"Staining Solutions"
Schaeffer and Fulton Spore Stain Solution A, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
In Schaeffer-Fulton`s method, a primary stain-malachite green is forced into the spore by steaming the bacterial emulsion. Malachite green is water soluble and has a low affinity for cellular material, so vegetative cells may be decolorized with water. Ve
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Soluzione di Shorr stain for histology, Sigma-Aldrich®
Supplier: Merck
For the diagnosis of hormonal disorders in cytology
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PageBlue™ protein staining solution
Supplier: Thermo Fisher Scientific
PageBlue Protein Staining Solution is a sensitive, economical formulation of colloidal coomassie G-250 dye for endpoint staining of proteins in polyacrylamide gels and on PVDF membranes without methanol or acetic acid.
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Cresyl Violet Stain Solution (1%), Abcam
Supplier: Abcam
Cresyl Violet Stain Solution (1%) ab246817 is designed for staining Nissl substance in neurons on formalin fixed, paraffin-embedded tissue.
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Cresyl Violet Stain Solution (0.1%), Abcam
Supplier: Abcam
Cresyl violet stain solution (0.1%) is a staining solution for visualizing Nissl substance in neurons on formalin-fixed, paraffin-embedded tissue. - Stains Nissl granules violet and neuroglia nuclei slightly bluer - Ideal for cerebral cortex tissue analysis
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Lactophenol blue solution stain (fungal), Sigma-Aldrich®
Supplier: Merck
Lactophenol blue solution for staining fungi.
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Methylene Blue Stain Solution, Abcam
Supplier: Abcam
Methylene Blue Stain Solution ab246830 has been optimized to give outstanding results when used in various procedures such as the Ziehl-Neelsen, Fite's, and Gram stain.
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Gram's decolourising solution for Gram staining, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Gram staining is one of the most significant staining techniques in microbiology. Gram′s decolouriser solution is a mixture of ethanol and acetone. Gram′s decolouriser solution is used in Gram staining procedure, after the iodine step to remove the crystal violet dye. The decolouriser dissolves the lipid layer from the gram-negative cells.
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Papanicolaou's solution 2a Orange G (OG 6) used in nuclear staining, for cytology, J.T.Baker®
Supplier: Avantor
Papanicolaou (PAP) staining solution is specifically designed for diagnosis applications.
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Gram′s safranin solution for Gram staining, per microscopia, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Gram’s safranin solution, also known as Safranin T or Basic Red 2, is a ready-to-use staining solution that comprises 10% safranin in ethanol. Safranin is a basic, cationic, azine dye containing a planar, diaminophenazine chromophore, with a phenyl substituent attached to a ring nitrogen. The trimethyl cationic form of safranine is lipophilic, whereas the dimethyl forms are weakly hydrophilic. It is most notably used in bacteriology as a counterstain in Gram staining to differentiate between Gram-positive and Gram-negative bacteria.
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Ponceau S 0,1 % (w/v) in 5% acetic acid staining solution
Supplier: Biotium
Ponceau S staining solution is used for the detection of proteins on PVDF and nitrocellulose membranes with a limit of detection of about 250 ng of transferred protein.
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Papanicolaou's solution 2b Orange II solution stain for cytology, Sigma-Aldrich®
Supplier: Merck
Cytoplasm staining of mature and keratinized cells in cytology
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Gram's decolourising solution for Gram staining, Sigma-Aldrich®
Supplier: Merck
Used for Gram staining
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Papanicolaou's solution 1b Hematoxylin solution S used in nuclear staining, for cytology, Sigma-Aldrich®
Supplier: Merck
Nuclear staining in cytology
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No Cal stain lifter solution, Orion™
Supplier: Thermo Orion
This cleaning solution restores proper electrode performance and prolongs the useful life of the electrode.
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Coomassie® Blu brillante R-250 protein stain, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Brilliant Blue R staining solution is especially designed for use in staining protein in agarose gels following immunoelectrophoresis and Ouchterlony gels. The stain contains ethanol and acetic acid so gels do not require fixing prior to staining. The immunoelectrophoresis or Ouchterlony gel is first washed with water and saline to remove non-precipitated proteins and then dried. The gel is then immersed in staining solution for 30 min and destained with 10% acetic acid. For detection of protein bands following electrophoresis.



