SYTO™ Orange Fluorescent Nucleic Acid Stain Sampler Kit - SYTO™ dyes 80-85 - 50 μL each
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Invitrogen™

SYTO™ Orange Fluorescent Nucleic Acid Stain Sampler Kit - SYTO™ dyes 80-85 - 50 μL each

The SYTO Orange Fluorescent Nucleic Acid Stain Sampler Kit contains our collection of cell-permeant, orange-fluorescent SYTO nucleic acid stains. Because深入閱讀
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產品號碼Quantity
S113601 kit
產品號碼 S11360
價格 (HKD)
4,354.00
Each
新增至購物車
Quantity:
1 kit
價格 (HKD)
4,354.00
Each
新增至購物車

The SYTO Orange Fluorescent Nucleic Acid Stain Sampler Kit contains our collection of cell-permeant, orange-fluorescent SYTO nucleic acid stains. Because the dyes may demonstrate different staining behaviors with various tissues and cells, it may be necessary to test the dyes to find the optimal dye for a specific application. The kit contains 50 μL each of SYTO 80–85 dyes.

Any physiological buffer between pH 7.0–8.0, including PBS, can be used to dilute the SYTO dyes for the staining solution.

For Research Use Only. Not for use in diagnostic procedures.
規格
ColorOrange
DescriptionSYTO™ Orange Fluorescent Nucleic Acid Stain Sampler Kit - SYTO™ dyes 80-85, 50 μL each
Detection MethodFluorescence
Dye TypeCell-Permeant
Emission545, 544, 560, 559, 582, 583 nm
Excitation Wavelength Range531, 530, 541, 543, 567, 567 nm
For Use With (Equipment)Fluorescence Microscope
Product LineSYTO
Quantity1 kit
Shipping ConditionRoom Temperature
Volume (Metric)50 μL
Label TypeFluorescent Dye
Product TypeStains Dimer Sampler Kit
SubCellular LocalizationNucleic Acids
Unit SizeEach
內容物與存放
Store in freezer at -5°C to -30°C and protect from light.

常見問答集 (常見問題)

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.

引用資料與參考文獻 (2)

引用資料與參考文獻
Abstract
SYTO probes in the cytometry of tumor cell death.
Authors:Wlodkowic D, Skommer J, Darzynkiewicz Z,
Journal:Cytometry A
PubMed ID:18260152
Apoptosis is a complex and finely controlled cell death process of great relevance in tissue homeostasis and pathogenesis. The majority of classical apoptotic features can be examined by flow as well as image cytometry. Therefore, cytometry has been used as a technology of choice in studies of tumor cell demise. ... More
Synergistic effects of proteasome inhibitor carfilzomib in combination with tyrosine kinase inhibitors in imatinib-sensitive and -resistant chronic myeloid leukemia models.
Authors:
Journal:Oncogenesis
PubMed ID:24590311