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Citations & References (702)
Invitrogen™
Lucifer Yellow CH, Lithium Salt, 25 mg
ルシファーイエローCH、リチウム塩は、428/536 nmの励起／発光ピークを持つ水溶性染料です。このツールは、カルボヒドラジド（CH）基が含まれているため、アルデヒド固定時に周囲の生体分子と共有結合することができ、神経細胞の形態を研究するためのお気に入りのツールです詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| L453 | 25 mg |
製品番号（カタログ番号） L453
価格（JPY）お問い合わせください ›
34,600
Each
数量:
25 mg
ルシファーイエローCH、リチウム塩は、428/536 nmの励起／発光ピークを持つ水溶性染料です。このツールは、カルボヒドラジド（CH）基が含まれているため、アルデヒド固定時に周囲の生体分子と共有結合することができ、神経細胞の形態を研究するためのお気に入りのツールです。ルシファーイエローCHのリチウム塩の形態は、ルシファーイエローCHのカリウムおよびアンモニウム塩の形態よりも高い溶解度を有するため、マイクロインジェクションに一般的に使用されます。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
色黄色
検出法蛍光
使用対象 (装置)蛍光顕微鏡
分子量457.24
製品タイプリチウム塩
数量25 mg
出荷条件室温
細胞内局在細胞質&サイトゾル
Excitation/Emission428/536 nm
Unit SizeEach
組成および保存条件
室温で保存し、光から保護します。
引用および参考文献 (702)
引用および参考文献
Abstract
Endothelial and smooth muscle cell conduction in arterioles controlling blood flow.
Journal:Am J Physiol
PubMed ID:9458866
We performed intracellular recording with Lucifer yellow dye microinjection to investigate the cellular pathway(s) by which constriction and dilation are conducted along the wall of arterioles (diameter 47 +/- 1 microns, n = 63) supplying blood flow to the cheek pouch of anesthetized hamsters. At rest, membrane potential (Em) of
Bursting response to current-evoked depolarization in rat CA1 pyramidal neurons is correlated with lucifer yellow dye coupling but not with the presence of calbindin-D28k.
Journal:Synapse
PubMed ID:2042109
Calbindin-D28k (CaBP) immunohistochemistry has been combined with electrophysiological recording and Lucifer Yellow (LY) cell identification in the CA1 region of the rat hippocampal formation. CaBP is shown to be contained within a distinct sub-population of CA1 pyramidal cells which is equivalent to the superficial layer described by Lorente de Nó
Membrane conductance oscillations in astrocytes induced by phorbol ester.
Journal:Nature
PubMed ID:3627267
Glial cells in the central nervous systems (CNS) have complex functions which are difficult to decipher because of the intimate intertwining of glial cells with neurons. We have therefore developed an essentially neuron-free preparation of CNS astrocytes in the kainic acid lesioned hippocampal slice. With this preparation we have examined
Deformation of network connectivity in the inferior olive of connexin 36-deficient mice is compensated by morphological and electrophysiological changes at the single neuron level.
Journal:J Neurosci
PubMed ID:12805309
Compensatory mechanisms after genetic manipulations have been documented extensively for the nervous system. In many cases, these mechanisms involve genetic regulation at the transcription or expression level of existing isoforms. We report a novel mechanism by which single neurons compensate for changes in network connectivity by retuning their intrinsic electrical
Dual fluorescence combined with a two-color immunoperoxidase technique: a new way of visualizing diverse neuronal elements.
Journal:J Neurosci Methods
PubMed ID:1712061
'A method is described that allows an estimation of the neurotransmitter-related immunoreactivity, morphology and relationship to other immunoreactive elements, of single functionally identified neurons in the central nervous system. First, neurons are identified electrophysiologically using intracellular recording and labelled by iontophoresis of lucifer yellow (LY). After fixation and sectioning of