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- Milli-Q
- Milli-Q Academic
- Milli-Q Biocel
- Milli-Q Element
- Milli-Q Gradient
- Milli-RO
- Milli-Q Synthesis
Product Family Information
Purification Packs for Milli-Q Academic, Gradient, Biocel, and SynthesisPurification Packs for Milli-Q Academic, Gradient, Biocel, and Synthesis |
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Millipore's Laboratory Water Systems ConsumablesMillipore has developed laboratory water systems consumables adapted to the different feed water qualities as well as the different applications. |
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Purification Packs and Accessories for Compact SystemsProtect your water quality with genuine Millipore productsA combination of purification media is carefully selected to remove typical contaminants. These packs for Milli-Q systems and Milli-RO systems simply snap in and out for replacement. |
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Elix 20/35/70/100 Water Purification SystemsType 2 analytical-grade waterElix systems are designed to produce up to 4000 L/day of Type 2 analytical-grade water from potable tap feedwater to meet or exceed the relevant standards defined by CLSI, ISO® 3696 / BS 3997 and the European and US Pharmacopoeia. |
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详细描述见链接:http://www.millipore.com/catalogue/item/ZFA10UV01
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文献和实验Membrane Transfer and Crosslinking for RNA
The composition of the transfer buffer is usually a 5X SSC/10 mM NaOH solution. These mildly alkaline conditions shear the RNA into smaller fragments and denature it as it is deposited onto the membrane. A brief protocol for assembly (see Figure 1
Labeling Tubulin and Quantifying Labeling Stoichiometry
must be first uncaged to fluorescein. To do this, dilute the labeled tubulin 1/50 to 1/100 in IB + 2 mM DTT in an eppendorf tube. Put the eppendorf tube on a hand held UV lamp, cover with foil (shiny side down) and expose to long wavelength UV for 30'. Obtain
for staining gels (see Step 41) Universal tubing clamps (5 mm) (Spectrum Laboratories) UV lamp Vortex mixer Water bath set at 37°C METHOD Nuclei Preparation from Tissues and Cells Steps 1-8 describe the purification
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