Oregon Green™ 488 BAPTA-1, AM, cell permeant - Special Packaging
Oregon Green™ 488 BAPTA-1, AM, cell permeant - Special Packaging
Invitrogen™

Oregon Green™ 488 BAPTA-1, AM, cell permeant - Special Packaging

標識カルシウム指示薬は、Ca2+と結合すると蛍光が増加する分子です。Ca2+の流入と放出に続いて細胞内Ca2+を測定したり、生体組織におけるCa2+多光子励起イメージングを含む多くのカルシウムシグナル伝達研究に使用されています。培養細胞を含むディッシュに溶解インジケーターを直接添加することで、これらカルシウムインジケーターのAMエステル型を細胞に添加できます。これらの細胞からの蛍光シグナルは、一般的に蛍光顕微鏡、蛍光マイクロプレートアッセイ、またはフローサイトメトリーを使用して測定されます詳細を見る
製品番号(カタログ番号)数量
O680710 x 50 μg
製品番号(カタログ番号) O6807
価格(JPY)
90,200
Each
お問い合わせください ›
数量:
10 x 50 μg
標識カルシウム指示薬は、Ca2+と結合すると蛍光が増加する分子です。Ca2+の流入と放出に続いて細胞内Ca2+を測定したり、生体組織におけるCa2+多光子励起イメージングを含む多くのカルシウムシグナル伝達研究に使用されています。培養細胞を含むディッシュに溶解インジケーターを直接添加することで、これらカルシウムインジケーターのAMエステル型を細胞に添加できます。これらの細胞からの蛍光シグナルは、一般的に蛍光顕微鏡、蛍光マイクロプレートアッセイ、またはフローサイトメトリーを使用して測定されます。

カルシウム、カリウム、pH、膜電位インジケータなどのイオンインジケータの詳細については、こちらを参照してください›

カルシウムインジケータ(AMエステル)仕様:
•ラベル(Ex/EM):オレゴングリーン™ 488 BAPTA-1(494/523 nm)
•Ca2+結合時の蛍光強度の増加:約14倍
• Ca2+結合時の蛍光増加


Molecular Probes™カルシウムインジケーターの波長スペクトル特性のわずかな変化により
、これらのプローブは可視光によって励起され、励起に必要なエネルギーが低いため、細胞光損傷の可能性が低減されます。一般的に使用されているレーザーベースの装置(共焦点レーザースキャン顕微鏡など)は、これらのインジケータを効率的に励起でき、その放出は、細胞の自動蛍光および散乱バックグラウンドが問題にならないスペクトル領域にあります。

蛍光カルシウム指示薬の選択肢を拡大
™ 当社は、さまざまな実験シナリオで使用するMolecular Probesカルシウム指示薬を幅広く取り揃えています。たとえば、漏出の低減や区画化のためのデキストラン型や、高振幅カルシウムTransitiveを検出するためのBAPTAコンジュゲートなどです。詳細については、Molecular Probesハンドブックの「可視光で励起された蛍光Ca2+インジケータ」—セクション19.3™を参照してください。

UV-exitable Ca2+指示薬、タンパク質ベースCa2+指示薬、Ca2+指示薬のコンジュゲート用、その他の金属イオン(Mg2+、Zn2+)の蛍光ベースのインジケータ については、Molecular Probesハンドブック™のCa 2+、Mg 2+、Zn 2+およびその他の金属イオンのインジケータ—第19章を参照してください。

研究用途にのみご使用ください。動物またはヒトの治療または診断用途には使用できません。
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
検出法蛍光
染色剤タイプ蛍光色素ベース
数量10 x 50 μg
出荷条件室温
使用対象(アプリケーション)細胞の生存率と増殖
使用対象 (装置)蛍光顕微鏡, フローサイトメーター, マイクロプレートリーダー
製品ラインOregon Green
製品タイプ染色
Unit SizeEach
組成および保存条件
フリーザー(-5℃~-30℃)に保存。

よくあるご質問(FAQ)

What cellular processes can be analyzed with a flow cytometer?

-Calcium flux: Each of the Oregon Green calcium indicators binds intracellular calcium with increasing affinity, providing a sensitivity range to match many applications. Oregon Green probes emit green fluorescence at resting levels of Ca2+ and increase their fluorescence intensity 14-fold with increasing Ca2+ concentration. The cell-permeant formulation (Cat. No. O6807) can be loaded in cell media and is compatible with flow cytometry.
-Rhodamine-based calcium indicators comprise a range of probes for large or small changes in Ca2+ concentration. They exhibit a 50-fold increase in fluorescence upon calcium binding and offer a range of wavelengths that can be used in conjunction with GFP or green-fluorescent dyes for multiplexing. Rhod-2, AM (Cat. No. R1245MP), in particular, localizes to mitochondria and can be used with flow cytometry.
-Membrane potential: A distinctive feature of the early stages of apoptosis is the disruption of the mitochondria, including changes in membrane and redox potential. We offer a range of products specifically designed to assay mitochondrial membrane potential in live cells by flow cytometry, with minimal disruption of cellular function. The MitoProbe family of mitochondrial stains (Cat. Nos. M34150, M34151, and M34152) provide quick, easy, and reliable flow cytometric detection of the loss of mitochondrial membrane potential that occurs during apoptosis. MitoTracker dyes (Cat. Nos. M7510 and M7512) are membrane potential-dependent probes for staining mitochondria in live cells. The staining pattern of MitoTracker dyes is retained throughout subsequent flow cytometry immunocytochemistry, DNA end labeling, in situ hybridization, or counterstaining steps. The Mitochondrial Permeability Transition Pore Assay (Cat. No. M34153) provides a more direct method of measuring mitochondrial permeability transition pore opening than assays relying on mitochondrial membrane potential alone. The mitochondrial permeability transition pore (MPTP) is a non-specific channel formed by components from the inner and outer mitochondrial membranes, and appears to be involved in the release of mitochondrial components during cell death.
-Phagocytosis: In phagocytosis, cells internalize particulate matter such as microorganisms, and this process is important for immune responses and during the clearance of apoptotic cells. Probes for studying phagocytosis include BioParticles indicators—bacteria and yeast labeled with fluorescent dyes.
-Tracking phagocytosis using a quench/wash-based assay can report on simple uptake, or a pH indicator can be used to monitor stages in the pathway. We have no-wash assays labeled with pHrodo Red or Green (Cat. Nos. A10010, P35361, P35364, P35365, P35366, and P35367) and no-wash assays for whole blood (Cat. Nos. A10025, A10026, P35381, and P35382), all suitable for flow cytometry.
-pH changes: Sensitive pH determinations can be made in a physiological range using either fluorescent intensity or ratiometric measurements. pHrodo dyes (Cat. Nos. P35373 and P35372) provide signal intensity modulation from pH 2 to pH 9 and with a choice of fluorescent wavelengths. Tracking internalization of fluorescent dextran is a routine method for analyzing pH changes in cellular compartments. Dextran conjugates of pHrodo dyes (Cat. Nos. P35368 and P10361) provide the most complete solution by allowing discrimination of vesicles from early endosomes to lysosomes, with no quench or wash required.
-Reactive oxygen species: Cells that are environmentally stressed usually contain greatly increased levels of reactive oxygen species (ROS). CellROX reagents are fluorogenic probes developed for the detection and quantitation of ROS in live cells. These cell-permeant reagents are non-fluorescent or very weakly fluorescent in the reduced state; however, when oxidized, they become brightly fluorescent and remain localized within the cell. We offer CellROX Green (Cat. No. C10492), CellROX Orange (Cat. No. C10493), and CellROX Deep Red (Cat. No. C10491) Assay Kits validated for flow cytometry.

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

引用および参考文献 (129)

引用および参考文献
Abstract
Normal fertilization occurs with eggs lacking the integrin alpha6beta1 and is CD9-dependent.
Authors:Miller BJ, Georges-Labouesse E, Primakoff P, Myles DG
Journal:J Cell Biol
PubMed ID:10851025
'Previous results, based on inhibition of fertilization by an anti-alpha6 integrin mAb (GoH3), suggest that the alpha6beta1 integrin on mouse eggs functions as the receptor for sperm (Almeida, E.A., A.P. Huovila, A.E. Sutherland, L.E. Stephens, P.G. Calarco, L. M. Shaw, A.M. Mercurio, A. Sonnenberg, P. Primakoff, D.G. Myles, and J.M. ... More
Acetylcholine-induced calcium signaling and contraction of airway smooth muscle cells in lung slices.
Authors:Bergner A, Sanderson MJ
Journal:J Gen Physiol
PubMed ID:11815668
'The Ca(2+) signaling and contractility of airway smooth muscle cells (SMCs) were investigated with confocal microscopy in murine lung slices (approximately 75-microm thick) that maintained the in situ organization of the airways and the contractility of the SMCs for at least 5 d. 10--500 nM acetylcholine (ACH) induced a contraction ... More
Intracellular astrocyte calcium waves in situ increase the frequency of spontaneous AMPA receptor currents in CA1 pyramidal neurons.
Authors:Fiacco TA, McCarthy KD
Journal:J Neurosci
PubMed ID:14736858
'Spontaneous neurotransmitter release and activation of group I metabotropic glutamate receptors (mGluRs) each play a role in the plasticity of neuronal synapses. Astrocytes may contribute to short- and long-term synaptic changes by signaling to neurons via these processes. Spontaneous whole-cell AMPA receptor (AMPAR) currents were recorded in CA1 pyramidal cells ... More
The sources and sequestration of Ca(2+) contributing to neuroeffector Ca(2+) transients in the mouse vas deferens.
Authors:Brain KL, Cuprian AM, Williams DJ, Cunnane TC
Journal:J Physiol
PubMed ID:14500773
'The detection of focal Ca(2+) transients (called neuroeffector Ca(2+) transients, or NCTs) in smooth muscle of the mouse isolated vas deferens has been used to detect the packeted release of ATP from nerve terminal varicosities acting at postjunctional P2X receptors. The present study investigates the sources and sequestration of Ca(2+) ... More
Control of IP(3)-mediated Ca2+ puffs in Xenopus laevis oocytes by the Ca2+-binding protein parvalbumin.
Authors:John LM, Mosquera-Caro M, Camacho P, Lechleiter JD
Journal:J Physiol
PubMed ID:11507154
'1. Elementary events of Ca2+ release (Ca2+ puffs) can be elicited from discrete clusters of inositol 1,4,5 trisphosphate receptors (IP(3)Rs) at low concentrations of IP(3). Ca(2+) puffs have rarely been observed unless elicited by either hormone treatment or introduction of IP(3) into the cell. However, cells appear to have sufficient ... More