Cresyl Violet acetate structure
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Common Name | Cresyl Violet acetate | ||
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CAS Number | 10510-54-0 | Molecular Weight | 321.330 | |
Density | N/A | Boiling Point | 468.3ºC | |
Molecular Formula | C18H15N3O3 | Melting Point | 140-143 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 237ºC |
Use of Cresyl Violet acetateCresyl violet acetate is a red fluorescent stain, which can be used to stain neurons. |
Name | cresyl violet acetate |
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Synonym | More Synonyms |
Description | Cresyl violet acetate is a red fluorescent stain, which can be used to stain neurons. |
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Related Catalog | |
In Vitro | The estimated total number of SG neurons is 27,485±3251 and 26,705±1823 in the PV and Cresyl violet acetate stained sections, respectively. There is no significant difference between them (p=0.552). Therefore, Cresyl violet acetate staining is simpler and more cost effective when estimates neuronal number. Although PV stains spiral ganglion neurons (SGNs) with a greater intensity and provides a functional status, its tedious protocol limits its use for quantification. Total RC volume is estimated using probe and it is found that an average RC volume of 2.162±0.35 mm3 and 1.82±0.33 mm3 in Cresyl violet acetate staining and PV immunostaining sections, respectively. Volume of neurons is estimated using nucleator probe and it is 3487.63±951 μm3 and 3740.1±784 μm3 in Cresyl violet acetate staining and PV immunostaining sections, respectively. Similarly, volume of neuronal nucleus is also estimated using nucleator probe and it is found to be 131.68±50 μm3 and 126.51±33 μm3 in Cresyl violet acetate staining and PV immunostaining sections, respectively[1]. |
Cell Assay | Cochlear sections containing SGNs are placed in 24 wells plates containing PBS (pH 7.4) and stored at 4°C. The sections are then used for Cresyl violet acetate and immunohistochemical (IHC) staining. Every 7th section is stained with Cresyl violet acetate (1%), dehydrated with ascending grades of alcohol, cleared with xylene, mounted with DPX and observed under microscope. Approximately 12-13 Cresyl violet acetate staining sections from each specimen are used for stereology. None of these cases show any histopathological changes under the light microscope. Estimation of the total volume of the Rosenthal canal (RC), total number of SGNs (optical fractionator probe) and the volume of the soma and their nucleus (nucleator probe) is done with software[1]. |
References |
Boiling Point | 468.3ºC |
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Melting Point | 140-143 °C(lit.) |
Molecular Formula | C18H15N3O3 |
Molecular Weight | 321.330 |
Flash Point | 237ºC |
Exact Mass | 321.111328 |
PSA | 113.20000 |
LogP | 3.91930 |
Vapour Pressure | 6.07E-09mmHg at 25°C |
Stability | Stable. Incompatible with strong oxidizing agents. |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi: Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S37/39-S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
Orthotopic transplantation of immortalized mesencephalic progenitors (CSM14.1 cells) into the substantia nigra of hemiparkinsonian rats induces neuronal differentiation and motoric improvement.
J. Anat. 212(1) , 19-30, (2008) Neural progenitor cell grafting is a promising therapeutic option in the treatment of Parkinson's disease. In previous experiments we grafted temperature-sensitive immortalized CSM14.1 cells, derived ... |
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Analysis and testing of biological stains--the Biological Stain Commission Procedures.
Biotech. Histochem. 77(5&6) , 237-275, (2002)
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The terminal pathway of the complement system is activated in focal penetrating but not in mild diffuse traumatic brain injury.
J. Neurotrauma 30(23) , 1954-65, (2013) The complement system plays an important role in the inflammatory response activated by many central nervous system disorders. However, its significance in traumatic diffuse traumatic axonal injury (T... |
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