细胞渗透性 indo-1, AM——特殊包装
细胞渗透性 indo-1, AM——特殊包装
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细胞渗透性 indo-1, AM——特殊包装

该可渗透细胞的 indo-1, AM 是紫外光可激发的比率式 Ca2+ 指示剂。当染料与 Ca2+ 饱和结合时,不含 Ca2+了解更多信息
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货号数量
I122320 x 50 μg
货号 I1223
价格(CNY)
4,807.00
Each
添加至购物车
数量:
20 x 50 μg
价格(CNY)
4,807.00
Each
添加至购物车
该可渗透细胞的 indo-1, AM 是紫外光可激发的比率式 Ca2+ 指示剂。当染料与 Ca2+ 饱和结合时,不含 Ca2+ 的培养基中 indo-1 的发射上限值可从 ∼475 nm 偏移至 ∼400 nm。可在 1 mg (I-1203) 和 1 mM 溶液 (I-1226) 中获得呈这种 AM 酯形式的染料。还可提供呈不可渗透细胞的五钾 (F-1202) 盐形式的染料。

了解有关离子指示剂(包括钙、钾、pH 值和膜电位指示剂)的更多信息›

仅供科研使用。不可用于诊断程序。
规格
检测方法荧光
染料类型基于荧光染料
形式实心
数量20 x 50 μg
运输条件室温
适用于(应用)细胞活力、增殖与细胞成像, 流式细胞分析
适用于(设备)荧光显微镜, 显微光度计, 流式细胞仪
产品类型Indo-1 AM
Unit SizeEach
内容与储存
在冷冻冰箱(-5°C 至 -30°C)中避光储存。

常见问题解答 (FAQ)

使用流式细胞仪时,可以使用什么指示染料来测定钙离子流?

Indo-1,AM流式细胞仪的首选染料。它更适用于单激光激发(通常使用351-364 nm的氩离子激光的谱线),可监视两个发射。Indo-1的最大发射从在无Ca2+培养基中的〜475 nm变为Ca2+饱和的〜400 nm。Indo-1,AM是特别适用于多色荧光应用。

I am doing calcium flux imaging with your Fura-2 calibration kit, but am seeing a large variability in ratio in different places around the slide. I am correcting for uniform illumination, using the product as directed, and sealing the coverslip with nail polish.

The nail polish may be the problem. The Kd value (calcium sensitivity) changes depending upon the dye's environment. Nail polish has solvents that can leech under the coverslip and cause variability. We recommend either going without a sealing or sealing with melted paraffin painted on the coverslip edges with a cotton-tipped applicator (paraffin is hydrophobic and has no solvents).

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

I need to label cells with Fluo-4, AM, for a calcium flux assay. How long after labeling will the dye be retained?

After loading dye into the cells, intracellular esterases remove the 'AM' moiety from the dye. When the 'AM' group is removed, the dye is able to bind calcium and fluoresce. Since the dye is not covalently bound to any cellular components, it may be actively effluxed from the cell. The rate of efflux is dependent upon the inherent properties of the cell, culture conditions and other factors. The dye may be retained for hours, days or even weeks or lost in a matter of minutes. The use of Probenecid (Cat. No. P36400) limits loss by active efflux.

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

What indicator dye can I use to measure calcium flux by flow cytometry?

Indo-1, AM is the preferred stain for flow cytometry, where it is more practical to use a single laser for excitation, usually the 351–364 nm spectral lines of the argon-ion laser, and monitor two emissions. The emission maximum of Indo-1 shifts from ~475 nm in Ca2+-free medium to ~400 nm when the dye is saturated with Ca2+. Indo-1, AM is particularly suited for multicolor fluorescence applications.

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

引用和文献 (1099)

引用和文献
Abstract
Modulation of myocardial function and [Ca2+] sensitivity by moderate hypothermia in guinea pig isolated hearts.
Authors:Stowe DF,Fujita S,An J,Paulsen RA,Varadarajan SG,Smart SC
Journal:The American journal of physiology
PubMed ID:10600852
FDF03, a novel inhibitory receptor of the immunoglobulin superfamily, is expressed by human dendritic and myeloid cells.
Authors:Fournier N,Chalus L,Durand I,Garcia E,Pin JJ,Churakova T,Patel S,Zlot C,Gorman D,Zurawski S,Abrams J,Bates EE,Garrone P
Journal:Journal of immunology (Baltimore, Md. : 1950)
PubMed ID:10903717
CD5 antibodies increase intracellular ionized calcium concentration in T cells.
Authors:June CH,Rabinovitch PS,Ledbetter JA
Journal:Journal of immunology (Baltimore, Md. : 1950)
PubMed ID:3106489
The binding of a variety of monoclonal antibodies to the CD5 (T, gp67) pan T cell differentiation antigen has been shown to potentiate T cell proliferation. In this paper we show that CD5 monoclonal antibodies cause increased intracellular free calcium concentration ([Ca2+]i) in T cells. An increase in [Ca2+]i occurred ... More
The role of L-type Ca2+ current and Na+ current-stimulated Na/Ca exchange in triggering SR calcium release in guinea-pig cardiac ventricular myocytes.
Authors:Evans AM, Cannell MB
Journal:Cardiovasc Res
PubMed ID:9349392
OBJECTIVE: This study examines the relative ability of sodium current (INa)-stimulated reverse mode Na/Ca exchange and the L-type calcium current (ICa) to trigger calcium-induced calcium release (CICR) in guinea-pig ventricular myocytes. METHODS: Cytosolic Ca2+ transients were recorded from enzymatically dissociated guinea-pig ventricular myocytes using Indo-1. Macroscopic membrane currents were simultaneously ... More
Nitric oxide is an upstream signal of vascular endothelial growth factor-induced extracellular signal-regulated kinase1/2 activation in postcapillary endothelium.
Authors:Parenti A, Morbidelli L, Cui XL, Douglas JG, Hood JD, Granger HJ, Ledda F, Ziche M
Journal:J Biol Chem
PubMed ID:9461619
We recently demonstrated that nitric oxide (NO) significantly contributes to the mitogenic effect of vascular endothelial growth factor (VEGF), suggesting a role for the NO pathway in the signaling cascade following kinase-derivative receptor activation in vascular endothelium. The aim of this study was to investigate the intracellular pathways linked to ... More