SYTOX™ Blue Nucleic Acid Stain - 5 mM Solution in DMSO

Citations & References (27)

Invitrogen™

SYTOX™ Blue Nucleic Acid Stain - 5 mM Solution in DMSO

SYTOX™青色核酸染色剤は、生細胞には浸透しない優れた青色蛍光核および染色体対比染色剤であり、集団内の死細胞の有用なインジケーターとなります。DNAに結合した色素の励起／発光極大は444/480 nmです。詳細を見る

製品番号（カタログ番号）	数量
S11348	250 μL

製品番号（カタログ番号） S11348

価格（JPY）

74,100

お問い合わせください ›

250 μL

SYTOX™青色核酸染色剤は、生細胞には浸透しない優れた青色蛍光核および染色体対比染色剤であり、集団内の死細胞の有用なインジケーターとなります。DNAに結合した色素の励起／発光極大は444/480 nmです。

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。

色Blue

検出法蛍光

染色剤タイプ細胞透過性

発光480 nm

励起波長域444⁄480

使用対象 (装置)フローサイトメーター

フォーマットチューブ

製品ラインSYTOX

数量250 μL

出荷条件室温

容量（メートル法）250 μL

標識タイプFluorescent Dye

製品タイプ核酸染色

SubCellular Localization核、核酸

Unit SizeEach

組成および保存条件

SYTOX™青色核酸染色液（DMSO中の5 mM溶液）のバイアルが1つ含まれています。フリーザー（-5～-30°C）で保管、乾燥した状態で、光から保護してください。

よくあるご質問（FAQ）

How do SYTO dyes bind to DNA?

The binding mode of SYTO nucleic acid stains is unknown. However, the behavior of these and related nucleic acid dyes suggests the following binding properties:

1.They appear to contact the solvent (suggested by sensitivity to salt, divalent cations, and in particular, SDS) and thus are likely to have contacts in the grooves.
2.All SYTO dyes appear to show some base selectivity and are thus likely to have minor groove contacts.
3.They can be removed from nucleic acid via ethanol precipitation; this characteristic is not shared by ethidium bromide and other intercalators. Likewise, the dyes are not removed from nucleic acid via butanol or chloroform extraction. These extraction methods do remove ethidium bromide from nucleic acid. 4. SYTO binding is not affected by nonionic detergents.
5. SYTO dyes are not quenched by BrdU, so they do not bind nucleic acids in precisely the same way as Hoechst 33342 and DAPI ((4′,6-diamidino-2-phenylindole).

SYBR Green I has shown little mutagenicity on frameshift indicator strains, indicating that it isn't likely to strongly intercalate.

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

I am using SYTOX AAdvanced as a dead cell stain, but all of my cells are labeling even though I am certain that they are supposed to be alive. These are adherent cells that I have trypsinized. Why am I getting false-dead signals?

SYTOX AAdvanced labels only dead cells because it is a cell impermeant dye. The dye can only enter cells that have a compromised plasma membrane. Trypsinization may cause temporary disruption of the plasma membrane, sufficient to allow staining with a cell impermeant dye. You can reduce the “false-dead” problem by either reducing the amount of trypsin and/or reduce the incubation time for trypsinization or use a gentler dissociation reagent such as TrypLE Express, TrypLESelect reagents, or Versene. After trypsinization, wash well, and if possible, allow a recovery time in normal culture media before staining with any of the SYTOX dyes.

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

How long can I leave SYTOX Blue Nucleic Acid Stain - 5 mM Solution in DMSO on my cells during imaging?

SYTOX dyes are only tested for end-point assays, not for leaving in cell solutions long term. Therefore, we do not recommend using SYTOX Blue Nucleic Acid Stain - 5 mM Solution in DMSO for long-term imaging.

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

引用および参考文献 (27)

引用および参考文献

Abstract

Signaling at the gliovascular interface.

Authors:Simard M, Arcuino G, Takano T, Liu QS, Nedergaard M

Journal:J Neurosci

PubMed ID:14534260

'Advances in fluorescent calcium indicating dyes over the past decade have identified calcium signaling as the tool by which astrocytes communicate among themselves and with neighboring neurons. Studies of astrocyte-neuron interactions have shown that calcium signaling is a potent modulator of the strength of both excitatory and inhibitory synapses. The ... More

Phosphatidylserine-dependent engulfment by macrophages of nuclei from erythroid precursor cells.

Authors:Yoshida H, Kawane K, Koike M, Mori Y, Uchiyama Y, Nagata S

Journal:Nature

PubMed ID:16193055

'Definitive erythropoiesis usually occurs in the bone marrow or fetal liver, where erythroblasts are associated with a central macrophage in anatomical units called ''blood islands''. Late in erythropoiesis, nuclei are expelled from the erythroid precursor cells and engulfed by the macrophages in the blood island. Here we show that the ... More

Trogocytosis by Entamoeba histolytica contributes to cell killing and tissue invasion.

Authors:Ralston KS, Solga MD, Mackey-Lawrence NM, Somlata, Bhattacharya A, Petri WA,

Journal:

PubMed ID:24717428

'Entamoeba histolytica is the causative agent of amoebiasis, a potentially fatal diarrhoeal disease in the developing world. The parasite was named '

Delivery of macromolecules into live cells by simple co-incubation with a peptide.

Authors:Lee YJ, Erazo-Oliveras A, Pellois JP,

Journal:Chembiochem

PubMed ID:20029930

'n this report, we test the hypothesis that optimized cell-penetrating peptides (CPPs) might deliver macromolecules to the cytosol of live cells by simple co-incubation and without the requirement for any type of conjugation, whether covalent or noncovalent. This hypothesis is based on the observation that the binding of TAT and ... More

Assessment of fluorochromes for two-photon laser scanning microscopy of biofilms.

Authors:Neu TR, Kuhlicke U, Lawrence JR

Journal:Appl Environ Microbiol

PubMed ID:11823234

A major limitation for the use of two-proton laser scanning microscopy (2P-LSM) in biofilm and other studies is the lack of a thorough understanding of the excitation-emission responses of potential fluorochromes. In order to use 2P-LSM, the utility of various fluorochromes and probes specific for a range of biofilm constituents ... More

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