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Applications |
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Sensitive
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Detect as little as 20 pg dsDNA per band |
High Contrast
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Bright green fluorescence with exceptionally low background |
Easy to Use
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No destaining or washing steps |
Versatile
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Can be used with many different electrophoresis platforms |
Convenient
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Staining does not interfere with DNA modification enzymes |
Economical
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Less expensive than silver staining |
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Features |
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Sybr Green I and Sybr Green II nucleic acid gel stains are ultra sensitive gel stains that surpass conventional dyes,
including ethidium bromide, by more than an order of magnitude in nucleic acid sensitivity.
SYBR Green stain is extremely versatile and easy to use. It is compatible with many different electrophoresis
platforms, including native and denaturing agarose and polyacrylamide gel electrophoresis, pulsed field gel
electrophoresis and capillary electrophoresis. SYBR Green stain has an exceptionally high affinity for dsDNA,
making it possible to stain dsDNA prior to electrophoresis. Furthermore, SYBR Green stain does not interfere with
many enzymes used in molecular biology, including Taq DNA polymerase, reverse transcriptase, restriction
endonucleases, and T4 DNA ligase. Finally, SYBR Green stain has been shown to be much less mutagenic than ethidium
bromide in Ames tests.
Sybr Green I |
Sybr Green II |
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SYBR Green I nucleic acid gel stain is ideal for detecting double-stranded
DNA (dsDNA) in electrophoretic gels using laser scanners, CCD-based
image documentation systems or standard Polaroid photography. Following
electrophoresis, gels are simply stained in buffered dye solution.
No destaining or wash steps are required.
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SYBR Green II nucleic acid gel stain is ideal for single stranded DNA (ssDNA) and RNA in electrophoretic gels using laser scanners, CCD-based
image documentation systems or standard Polaroid photography. Following
electrophoresis, gels are simply stained in buffered dye solution.
No destaining or wash steps are required.
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Sybr Green stained DNA agarose gel
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Detect rare PCR products - The
superior sensitivity of SYBR Green stain makes it possible to detect
rare amplicons, reduce cycle numbers for PCR and RT PCR and accurately
quantitate low numbers of PCR products made during the linear portion
of the reaction, facilitating high throughput and competitive PCR
analysis.
Save money on DNA typing - SYBR
Green stain is as sensitive as silver staining- but less expensive
- for human identity determination, CAG repeat detection and mtDNA
deletion analysis.
Use fewer cells to visualize apoptosis
ladders - SYBR Green stain gives brighter signals and lower
background than ethidium bromide, making it possible to visualize
DNA ladders from fewer apoptotic cells.
Perform more sensitive telomerase activity
assays - SYBR Green stain is more sensitive than silver staining
for gel-based detection of telomerase activity, allowing simultaneous,
non-isotopic measurement of both enzyme activity and processivity.
Eliminate radioactivity in DNA damage assays
- SYBR Green stain is as sensitive as 3H-labeled thymidine for detecting
DNA damage.
Perform real-time or kinetic PCR analysis
- The presence of SYBR Green stain during PCR does not interfere with
Taq polymerase or reverse transcriptase, and primers contribute little
to the signal, allowing amplification to be monitored in real time.
Detect lower amounts of contaminating DNase
- SYBR Green stain is at least ten times more sensitive than
ethidium bromide for detecting DNase activity using gel-based or radial
diffusion assays.
Detect dsDNA using capillary electrophoresis
- The high affinity for dsDNA and the excellent signal to background
ratio make SYBR Green stain the dye of choice for capillary electrophoresis
studies.
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SYBR® Green I |
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SYBR® Green II |
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Detailed information
Please contact us info@raytest.com; +49 7082 92 55 0
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