Mm/Hs MAPK1 control siRNA 5 nmol NM 001038663 NM 002745 NM 011949 NM 138957 This product will be discontinued as of June 30 2021 or until stocks last We recommend Mm/Hs MAPK1 control siRNA 20 nmol Download Safety Data Sheets for QIAGEN product components
GE Vernova is an industry leader in the design and manufacturing of high medium and low voltage instrument transformers With more than 100 years of experience We offer a broad array of standard and high accuracy models for revenue metering and system protection applications
Download Safety Data Sheets for QIAGEN product components 2 MSDS Buffer P1 500 ml CofA QIAGEN
The QIAGEN Multiplex PCR Plus Kit is based on QIAGEN s proprietary multiplex PCR technology and ensures PCR success at the first attempt The preoptimized master mix includes HotStarTaq Plus DNA Polymerase and an innovative PCR buffer system specially developed for multiplex PCR The stringent hot start mechanism provided by HotStarTaq Plus DNA Polymerase and
QIAGEN Plasmid Kits provide efficient purification of up to 10 mg transfection grade plasmid or cosmid DNA through gravity flow anion exchange tips 100 mM NaCl; 10 mM Tris Cl pH For the QIAGEN tip 500 the expected yields are 300 500 µg for high copy plasmids and 100 500 µg for low copy plasmids
Reach out to cooperate with QIAGEN Strategic Partnerships & OEM Contact an OEM expert QuantiNova Probe PCR Kit 100 Cat No / ID 208252 For 100 x 20 µl reactions 1 ml 2x QuantiNova Probe PCR Master Mix 250 µl QN ROX Reference Dye 500 µl QuantiNova Yellow Template Dilution Buffer ml Water
Weight Approx 7 kg Width 150 mm Depth 270 mm Height 280 mm The power supply of the TissueLyser LT is compatible with voltages of 100 240 V Disruption principle High speed shaking of samples in 2 ml microcentrifuge tubes with stainless steel or glass beads Protocol/main application on this intrument Sample preparation/sample
QIAGEN provides stainless steel beads and tungsten carbide beads for use in sample disruption with TissueLyser systems High speed shaking of sample material and a single bead in a Collection Microtube or 2 ml microcentrifuge tube for a few minutes allows rapid and efficient disruption of the sample The 3 mm beads are not compatible with
Can be used at low concentrations 20 mM to inhibit non specific binding and at higher concentrations >100 mM to elute the 6xHis tagged protein from the Ni NTA matrix Other additives NaCl Prevents ionic interactions Up to 2 M can be used at least 300 mM should be used MgCl 2 Up to 4 M CaCl 2 Up to 5 mM Glycerol
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Can be used at low concentrations 20 mM to inhibit non specific binding and at higher concentrations >100 mM to elute the 6xHis tagged protein from the Ni NTA matrix Other additives NaCl Prevents ionic interactions Up to 2 M can be used at least 300 mM should be used MgCl 2 Up to 4 M CaCl 2 Up to 5 mM Glycerol
Can be used at low concentrations 20 mM to inhibit non specific binding and at higher concentrations >100 mM to elute the 6xHis tagged protein from the Ni NTA matrix Other additives NaCl Prevents ionic interactions Up to 2 M can be used at least 300 2
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