FxCycle™ PI/RNase Staining Solution
FxCycle™ PI/RNase Staining Solution
Invitrogen™

FxCycle™ PI/RNase Staining Solution

FxCycle™ PI/RNase染色液は、固定細胞中のDNA含有量のフローサイトメトリー解析に使用されます。一般的な赤色蛍光染色剤であるヨウ化プロピジウム(PI)は、配列の優先度がほとんど、またはまったくなく、DNAの4–5塩基対あたり1つの色素の化学量論量の塩基間に挿入することによってDNAに結合します。PIはRNAにも結合するため詳細を見る
製品番号(カタログ番号)数量
F10797200反応
製品番号(カタログ番号) F10797
価格(JPY)
31,100
Each
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数量:
200反応
FxCycle™ PI/RNase染色液は、固定細胞中のDNA含有量のフローサイトメトリー解析に使用されます。一般的な赤色蛍光染色剤であるヨウ化プロピジウム(PI)は、配列の優先度がほとんど、またはまったくなく、DNAの4–5塩基対あたり1つの色素の化学量論量の塩基間に挿入することによってDNAに結合します。PIはRNAにも結合するため、RNAとDNAの染色を区別するためにRNaseによる処理が必要です。このヨウ化プロピジウム溶液には、DNaseフリーのRNase Aと透過化試薬が含まれます。すぐに使用できます:固定細胞に染色液を添加し、インキュベートするだけで、洗浄することなくフローサイトメーターで取得できます。

フローサイトメトリーにおける固定細胞および生細胞の細胞周期解析に関連するすべての製品の選択ガイドをご覧ください。
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
染色剤タイプヨウ化プロピジウム
励起波長域535⁄617
使用対象 (装置)フローサイトメーター
形状溶液
フォーマットチューブ
製品ラインFxCycle
数量200反応
出荷条件室温
製品タイプ染色液
SubCellular Localization
Unit SizeEach
組成および保存条件
FxCycle™ PI/RNase染色液1本(100 mL)。室温で保管し、遮光します。室温で保管してください

よくあるご質問(FAQ)

My cell cycle data show a single peak, not a proper cell cycle profile. How can I fix this?

There are several factors that contribute to the quality of the cell cycle profile. Cell number, dye concentration, incubation temperature, incubation time, flow rate (on a traditional flow cytometer utilizing hydrodynamic focusing), total number of cells acquired, elimination of dead cells, and removal of aggregates from data analysis should all be considered when analyzing the cell cycle.

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

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.