Alexa Fluor™ 594 生物胞素、钠盐(生物胞素 Alexa Fluor™ 594)
Alexa Fluor™ 594 生物胞素、钠盐(生物胞素 Alexa Fluor™ 594)
Invitrogen™

Alexa Fluor™ 594 生物胞素、钠盐(生物胞素 Alexa Fluor™ 594)

细胞不可透过性、可固定极性示踪剂 Alexa Fluor™ 594 生物胞素结合了红色荧光 Alexa Fluor™ 594 荧光基团及生物素和一种醛可固定伯胺了解更多信息
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货号数量
A12922250 μg
货号 A12922
价格(CNY)
5,860.00
Each
添加至购物车
数量:
250 μg
价格(CNY)
5,860.00
Each
添加至购物车
细胞不可透过性、可固定极性示踪剂 Alexa Fluor™ 594 生物胞素结合了红色荧光 Alexa Fluor™ 594 荧光基团及生物素和一种醛可固定伯胺。极性示踪剂通常用于研究细胞 - 细胞和细胞 - 脂质体融合以及膜通透性和胞饮过程中通过间隙连接或细胞摄取进行的转运。该水溶性示踪剂可通过全细胞膜片钳、离子电渗、胞饮囊泡的渗透裂解或类似方法进入细胞。生物素可用于使用经酶修饰的链霉素亲和素(包括分别可与 TSA 和 ELF™ 技术结合使用的辣根 (HRP) 和碱性磷酸酶 (AP))进行检测和后续扩增。
仅供科研使用。不可用于诊断程序。
规格
标签类型Alexa Fluor 染料
产品线Alexa Fluor
产品类型594 生物胞素
数量250 μg
试剂类型生物胞素
运输条件室温
Unit SizeEach
内容与储存
室温避光储存。

常见问题解答 (FAQ)

我注入了荧光示踪剂,但在组织固定并切片后无法检测到它,哪个环节出了问题?

•请确认您所用的示踪剂交联到蛋白质上,或具有用于固定的伯胺——酰肼、赖氨酸可固定葡聚糖或蛋白质偶联物皆可。
•使用醛类固定剂交联示踪剂上的胺基。
•注入更大量或更高浓度的示踪剂。示踪剂通常注射1-20%浓度(10 mg/mL或更高)。
•确认您使用正确的荧光滤光片进行检测。您可吸取少量未稀释的示踪剂储液滴一滴到载玻片上,然后在显微镜下使用您所需的滤光片观察测试。这可验证示踪剂荧光是否可以被检测到,以及荧光显微镜的滤光片是否工作正常。
•回顾组织固定和处理步骤,确认是否存在可能影响示踪剂的试剂或处理步骤。

我用Alexa Fluor偶联生物胞素标记我的神经元以观察运输,但我想只检测逆向运输而生物胞素,似乎在同时逆向和顺向运输。 我该怎么办?

观察到这两种类型的运输是生物胞素的典型特征。带有标记的霍乱毒素B类的产品只进行逆向运输。

你们有类似于荧光黄(Lucifer Yellow)但颜色不同的神经元示踪剂吗?

Lucifer Yellow CH是一个酰肼,所以我们任一Alexa Fluor或荧光标记的酰肼产品都适于此用途。此类产品的清单请见此处(https://www.thermofisher.com/us/en/home/life-science/cell-analysis/cell-tracing-tracking-and-morphology/neuronal-tracing/hydrazides-biocytins.html#prd)。

I injected a fluorescent tracer, but cannot detect it after tissue is fixed and sectioned. What am I doing wrong?

Confirm that the tracer you are using crosslinks to proteins or has a primary amine for fixation-either a hydrazide, lysine fixable dextran, or a protein conjugate.
Use aldehyde-based fixatives to cross link the amines on the tracer.
Inject a larger amount or higher concentration of the tracer. Tracers are generally injected at 1-20% concentrations (10 mg/mL or higher).
Confirm that you are using the correct fluorescent filter for detection. You can perform a spot test by pipetting a small amount of the undiluted stock solution of the tracer onto a slide, then view under the filter you are using on your microscope. This will confirm if the tracer fluorescence can be detected and the fluorescent microscope filter is working properly.
Review tissue fixation and handling procedures to confirm if any reagents or processing procedures could be affecting the tracer.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

I have labeled my neurons with an Alexa Fluor conjugated biocytin to look at transport but I wanted to examine only retrograde transport and biocytin appears to be moving retrograde and anterograde. What should I do?

Observing both types of transport is typical for biocytin. The conjugated cholera toxin subunit B products have been observed to travel only retrogradely.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

引用和文献 (11)

引用和文献
Abstract
OLIG gene targeting in human pluripotent stem cells for motor neuron and oligodendrocyte differentiation.
Authors:Liu Y, Jiang P, Deng W,
Journal:Nat Protoc
PubMed ID:21527921
Pluripotent stem cells can be genetically labeled to facilitate differentiation studies. In this paper, we describe a gene-targeting protocol to knock in a GFP cassette into key gene loci in human pluripotent stem cells (hPSCs), and then use the genetically tagged hPSCs to guide in vitro differentiation, immunocytochemical and electrophysiological ... More
Panglial gap junctional communication is essential for maintenance of myelin in the CNS.
Authors:Tress O, Maglione M, May D, Pivneva T, Richter N, Seyfarth J, Binder S, Zlomuzica A, Seifert G, Theis M, Dere E, Kettenmann H, Willecke K,
Journal:J Neurosci
PubMed ID:22649229
'In this study, we have investigated the contribution of oligodendrocytic connexin47 (Cx47) and astrocytic Cx30 to panglial gap junctional networks as well as myelin maintenance and function by deletion of both connexin coding DNAs in mice. Biocytin injections revealed complete disruption of oligodendrocyte-to-astrocyte coupling in the white matter of 10- ... More
Reaching out for signals: filopodia sense EGF and respond by directed retrograde transport of activated receptors.
Authors:Lidke DS, Lidke KA, Rieger B, Jovin TM, Arndt-Jovin DJ
Journal:J Cell Biol
PubMed ID:16103229
'ErbB1 receptors situated on cellular filopodia undergo systematic retrograde transport after binding of the epidermal growth factor (EGF) and activation of the receptor tyrosine kinase. Specific inhibitors of the erbB1 receptor tyrosine kinase as well as cytochalasin D, a disruptor of the actin cytoskeleton, abolish transport but not free diffusion ... More
Layer-specific experience-dependent rewiring of thalamocortical circuits.
Authors:Wang L, Kloc M, Gu Y, Ge S, Maffei A,
Journal:J Neurosci
PubMed ID:23447625
Thalamocortical circuits are central to sensory and cognitive processing. Recent work suggests that the thalamocortical inputs onto L4 and L6, the main input layers of neocortex, are activated differently by visual stimulation. Whether these differences depend on layer-specific organization of thalamocortical circuits; or on specific properties of synapses onto receiving ... More
Complex autonomous firing patterns of striatal low-threshold spike interneurons.
Authors:Beatty JA, Sullivan MA, Morikawa H, Wilson CJ,
Journal:J Neurophysiol
PubMed ID:22572945
During sensorimotor learning, tonically active neurons (TANs) in the striatum acquire bursts and pauses in their firing based on the salience of the stimulus. Striatal cholinergic interneurons display tonic intrinsic firing, even in the absence of synaptic input, that resembles TAN activity seen in vivo. However, whether there are other ... More