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Invitrogen™ NeuroTrace™ 640/660 Deep-Red Fluorescent Nissl Stain - Solution in DMSO
Description
- Nissl staining is standard histological method for visualizing neurons in brain and spinal cord
- Composed of ribosomal RNA associated with rough endoplasmic reticulum in neuronal perikarya and dendrites, Nissl substance redistributes within cell body in injured or regenerating neurons, providing marker for physiological state of neuron
Cell Analysis, Cell Structure, Cell Tracing and Tracking, Neuronal Tracing, Nissl Bodies
Order Info
Shipping Condition: Room temperature
Specifications
Specifications
| Color | Deep Red |
| Detection Method | Fluorescence |
| Product Type | Nissl Stain |
| Quantity | 1 mL |
| Content And Storage | Store in freezer (-5 to -30°C) and protect from light. |
| Shipping Condition | Room Temperature |
| For Use With (Equipment) | Fluorescence Microscope |
| Sub Cellular Localization | Nissl Bodies |
| Excitation/Emission | 640/660 nm |
| Product Line | NEUROTRACE |
Frequently Asked Questions (FAQs)
Yes. We have done this successfully with an anti-GFAP primary and an Alexa Fluor secondary antibody. We would recommend labeling with the primary and secondary antibodies first, then following up with the standard NeuroTrace Nissl Stain protocol.
Our NeuroTrace Nissl stains label the Nissl substance which is composed of ribosomal RNA associated with the rough endoplasmic reticulum and is present in high amounts in neuronal cells. These dyes are not completely specific for neurons, but will selectively stain neurons based on their high level of protein synthesis. In some cases they may show staining of other cell types such as glia, so you may need to decrease the staining concentration to obtain more selective neuronal labeling. We suggest dilutions in the range of 20- to 300-fold for neuronal staining.
We have only tested them on mouse brain cryosections, however, there is at least one citation describing their use on paraffin tissue sections (Michelle L. Schlief, Ann Marie Craig, and Jonathan D. Gitlin. NMDA Receptor Activation Mediates Copper Homeostasis in Hippocampal Neurons. The Journal of Neuroscience, January 5, 2005, 25(1):239 - 246).
The dyes are proprietary, however they are stains that label the Nissl substance, which is composed of ribosomal RNA associated with the rough endoplasmic reticulum and is present in high amounts in neuronal cells.
Please check out this web page (https://www.thermofisher.com/us/en/home/life-science/cell-analysis/cell-tracing-tracking-and-morphology/neuronal-tracing.html) for details.
For Research Use Only. Not for use in diagnostic procedures.