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JademiRNA™ Mix-iCycler

2X QPCR Master Mix
Catalog #: M1118
$360.00

Product Details

Cat # +Size M1118-500
Size 4 x 1.25 ml
Highlights 2X QPCR Master Mix
Storage Conditions -20°C
Shipping Conditions Dry Ice
USAGE For Research Use Only! Not For Use in Humans.

Details

2X QPCR Master Mix


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BioVision aims to provide our customers innovative tools for accelerating drug discovery and biological research. BioVision offers >8,000 products including the most comprehensive array of assay kits for key targets in Metabolic pathways.
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What is the difference between Jade™ Master Mixes (BV Cat# M1105-M1120) and SybrGreen? Which one has better features? What is the dye used in Jade™ Master Mix?
Jade™ Master Mixes include a new generation of SybrGreen dyes, which give a stronger signal when bound to dsDNA as compared to SybrGreen. They also have reduced toxicity. Jade™ Master Mixes provide much higher sensitivity and better low-copy detection results. Please click the link https://www.biovision.com/documentation/support/FAQ-QPCR.pdf for more FAQs on QPCR Master mixes.
What are the main advantages of JadeTM Master Mixes?
JadeTM Master Mixes (BV Cat# M1105-M1120) provide high sensitivity in a ready-to-use format. Additionally, BioVision’s QPCR Master Mix formulations are optimized for different QPCR instruments available in the market.
Usually a SYBR dye doesn’t require calibration. Does JadeTM Master Mixes require calibration?
JadeTM Master Mixes do not require calibration.
Are Jade™ Master Mixes suitable for experiments being setup under normal lighting?
Jade Master Mixes™ are very stable and are suitable for setting up experiments under normal lighting.
What are JademiRNA™ Master Mixes?
Jade miRNA™ Master Mixes are designed specifically for quantitative real-time analysis of miRNA obtained from RNA samples. The Master Mix is also designed to eliminate primer-dimer formation and amplification of premature miRNAs. The chemically modified Hot Start Taq polymerase included in the Master Mix significantly reduces the non-specific PCR amplification observed with regular Taq polymerases.