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AAT Bioquest

JUN Dye qPCR Calibration Solution *10,000X*

ABI 7500 FAST system JUN dye spectrum.
ABI 7500 FAST system JUN dye spectrum.
ABI 7500 FAST system JUN dye spectrum.
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Physical properties
SolventWater
Spectral properties
Extinction coefficient (cm -1 M -1)1100001
Excitation (nm)610
Emission (nm)628
Quantum yield0.851
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC12171501

OverviewpdfSDSpdfProtocol


Extinction coefficient (cm -1 M -1)
1100001
Excitation (nm)
610
Emission (nm)
628
Quantum yield
0.851
Real-time thermal cyclers require calibration to generate a spectral profile for the fluorescence signal. Since instruments can differ in fluorescence detection sensitivity, the concentrations needed to calibrate any dye, such as JUN, will depend on the device used. The AAT Bioquest JUN dye qPCR Calibration Solution supplied as a 10,000X concentrate is compatible with a wide variety of qPCR instruments, including the ABI7500 Fast, QuantStudio™, and ViiA™ 7 systems. Calibration and verification should be run every six months or as needed. Please refer to the instrument maintenance guide for complete instructions on use.

Platform


qPCR

Recommended platePCR Microplate
Instrument specification(s)JUN Filter

Example protocol


SAMPLE EXPERIMENTAL PROTOCOL

This generic protocol is suitable for the ABI7500 FAST qPCR instrument. For complete instructions on use, refer to the maintenance guide for your instrument.

Prepare a JUN calibration plate:
  1. Prepare a JUN Dye qPCR Calibration working solution by mixing 1 µL of the 10,000X JUN Dye qPCR Calibration Solution with 10 mL of nuclease-free water or qPCR buffer.

    Note: The final dye concentration must be optimized based on the calibration requirements for your instrument. Refer to the manufacturer’s maintenance guide for detailed instructions.

  2. Add 20 µL of the JUN Dye qPCR Calibration working solution to all wells of a reaction plate.

    Note: The volume may vary depending on your instrument. Refer to the manufacturer’s maintenance guide for detailed instructions.

  3. Seal the plate with an optical adhesive cover.

  4. Centrifuge the plate for 2 minutes at < 1500 rpm.

  5. Check that the liquid in each well of the plate is at the bottom of the well. If not, centrifuge the plate again at a slightly higher rpm and for a longer period of time.

  6. For complete calibration instructions, refer to the maintenance guide for your instrument.

Spectrum


Open in Advanced Spectrum Viewer
spectrum

Spectral properties

Extinction coefficient (cm -1 M -1)1100001
Excitation (nm)610
Emission (nm)628
Quantum yield0.851

Images


References


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An Efficient Probe-Based Quantitative PCR Assay Targeting Human-Specific DNA in ST6GALNAC3 for the Quantification of Human Cells in Preclinical Animal Models.
Authors: Ren, Jinfeng and Liu, Ke and Hu, Lang and Yang, Ruoning and Liu, Yuting and Wang, Siyu and Chen, Xinzhu and Zhao, Shuli and Jing, Luyao and Liu, Tiantian and Hu, Bin and Zhang, Xuefeng and Wang, Hui and Li, Hui
Journal: Molecular biotechnology (2024)
Internationally standardized respiratory viral load testing with limited resources: A derivative-of-care calibration strategy for SARS-CoV-2.
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