Helixyte Gold (SYBR Gold)

10,000X DMSO Solution

SYBR® Gold (Thermo Fisher Scientific) and Helixyte™ Gold are chemically equivalent, nucleic acid gel stains, with an excitation peak at 496 nm and an emission peak at 539 nm. Helixyte™ Gold can be used to detect nucleic acids in agarose and polyacrylamide gels, with a strong preference for DNA over RNA. It is much more sensitive than ethidium bromide, and it can detect as low as picograms of dsDNA on gels.

Example protocol

AT A GLANCE

Spectral Properties of Helixyte™ Gold
Excitation/Emission: 495/540 nm
Important Helixyte™ Gold nucleic acid gel stain is significantly less mutagenic than ethidium bromide. However, we must caution that no data are available on the mutagenicity or toxicity of Helixyte™ Gold stain in humans. It should be treated as a potential mutagen and used with appropriate care due to the fact that this reagent binds to nucleic acids. The disposing of the stain shall be in compliance with local regulations.
We have found the greatest sensitivity is achieved by post-staining which also eliminates the possibility of dye interference with DNA migration. While the precast protocol is more convenient, some DNA samples may experience migration, it is highly recommended the gel running time does not exceed more than 2 hours. The following protocols are recommended. However, some comparisons might be needed to determine which one better meets your needs.

PREPARATION OF WORKING SOLUTION

Helixyte™ Gold working solution (1X)

Make 1X Helixyte™ Gold working solution by diluting the 10,000X stock reagent into pH 7.5 - 8 buffer (e.g., TAE, TBE or TE, preferably pH 8.0).
Note Staining solutions prepared in water are less stable than those prepared in buffer and must be used within 24 hours to ensure maximal staining sensitivity.
Note In addition, staining solutions prepared in buffers with pH below 7.5 or above 8.0 are less stable and show reduced staining efficacy.

SAMPLE EXPERIMENTAL PROTOCOL

Post-Staining Protocol

Run gels based on your standard protocol.
Place the gel in a suitable polypropylene container. Gently add a sufficient amount of the 1X Helixyte™ Gold working solution to submerge the gel.
Note Do not use a glass container, as it will adsorb much of the dye in the staining solution.
Agitate the gel gently at room temperature for ~30 minutes, protected from the light.
Note The staining solution can be stored in the dark (preferably refrigerated) for a week and reused up to 2 - 3 times.
Image the stained gel with a 254 nm transilluminator or a laser-based gel scanner using a long path green filter, such as a SYBR® filter or GelStar® filter.

Pre-Casting Protocol

Prepare agarose gel solution using your standard protocol.
Add 1X Helixyte™ Gold working solution to the gel and mix thoroughly.
Run gels based on your standard protocol.
Image the stained gel with a 254 nm transilluminator or a laser-based gel scanner using a long path green filter, such as a SYBR® filter or GelStar® filter.

DNA-Staining Before Electrophoresis

Incubate DNA with a 1:1000 to 1:3000 dilution of the dye (in TE, TBE, or TAE) for at least 15 minutes prior to electrophoresis.
Run gels based on your standard protocol.
Image the stained gel with a 254 nm transilluminator, or a laser-based gel scanner using a long path green filter such as a SYBR® filter or GelStar® filter.

Spectrum

Open in Advanced Spectrum Viewer

Alternative formats

Name

Helixyte™ Gold Nucleic Acid Gel Stain *10,000X DMSO Solution*

Product family

Name	Excitation (nm)	Emission (nm)
Helixyte™ Green Nucleic Acid Gel Stain 10,000X DMSO Solution	498	522

References

View all 79 references: Citation Explorer

SYBR green real-time PCR for the detection of all enterovirus-A71 genogroups
Authors: Dubot-Peres A, Tan CY, de Chesse R, Sibounheuang B, Vongsouvath M, Phommasone K, Bessaud M, Gazin C, Thirion L, Phetsouvanh R, Newton PN, de Lamballerie X.
Journal: PLoS One (2014): e89963

Development of loop-mediated isothermal amplification and SYBR green real-time PCR methods for the detection of Citrus yellow mosaic badnavirus in citrus species
Authors: Anthony Johnson AM, Dasgupta I, Sai Gopal DV.
Journal: J Virol Methods (2014): 9

Development of both multiple PCR and real-time SYBR green PCR for the detection of Vibrio cholerae non-O1/O139 serogroups
Authors: Li F, Kan B, Wang D.
Journal: Zhonghua Liu Xing Bing Xue Za Zhi (2014): 66

Detection of Cardamom mosaic virus and Banana bract mosaic virus in cardamom using SYBR Green based reverse transcription-quantitative PCR
Authors: Siljo A, Bhat AI, Biju CN.
Journal: Virusdisease (2014): 137

Comparison of SYBR Green and TaqMan methods in quantitative real-time polymerase chain reaction analysis of four adenosine receptor subtypes
Authors: Tajadini M, Panjehpour M, Javanmard SH.
Journal: Adv Biomed Res (2014): 85

Page updated on September 23, 2024

Ordering information

Price
Unit size
Catalog Number	17595
Quantity

Add to cart

Additional ordering information

Telephone	1-800-990-8053
Fax	1-800-609-2943
Email	sales@aatbio.com
International	See distributors
Bulk request	Inquire
Custom size	Inquire
Technical Support	Contact us
Purchase order	Send to sales@aatbio.com
Shipping	Standard overnight for United States, inquire for international

Request quotation

Physical properties

Molecular weight	749.48
Solvent	DMSO

Spectral properties

Excitation (nm)	496
Emission (nm)	539

Storage, safety and handling

H-phrase	H303, H313, H340
Hazard symbol	T
Intended use	Research Use Only (RUO)
R-phrase	R20, R21, R68
Storage	Freeze (< -15 °C); Minimize light exposure
UNSPSC	41116134