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高爾基體染色試劑盒說明書PK401A PK401

最近更新時(shí)間：2012-10-26

提 供 商：上海起發(fā)實(shí)驗(yàn)試劑有限公司資料大?。?/span>529.2KB

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FD Rapid GolgiStain™ Kit （small）

fdneurotech是世界的染色試劑盒供應(yīng)商，其提供的高爾基體染色試劑盒以其高品質(zhì)的結(jié)果聞名于科研界，光2012年列出來的引用文獻(xiàn)就多達(dá)70篇，2011年更是100多篇，fdneurotech從2012年開始就和上海起福生物科技公司簽訂長(zhǎng)期合作協(xié)議為中國(guó)科研人員帶來的產(chǎn)品，并在中國(guó)設(shè)有庫(kù)存，歡迎廣大科研工作者和我們公司

Golgi-Cox impregnation^{1, 2} has been one of the most effective techniques for studying both the normal and abnormal morphology of neurons as well as glia. Using the Golgi technique, subtle morphological alterations in neuronal dendrites and dendritic spines have been discovered in the brains of animals treated with drugs as well as in the postmortem brains of patients with neurological diseases^{3, 4}. However, the unreliability and the time-consuming process of Golgi staining have been major obstacles to the widespread application of this technique

FD Rapid GolgiStain™ Kit is designed based on the principle of the methods described by Ramón- Moliner², Glaser and Van der Loos⁵. This kit has not only dramatically improved and simplified the Golgi-Cox technique but has also proven to be extremely reliable and sensitive for demonstrating morphological details of neurons and glia, especially dendritic spines. The FD Rapid GolgiStain™ Kit has been tested extensively and widely used on the brains from several species of animals as well as on the specimens of postmortem human brains.

Kit contents:

Store at room temperature

Solution A 125 ml
Solution B 125 ml
Solution C 125 ml x 2
Solution D 125 ml
Solution E 125 ml
Glass Specimen Retriever 2
Natural hair paintbrush 3
Dropping bottle 1
User Manual 1

Materials required but not included:

• Double distilled or deionized water.
• Plastic or glass tubes or vials.
• Histological supplies and equipment, including gelatin-coated microscope slides, coverslips, staining jars, ethanol, xylene or xylene substitutes, resinous mounting medium （e.g. Permount®）, and a light microscope.

References:

1. Corsi P. （1987） Camillo Golgi’s morphological approach to neuroanatomy. In Masland RL, Portera-Sanchez A and Toffano G （eds.）, Neuroplasticity: a new therapeutic tool in the CNS pathology, pp 1-7. Berlin: Springer.
2. Ramón-Moliner E. （1970） The Golgi-Cox technique. In Nauta WJH and Ebbesson SOE （eds.）, Contemporary Methods in Neuroanatomy. pp 32-55, New York: Springer.
3. Graveland GA, Williams RS, and DiFiglia M. （1985） Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington’s disease. Science. 227:770-3.
4. Robinson TE, and Kolb B. （1997） Persistent structural modification in nucleus accumbens and prefrontal cortex neurons produced by previous experience with amphetamine. J. Neurosci. 17:8491-7.
5. Glaser ME, and Van der Loos H. （1981） Analysis of thick brain sections by obverse-reverse computer microscopy: application of a new, high clarity Golgi-Nissl stain. J. Neurosci. Meth. 4:117-25.

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