Safe-Red™
Cat. No.
G108-R
Unit
1.0 ml
Price
$52.00
| Cat. No. | G108-R |
| Name | Safe-Red™ |
| Unit | 1.0 ml |
| Category | Gel Documentation |
| Description |
abm’s Safe-Red™ is a safe, improved formulation of nucleic acid stain for agarose gel electrophoresis. Safe-Red™ is offered in a convenient, one-step 6X loading dye format that allows for the elimination of toxic Ethidium Bromide and its associated contamination risks with glassware, gel apparatus and environment. Features:
|
| Safeview Series | Loading Dye |
| LED Viewer Compatibility | Yes |
| Stain Color | Red |
| Application |
Safe Detection of dsDNA, ssDNA and RNA in agarose gels. |
| Concentration | 6X |
| Shipping Conditions |
Shipped on blue ice packs. |
| Storage Condition |
Store at 18-25°C. |
| Note |
Dispose of SafeView DNA Stains as you would any other non-carcinogenic fluorescent dye (eg. Acridine orange; Propidium iodide). |
| Material Citation | If use of this material results in a scientific publication, please cite the material in the following manner: Applied Biological Materials Inc, Cat. No. G108-R |
Datasheet
| Can SafeView products be used in replacement of ethidium bromide? | |
|
All SafeView™ products (Safe-Green™, Safe-Red™, SafeView™ Classic, Safe-Red™ Gel) can be used as a complete replacement for your ethidium bromide workflow. |
| How do SafeView products work and why are they not carcinogenic? | |
|
SafeView™ products contain fluorescent compounds that have a strong affinity to nucleic acids. Once bound to a nucleic acid, the compound fluoresces under specific wavelength of light which can then be visualized using a standard UV/Blue light imager. There may be some unknown effects of SafeView™ products that have not been documented in literature but these would also apply to equivalent popular products such as SYBRSafe. However, SafeView™ products are not as carcinogenic as ethidium bromide. |
| How do I use SafeView products? | |
|
Safe-Red™ and Safe-Green™ are supplied in a 6X loading dye format: mix samples and DNA marker with Safe-Red™ or Safe-Green™ at a 1:5 (dye : sample) dilution ratio, and load onto an unstained gel. |
| Can SafeView products differentiate between double stranded and single stranded nucleic acids? | |
|
No, our SafeView products will bind to both double-stranded and single-stranded nucleic acids, albeit with lesser efficiency for single-stranded nucleic acid species.
|
| At what temperature do I store SafeView products? | |
|
SafeView Classic™, Safe-Red™ and Safe-Red™ Gel should be stored at 18-25°C. Safe-Green™ should be stored at 4°C. |
| How sensitive are SafeView products? | |
|
Safe-Green™: 0.2-0.6 ng DNA per band |
| Can SafeView products be used to post-stain gels? | |
|
Yes, SafeView™ Classic and Safe-Red™ Gel can both be used for either pre-cast or post-stain gels.
|
| Do I need to add any loading dye to my samples prior to running them on a SafeView agarose gel? | |
|
If using Safe-Green™ or Safe-Red™, you will not need to add any additional loading dyes to your samples. If using SafeView™ Classic or Safe-Red™ Gel, you will need to add an appropriate DNA loading dye to your samples in order for samples to properly settle and stay in the wells during electrophoresis. |
| We notice band shifting of our DNA fragments when using Safe-Green. Are there any recommendations that you can give us to minimize this band shifting? | |
|
Band shifting to a certain degree is unavoidable for any nucleic acid stain as most of these fluorescent compounds are large, positively charged molecules. Loading dye format nucleic acid stains, while convenient, may also suffer from more prominent band shifting due to the stain binding and migrating with the sample simultaneously during electrophoresis. Post-staining, while takes longer to complete, may be the optimal choice of nucleic acid stain strategy if band shifting issue is a priority. We have observed band shifting with Safe-Green™ as this issue has been documented in the literature to be an inherent property of the specific fluorescent compound. Alternatively we offer SafeView™ Classic which we have observed to exhibit no band shifting issues. |
| I cannot visualize 100bp and 200bp DNA bands on a 1% SafeView agarose gel. What should I do? | |
|
It is often difficult to detect smaller 100bp and 200bp bands on a 1% gel especially if samples are of low concentration. We recommend visualizing smaller fragments on a higher concentration gel - ideally 2% agarose.
|
| Can I use SafeView products to visualize nucleic acids on a polyacrylamide gel? | |
|
SafeView™ products are designed for use with agarose gels, and are not optimized for polyacrylamide gels. However, SafeView™ Classic and Safe-Red™ Gel can both visualize nucleic acids on polyacrylamide gels (Acrylamide, TBE, APS, TEMED) by post staining method.
|
| Can SafeView products be stored at -20°C? | |
|
No, please store Safe-Green™ at 4°C and SafeView™ Classic, Safe-Red™ and Safe-Red™ Gel at 18-25°C. |
| What is the concentration of SafeView products? | |
|
SafeView™ Classic and Safe-Red™ Gel are supplied at a 10,000X concentration. Safe-Green™ and Safe-Red™ are supplied at a 6X concentration.
|
| What color is the tracking dye of Safe-Green and Safe-Red during electrophoresis? | |
|
Safe-Green™ and Safe-Red™ both contain a dark blue tracking dye that migrates at ~300bp on a 1% agarose gel. Safe-Red™ contains an additional light blue tracking dye that migrates at ~4000bp on a 1% agarose gel.
|
| Can I perform gel extraction and subsequent cloning using SafeView products? | |
|
We recommend using SafeView™ Classic or Safe-Red™ Gel which can both be used for gel extraction of DNA fragments destined for cloning. We have observed no decrease in cloning efficiency in comparison to ethidium bromide.
|
| What type of device or imaging system should be used to visualize SafeView agarose gels? | |
|
We recommend using abm’s SafeViewER™ Imager (Cat.No E1001) which is compatible with all SafeView™ products. Additionally, any imaging system with UV, Blue Light and/or LED should be sufficient.
|
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- Diaz-Balzac, CA et al. "Calbindin-D32k is localized to a subpopulation of neurons in the nervous system of the sea cucumber Holothuria glaberrima (Echinodermata)" PLoS ONE 7 (3):e32689 (2012). DOI: 10.1371/journal.pone.0032689. PubMed: 22412907. Application: PCR Products Viewing.
- Machida, RJ et al. "PCR primers for metazoan nuclear 18S and 28S ribosomal DNA sequences" PLoS ONE 7 (9):e46180 (2012). DOI: 10.1371/journal.pone.0046180. PubMed: 23049971. Application: PCR Products Viewing.
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- Ish-Shalom, S et al. "Analysis of fungal gene expression by Real Time quantitative PCR" Methods Mol. Biol. 638:103-114 (2010). DOI: 10.1007/978-1-60761-611-5_7. PubMed: 20238263. Application: PCR Products Viewing.
- Lam, SW et al. "Rapid, specific and quantitative polymerase chain reaction (PCR) detection of pathogenic protozoa Entamoeba histolytica for drinking water supply" Water Science & Technology: Water Supply 11 (4):418-425 (2011). DOI: 10.2166/ws.2011.057. PubMed: 67657423. Application: PCR Products Viewing.
- Kim, SH et al. "The action of HIF-3a variants on HIF-2a–HIF-1ß heterodimer formation is directly probed in live cells" Exp Cell Res 336(2):329-37 (2015). DOI: 10.1016/j.yexcr.2015.06.017. PubMed: 26160453. Application: PCR Products Viewing.
- Vlasschaert, C et al. "Selection preserves Ubiquitin Specific Protease 4 alternative exon skipping in therian mammals" Sci. Rep. 6:20039 (2016). DOI: https://dx.doi.org/10.1038%2Fsrep20039.
- McCoy, P.. "Hormonally induced defects of DNA damage repair genes: an oncogenic driver of prostate cancer (Doctoral dissertation)" : (2018).
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- Dickhout, . "U" S. Patent Application No. 0038597 A1 : (2019).
- Wang, B., Li, D., Cherkasova, V., Gerasymchuk, M., Narendran, A., Kovalchuk, I., & Kovalchuk, O. (2022). Cannabinol Inhibits Cellular Proliferation, Invasion, and Angiogenesis of Neuroblastoma via Novel miR-34a/tRiMetF31/PFKFB3 Axis. Cancers, 14(8), 1908. https://doi.org/10.3390/cancers14081908
- Wu, T., & Li, G. (2022). An Improved EMSA-based Method to Prioritize Candidate cis-REs for Further Functional Validation. BIO-PROTOCOL, 12(8). https://doi.org/10.21769/bioprotoc.4397
- Ataseven, V. S., Ambarcıoğlu, P., & Doğan, F. (2023). Serum and milk levels of antibodies to bovine viral diarrhoea virus, bovine herpesvirus-1 and -4, and circulation of different bovine herpesvirus-4 genotypes in dairy cattle with clinical mastitis. Journal of Veterinary Research, 67(1), 33–40. https://doi.org/10.2478/jvetres-2023-0010
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