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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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S665584-100T
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100T |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$49.90
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S665584-500T
|
500T |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$194.90
|
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| Storage Temp | Store at -20°C,Avoid repeated freezing and thawing | |||||||
|---|---|---|---|---|---|---|---|---|
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
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| Product Description |
Product content
Product Introduction Super DNA Marker consists of 10 DNA fragments, 10,000bp, 5,000bp, 3,000bp, 2,000bp, 1,500bp, 1,000bp, 750bp, 500bp, 250bp, and 100bp respectively, and it can be directly electrophoresed with 5μl of 1×Loading Buffer. This product is a DNA solution containing 1×Loading Buffer, 5μl of which can be taken for direct electrophoresis, which is very convenient to use; the amount of DNA fragment of 1,000bp in electrophoresis is about 150ng, which shows a bright band, and the amount of DNA in other bands is about 50ng. Pre-experiment Preparation and Important Notes 1. This product can be directly frozen and mixed for use without heating. 2. Please change the electrophoresis buffer and use fresh agarose gel in time to avoid affecting the electrophoresis results. 3. When DNA agarose gel electrophoresis, the purity of the gel has a great influence on the clarity of the DNA bands, so try to use good quality agarose, the recommended gel concentration is 1%-3%, voltage 4-8v/cm. 4. The gel concentration is closely related to the separation performance of DNA fragments. The larger the gel concentration, the better the separation performance of short fragment DNA; conversely, the smaller the gel concentration, the more favorable the separation of long fragment DNA. 5. When used with macromolecular dyes, it is recommended to appropriately reduce the amount of Marker or increase the amount of dye. Usage Take 5 μl into the spiking well of the agarose gel (if the spiking well is wider than 6 mm, the amount of sample must be increased appropriately), and carry out electrophoresis.
1% agarose gel electropherogram (5 μ L) |
| 1. Danhe Wang, Xiaomeng Xu, Tao Qiu, Na Ren, Haiyun Liu, Guoxin Fang, Zhen Liu. (2025) Laser Construction TiOx-Ag heterostructure interface for high sensitive coupling resonance enhanced fluorescence in bacterial nucleic acid amplification sensor chip. SENSORS AND ACTUATORS B-CHEMICAL, 423 (136727). |