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Transfer SKU GLYCO BLUE COPRECIP 5 X 300UL 15MG/ML,AM9516,赛默飞世尔

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订货号 9MJ9302
品牌型号 赛默飞世尔 AM9516
货期 询货期
最小订货量 1套
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产品介绍 Product Description
规格
Chemical Name or Material: Glycogen
Form: Liquid
Product Line: Ambion™, GlycoBlue™
Purity or Quality Grade: Molecular Biology Grade
Quantity: 5 x 300μL
Shipping Condition: Dry Ice
储存
Store at –20°C.
描述

GlycoBlue™ Coprecipitant consists of a blue dye covalently linked to glycogen, a branched chain carbohydrate, which is useful as a nucleic acid coprecipitant. The attached dye increases visibility of the pellet. This product is an ideal coprecipitant in nuclease protection assays at 1/100 dilution of stock solution.

Features of GlycoBlue™ Coprecipitant:

• Ideal for RT-PCR
• Increases pellet mass and visibility
• Quantitative recovery of low concentrations (ng/mL) of nucleic acid
• Prevents pellet loss in nuclease protection assays

What is a coprecipitant?
Coprecipitants are inert substances used to aid recovery of nucleic acids during alcohol precipitations. While they can be used for precipitating large amounts of nucleic acids, they are essential for quantitative recovery of small amounts of nucleic acids in dilute solutions. Often, the use of such molecules is desirable for no other reason but visualization of the pelleted precipitate after centrifugation. GlycoBlue™ Coprecipitant can be added to nucleic acid solutions at a final concentration of 50–150 µg/mL. When a typical acetate/alcohol precipitation is done, the GlycoBlue™ Coprecipitant will precipitate with the nucleic acids, facilitating good RNA or DNA recovery while increasing the size and visibility of the pellet. Since glycogen does not contain appreciable amounts of nucleic acids, it is often preferable to yeast RNA as a coprecipitant, especially in applications where nucleic acid mass is being assessed or where added nucleic acid could interfere or compete with subsequent enzymatic reactions. The glycogen used is isolated from mussel, a biological source, as are most other preparations of this coprecipitant. Glycogen is treated with Proteinase K and SDS to remove any contaminating nucleases, and then phenol/chloroform extracted, ethanol precipitated, and resuspended in nuclease-free water. The glycogen is guaranteed RNase- and DNase-free.

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