DNA Loading buffer I Fluoro (6x)

Fluorescence Ex/Em spectra of DNA loading buffer I Fluoro bound to DNA


Order number: M3323.0001

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Loading buffer I Fluoro is a fluorescent reagent that produces instant visualization of DNA... more
Product information "DNA Loading buffer I Fluoro (6x)"

Loading buffer I Fluoro is a fluorescent reagent that produces instant visualization of DNA bands upon blue light or UV illumination of agarose gels. Supplied in 6X DNA Loading Buffer, Loading buffer I Fluoro is used to prepare DNA markers or samples for loading on agarose or polyacrylamide gels. 

Loading buffer I Fluoro is the sensitive staining reagent available for detecting the double-stranded DNA (dsDNA). It contains three tracking dyes (bromophenol blue, xylene cyanol FF, and orange G) for visually tracking the DNA migration during the electrophoresis plus an additional fluorescence dye for detection of DNA bands without an additional staining of the gel. It is an ideal alternative to Ethidium Bromide (EtBr).

Approximate fluorescence excitation / emission: 300, 495 / 537 nm, bound to nucleic acid.

For more information on our SimplyEnlight PCR products, read our blog now. Genaxxon's SimplyEnlight PCR - Unlock the Power of Your PCR!

Picture 1: Comparison of UV- and blue light excitation             Picture 2: Effect of EtBr plus UV on cloning efficiency.

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Our comment on "DNA Loading buffer I Fluoro (6x)"
◈ Sensitivity – High sensitivity at least as Ethidium Bromide. ◈ Convenience – Ready to Use. Same application procedures as the 6X Loading Dye. ◈ Time efficiency – No staining requirement. No de-staining requirement. Low background value. Imaging directly during or after electrophoresis possible. ◈ Compatibility – Use of blue light or UV for detection. ◈ Economic – No expenses required for waste management.
Specifications: 6-time loading buffer for agarose gels contains: Glycerin, EDTA, Bromophenol... more
 

Technical Data:

Specifications:
6-time loading buffer for agarose gels
contains: Glycerin, EDTA, Bromophenol blue, Xyclene cyanol, Orange G plus a fluorescence dye

application:

for application of DNA onto Agarose and Polyacrylamide gels

Source

synthetic

Sicherheits Hinweise / Safety

Klassifizierungen / Classification

eclass-Nr: 32-16-05-02
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Dokumente - Protokolle - Downloads

Here you will find information and further literature on DNA Loading buffer I Fluoro (6x). For further documents (certificates with additional lot numbers, safety data sheets in other languages, further product information) please contact Genaxxon biosience at: info@genaxxon.com or phone: +49 731 3608 123.

 
 
 
FAQ
Fragen & Antworten zum Artikel ... mehr
Is the integrated fluorescent dye non-toxic?
Yes, the integrated fluorescent dye DNA loading buffer I Fluoro (6x) is a non-toxic nucleic acid dye. It can be easily disposed of with normal waste. Separate handling of the waste as with EtBr is therefore not necessary. If necessary, obtain information from your local waste disposal company.
Is it necessary to use the GenLadder 100 bp Plus with gel staining dye when using the Red MasterMix Fluoro (2X)?
If you want to benefit from all the advantages of the SimplyEnlight PCR products, you will also need to use a DNA ladder with fluorescent dye to avoid further staining of the gel. To make it as convenient as possible for you, you can use our GenLadder 100bp Plus with staining dye for this purpose. However, you can take our DNA Ladder 100bp (or any other) and add our DNA Loading Buffer I Fluoro (6X) in a 5:1 ratio before loading the gel.
Can I use my own cycling conditions when using the Red MasterMix Fluoro (2X)?
Yes, you can use your own cycling conditions. Please note that the cycling conditions in our protocol are only guidelines for PCR amplification. Optimal reaction conditions such as incubation times, temperatures, and amount of template DNA may vary and must be determined individually. Besides this, optimization of the annealing temperature is important to guarantee an optimal amplification. We recommend performing a temperature gradient and using primers with a Tm >60°C (Tm = melting temperature of the primer, which is the temperature at which 50% of the primer bind to the complementary sequence of the target DNA.)
I have observed a migration shift in the gel electrophoresis using the SimplyEnlight PCR products. What should I do?
If DNA concentration is less than 4pg, it may cause a migratory shift when performing gel electrophoresis. To remedy this, we recommend removing the fluorescent dye prior to post-staining with our DNA Loading buffer I Fluoro (6x) again for restoring the DNA molecular weight in the original position. To remove the fluorescent dye, immerse the PCR product containing the fluorescent dye into 100mM NaCl and add 2.5 volumes of absolute or 95% ethanol. Incubate on ice for 20 min and centrifuge the mixture at 4°C for at least 10 minutes. Then remove the suspension of ethanol and wash the pellet with 1mL of 70% ethanol. Dry the residual ethanol and resuspend the dsDNA in the TE buffer.