as a biological stain in histology and microscopy. It is a purple crystalline powder that is soluble in water and alcohol. Cresyl violet acetate is primarily used for the staining and identification of Nissl substance in nerve cells and neurons.
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Cresyl violet is a histological stain used in microscopy to visualize cellular structures. It is a basic aniline dye that selectively binds to nucleic acids, staining the nuclei of cells. This allows for the identification and differentiation of various cell types in tissue samples.
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Permount is a mounting medium used in microscopy to permanently mount specimens on glass slides. It is a solvent-based, xylene-containing solution that dries to form a clear, resinous film, securing the specimen in place and providing optical clarity for microscopic examination.
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Cresyl violet acetate solution is a laboratory reagent used for staining and visualization purposes. It is a synthetic dye that can be used to stain certain cellular components in biological samples. The solution contains cresyl violet acetate dissolved in a suitable solvent.
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Superfrost Plus slides are high-quality, positively charged microscope slides designed for improved tissue adhesion and cell attachment. These slides feature a specialized coated surface that enhances the binding of biological samples, ensuring secure sample mounting and reliable results during histological and cytological applications.
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Cresyl violet acetate is a chemical compound commonly used in laboratory settings. It is a synthetic dye that has applications in various staining techniques, particularly in histology and microscopy. Cresyl violet acetate is known for its ability to stain specific cellular structures, which can aid in the visualization and analysis of biological samples.
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The BX51 microscope is an optical microscope designed for a variety of laboratory applications. It features a modular design and offers various illumination and observation methods to accommodate different sample types and research needs.

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