SBFI,AM,细胞通透性
SBFI,AM,细胞通透性
Invitrogen™

SBFI,AM,细胞通透性

SBFI 是一种钠敏感分子,用于测定分离线粒体中 Na+ 梯度、细胞内 NA+ 水平、细胞中 Na+ 外排,还可与其他荧光指示剂结合使用,以将细胞内了解更多信息
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货号数量
S12631 mg
货号 S1263
价格(CNY)
10,685.00
Each
添加至购物车
数量:
1 mg
价格(CNY)
10,685.00
Each
添加至购物车
SBFI 是一种钠敏感分子,用于测定分离线粒体中 Na+ 梯度、细胞内 NA+ 水平、细胞中 Na+ 外排,还可与其他荧光指示剂结合使用,以将细胞内 Na+ 的变化与 Ca2+ 和 Mg2+ 浓度、细胞内 pH 和膜电位关联起来。尽管 SBFI 对 Na+ 的选择性低于钙指示剂(如 fura-2),但在存在其他单价阳离子的情况下,其足以检测生理浓度的 Na+。SBFI 与离子结合后的光谱响应允许进行激发比测量,该指示剂可与用于 Fura-2 的相同光学滤光片和设备配合使用。

了解更多有关离子指示剂(包括钙、钾、pH 值和膜电位指示剂)的信息›

荧光离子指示剂规格:
• 标记(激发/发射波长):SBFI (∼340,380/500 nm)
• 冻干产品可以溶解在 DMSO 中,以供使用
•通常,通过向含细胞的培养基中添加溶解指示剂将产品上样至细胞中


选择性注意事项和细胞上样策略
在不存在 Na+ 的情况下,SBFI 针对 Na+ 的解离常数 (Kd) 为 3.8 mM,在 Na+ 和 K+ 合计浓度为 135 mM(接近生理离子强度)的溶液中,该值为 11.3 mM。SBFI 对 Na+ 的选择性为 K+ 的 ∼18 倍。

SBFI 有不可渗透细胞的酸盐 (S1262) 和可渗透细胞的乙酰氧基甲基 (AM) 酯(S1263S1264)两种规格。可使用我们的 Influx™ 胞饮细胞上样试剂(I14402螯合物、校准缓冲液、离子载体和细胞上样试剂—第 19.8 节)或通过显微注射、膜片移液管输注或电穿孔将阴离子酸形式上样至细胞中。对于 AM 酯上样(细胞内离子指示剂的上样和校准—注释 19.1),通常需要添加 Pluronic™ F-127 (P3000MP, P6866, P6867) 或 PowerLoad™ (P10020) 分散剂,以及相对较长的孵育时间—长达 4 小时—。

查找 Na+ 和 K+ 的荧光指示剂
我们提供了许多用于测量 Na+ 和 K+ 的荧光指示剂。有关这些产品的更多信息,请查看 Molecular Probes™ 手册中的荧光 Na+ 和 K+ 指示剂—第 21.1 节

供研究使用。不可用于人或动物的治疗或诊断。
仅供科研使用。不可用于诊断程序。
规格
检测方法荧光
染料类型钠指示剂
数量1 mg
运输条件室温
适用于(应用)细胞活力与增殖
适用于(设备)荧光显微镜
产品类型SBFI AM
Unit SizeEach
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 (281)

引用和文献
Abstract
Glutamate release evoked by glutamate receptor agonists in cultured chick retina cells: modulation by arachidonic acid.
Authors:Duarte CB,Santos PF,Sánchez-Prieto J,Carvalho AP
Journal:Journal of neuroscience research
PubMed ID:8739156
Cultured chick-embryo heart cells respond differently to ouabain as measured by the increase in their intracellular Na+ concentration.
Authors:Ahlemeyer B, Weintraut H, Schoner W
Journal:Biochim Biophys Acta
PubMed ID:1420320
Using digital imaging microscopy with the sodium-sensitive fluorescent indicator sodium-binding benzofuran isophtalate (SBFI), we examined the cytosolic free sodium ion concentration ([Na+]i) in single chick-embryo heart cells. The distribution of the [Na+]i was homogeneous within one cell, but we found a wide cell to cell variation in the range of ... More
Effect of vasopressin on Na+ kinetics in cultured rat vascular smooth muscle cells.
Authors:Okada K, Ishikawa S, Saito T
Journal:Biochem Biophys Res Commun
PubMed ID:2124111
The effect of arginine vasopressin (AVP) on Na+ kinetics was examined in cultured rat vascular smooth muscle cells (VSMC) and rat renal papillary collecting tubule cells (RPCT) by the direct measurement of intracellular sodium concentration [(Na+]i) using fluorescence dye; SBFI. AVP increased [Na+]i in a dose-dependent manner at a concentration ... More
Mechanism of collagen activation in human platelets.
Authors:Roberts DE, McNicol A, Bose R
Journal:J Biol Chem
PubMed ID:14981087
The mechanism of collagen-induced human platelet activation was examined using Ca2+, Na+, and the pH-sensitive fluorescent dyes calcium green/fura red, sodium-binding benzofuran isophthalate, and 2',7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein. Administration of a moderate dose of collagen (10 microg/ml) to human platelets resulted in an increase in [Ca2+](i) and platelet aggregation. The majority of this ... More
Expression of the voltage-gated sodium channel NaV1.5 in the macrophage late endosome regulates endosomal acidification.
Authors:Carrithers MD, Dib-Hajj S, Carrithers LM, Tokmoulina G, Pypaert M, Jonas EA, Waxman SG,
Journal:J Immunol
PubMed ID:17548620
'Voltage-gated sodium channels expressed on the plasma membrane activate rapidly in response to changes in membrane potential in cells with excitable membranes such as muscle and neurons. Macrophages also require rapid signaling mechanisms as the first line of defense against invasion by microorganisms. In this study, our goal was to ... More