X-Rhod-1,AM,细胞通透性 - 特殊包装
Invitrogen™

X-Rhod-1,AM,细胞通透性 - 特殊包装

标记的钙指示剂,结合 Ca2+ 后荧光增强
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货号数量
X1421010 x 50 μg
货号 X14210
价格(CNY)
4,583.00
飞享价
Ends: 31-Dec-2026
6,278.00
共减 1,695.00 (27%)
10 x 50 µg
数量:
10 x 50 μg
价格(CNY)
4,583.00
飞享价
Ends: 31-Dec-2026
6,278.00
共减 1,695.00 (27%)
10 x 50 µg

Labeled calcium indicators are molecules that exhibit an increase in fluorescence upon binding Ca2+. They have uses in many calcium signaling investigations, including measuring Ca2+ in cells and tissues that have high levels of autofluorescence and also for detecting Ca2+ release generated by photoreceptors and photoactivatable chelators. Cells may be loaded with the AM ester forms of these calcium indicators by adding the dissolved indicator directly to dishes containing cultured cells. The fluorescence signal from these cells is generally measured using fluorescence microscopy.

  • 用于多种钙信号传导研究,包括细胞和组织中 Ca2+ 的测定
  • 可通过直接向含培养细胞的培养皿中添加溶解的指示剂,将这些钙指示剂的 AM 酯形式上样至细胞中
  • 通常使用荧光显微镜检测这些细胞的荧光信号
  • 在结合 Ca2+ 之后荧光增加,波长稍有迁移
  • 另外,基于 BAPTA 的指示剂可结合各种重金属阳离子(例如 Mn2+、Zn2+、Pb2+),亲和力远高于 Ca2+
  • 由于存在这些离子而引起的钙测量的扰动可以使用重金属选择性螯合剂进行控制
  • 标签(Ca2+–结合形式的 Ex/Em):X-rhod-1 (580/602nm)
  • 结合 Ca2+ 后荧光强度增加:>100 倍
  • 在不含 Mg2+的缓冲液中,Ca2+ 的 Kd:约700nM

钙检测、细胞分析、细胞活率、增殖和功能、离子稳态及信号传导

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X-rhod-1
数量10 x 50 μg
运输条件室温
发射波长范围602 nm
Excitation Wavelength Range580 nm
适用于(应用)Calcium Indicator
适用于(设备)荧光显微镜
产品类型染料
Unit Size10 x 50 µg
内容与储存
在冷冻冰箱(-5°C 至 -30°C)中避光储存。

引用和文献 (40)

引用和文献
Abstract
Mitochondrial modulation of Ca2+ -induced Ca2+ -release in rat sensory neurons.
Authors:Jackson JG, Thayer SA
Journal:J Neurophysiol
PubMed ID:16760347
'Ca2+ -induced Ca2+ -release (CICR) from ryanodine-sensitive Ca2+ stores provides a mechanism to amplify and propagate a transient increase in intracellular calcium concentration ([Ca2+]i). A subset of rat dorsal root ganglion neurons in culture exhibited regenerative CICR when sensitized by caffeine. [Ca2+]i oscillated in the maintained presence of 5 mM ... More
Selective, high-resolution fluorescence imaging of mitochondrial Ca2+ concentration.
Authors:Gerencsér AA AA, Adam-Vizi V
Journal:Cell Calcium
PubMed ID:11733937
'We have developed a digital image processing technique based on highpass filtering of microfluorimetric images for selective transmission of fine image details corresponding to mitochondria. This technique enabled the detection of the mitochondrial calcium signals with high selectivity, simultaneously with the cytosolic calcium signal. The validity of this technique was ... More
Use of fluorescent Ca2+ dyes with green fluorescent protein and its variants: problems and solutions.
Authors:Bolsover S, Ibrahim O, O'luanaigh N, Williams H, Cockcroft S
Journal:Biochem J
PubMed ID:11368760
'We have studied the degree to which fluorescent Ca(2+) indicator dyes, and green fluorescent protein and its variants, can be used together. We find that the most commonly used fluorescent protein, enhanced green fluorescent protein (EGFP), seriously contaminates fura 2 signals. We suggest two alternative combinations for which there is ... More
CXCR4 regulates growth of both primary and metastatic breast cancer.
Authors:Smith MC, Luker KE, Garbow JR, Prior JL, Jackson E, Piwnica-Worms D, Luker GD
Journal:Cancer Res
PubMed ID:15574767
'The chemokine receptor CXCR4 and its cognate ligand CXCL12 recently have been proposed to regulate the directional trafficking and invasion of breast cancer cells to sites of metastases. However, effects of CXCR4 on the growth of primary breast cancer tumors and established metastases and survival have not been determined. We ... More
A novel method for assessing effects of hydrostatic fluid pressure on intracellular calcium: a study with bovine articular chondrocytes.
Authors:Mizuno S
Journal:Am J Physiol Cell Physiol
PubMed ID:15643052
'Chondrocytes in articular cartilage are exposed to hydrostatic pressure and distortional stress during weight bearing and joint loading. Because these stresses occur simultaneously in articular cartilage, the mechanism of mechanosignal transduction due to hydrostatic pressure alone in chondrocytes is not clear. In this study, we attempted to characterize the change ... More