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Solar Direct Drive Blood Refrigerator
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GERMANIUM DIOXIDE 99.9% Electronic Grade
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NITRIC ACID 69-71% AR
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ACETYL ACETONE AR
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COPPER (I) CHLORIDE 97% LR
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CESIUM SULFATE 99.5% AR
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MERCURY STANDARD SOLUTION FOR AAS - 1000 µG/mL IN HNO3
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CALCIUM NITRATE TETRAHYDRATE AR
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NESSLER’S REAGENT LR
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FURFURAL FOR SYNTHESIS
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PROPIONIC ANHYDRIDE FOR SYNTHESIS
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Floor Standing Low-Speed-Refrigerated-Centrifuge
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Platform PP-20/3
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PERCHLORIC ACID 1M (1N) STANDARDIZED SOLUTION traceable to NIST
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CADMIUM STANDARD SOLUTION FOR AAS - 1000 µG/mL IN HNO3
Contamination is especially problematic in the highly sensitive PCR technique. Originating from aerosolized fragments, contaminant DNA can lead to cross contamination thus resulting in inaccurate data and as a result misinterpreted analysis.
PDS-250 is ready-to-use solution for eliminating DNA, RNA from surface prior PCR reaction preparation. DNA/RNA is removed within seconds after use. The solution contains a non-alkaline and non-carcinogenic agent. PDS-250 is intended for use at PCR cabinets and laminars (e.g. UVT-S-AR), lab devices – Biomagpure 12, TS-100, pipettors – Assist series piettes, etc.
PDS-250 is effective against amplicon, plasmid, or genomic DNA and RNA from most surfaces with the exception of light or non-ferrous metals (e.g. aluminium, copper, lead, nickel, tin, titanium, zinc etc.).
PDS-250 is ready-to-use for eliminating DNA and RNA from suitable surfaces. Fast and easy decontamination; The use of PDS-250 both before and after PCR analysis is fast, easy and ideal to maintain a clean work area and thereby saves time and expenses.
PDS-250 is heat resistant and stable for several years
Recommended Use: Applicable in research and industry only. Not recommended for clinical applications. Use as directed. PDS-250 should be applied on glass, ceramic, plastic, rubber, steel and precious metal. PDS-250 cannot be used for the cleaning of light or non-ferrous metals. To avoid damage or discoloration, it is recommended to spot test sensitive surfaces prior to use.
| Volume | 250 mL |
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DNA/RNA Decontamination Solution PDS-250
Contamination is especially problematic in the highly sensitive PCR technique. Originating from aerosolized fragments, contaminant DNA can lead to cross contamination thus resulting in inaccurate data and as a result misinterpreted analysis.
