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Applied Biosystems™ Sequencing Standard, BigDye™ Terminator v1.1, for 3500/SeqStudio™ Flex
Description
Includes
Kit contains four tubes of DNA of a known 1200 base pair sequence prepared with BigDye® Terminator v1.1. Each tube can perform one spectral calibration/performance check and/or one control sequencing run on the Applied Biosystems 3500 and SeqStudio Flex series genetic analyzers.
The BigDye Terminator v1.1 sequencing standard kit contains four tubes, each of which contains enough DNA of a known 1200 base pair sequence prepared with BigDye Terminator v1.1 to perform one spectral calibration⁄performance check and/or one control sequencing run on the Applied Biosystems 3500 and SeqStudio Flex series genetic analyzers. The DNA contained in the preparation has been lyophilized to maximize stability.
Order Info
4 Tubes
Specifications
Specifications
| Content And Storage | This kit contains four tubes of DNA of a known 1200 base pair sequence prepared with BigDye Terminator v1.1. Each tube can perform one spectral calibration⁄performance check and⁄or one control sequencing run on Applied Biosystems 3500 or SeqStudio Flex series genetic analyzers. Store kit at -15 to -25°C. |
| Sample Type | DNA |
| For Use With (Equipment) | 3500 Series Genetic Analyzers, SeqStudio Flex Series Genetic Analyzers |
| For Use With (Application) | Sequencing |
| Label or Dye | ROX, TAMRA™, Rhodamine 110, Rhodamine 6G |
| Product Line | BigDye Terminator, BigDye |
| Product Type | Sequencing Standards |
| Quantity | 4 Tubes |
| Shipping Condition | Dry Ice |
Frequently Asked Questions (FAQs)
Some of the causes of another sequence appearing under the primary sequence are:
• Contamination: There is more than one species of DNA present (e.g., multiple PCR products).
• Primers: Primer is annealing in more than one location on the template, primer dimer, primer degradation or not manufactured properly resulting in N+1 or N-1, carry over from PCR reaction, or primers pairs in a multiplex reaction that are not appropriate for multiplexing (i.e., primers anneal inappropriately).
• Spectral/Matrix: If the raw data signal intensity of the sample is too high or saturated it can exceed the amount of color bleedthrough (or spectral overlap) that the matrix (310) or spectral (3130, 3730, 3500) are removing, resulting in secondary peaks appearing in a very specific pattern (e.g., a red peak always appearing under a green peak). A change in the camera, laser, or optical alignment requires that a new matrix be made or a new spectral calibration be performed.
For more information on more than one sequence or set of peaks in a sequencing run, please refer to the DNA Sequencing by Capillary Electrophoresis: Applied Biosystems Chemistry Guide: Second Edition (Cat. No. 4305080, Rev. C). The guide can be found by searching the Thermo Fisher Scientific website with the catalog number 4305080.
The sequencing standard has a shelf life of one year from the date of shipment, unless otherwise listed on the CofA. Our Terms and Conditions of sale can be found here(https://www.thermofisher.com/content/dam/LifeTech/Documents/PDFs/Terms-and-Conditions-of-Sale.pdf).
The sequencing standard is intended to be used after resuspension in Hi‑Di Formamide. It can be injected multiple times; the number of times will vary depending on the instrument-specific standard used. This information can be found in the product insert. The sequencing standard should be stable for 24 hours on the instrument.
Some of the other causes of an Unstable Electrophoresis current detected error message are:
1.Leak on the system
2. Polymer that:
-Has expired
-Has been left on the instrument for more than the recommended time
-Is a mixture of expired polymer and non-expired polymer
3. Running Buffer that was:
-On the instrument longer than 2 weeks
-Not filled to the fill line or evaporated below the fill line
4. An arcing event that was not cleaned afterwards using the water wash wizard
5. Not performing regular maintenance on the instrument
6. Hardware issues
Inspect the system for leaks. If you do not see any leaks on the system, perform the wash the pump chamber and channels wizard using the conditioning pouch and place fresh, non-expired polymer and fresh Anode and Cathode buffer containers. If the problem persists, a service call may be required.
If the instrument is not in use, it is not necessary to replace the buffer every 14 days. However, the buffer level needs to remain at the fill line to prevent the capillary or array from drying out. Top off the buffer volume with water if necessary. Replace the anode and cathode buffer containers prior to starting a new run.
For Research Use Only. Not for use in diagnostic procedures.