WebLow concentrations are a possible cause for low 260/230 ratios. Thermo says they can measure up to 2 ng/uL, but I wouldn't rely on that. Although this wouldn't explain these ratios for your higher concentrated sample. Could you increase your concentration by lowering the elution volume or doing multiple elution steps? Micromoronics • 3 yr. ago Webrespective 260/280 values. Expected 260/230 values are commonly in the range of 2.0-2.2. If the ratio is appreciably lower than expected, it may indicate the presence of contaminants which absorb at 230 nm. Typical spectral pattern for Nucleic Acid (Figure 1) Figure 1. EDTA (Figure 2), carbohydrates and phenol all have absorbance near 230 nm.
260/280 and 260/230 Ratios NanoDrop ND-1000 and ND-8000 8 …
Web23 de ago. de 2008 · In a broad sense, >2.0 values suggest that your nucleic acid sample is generally not degraded. The nasty caveat is that this gives you no possible way of excluding the possibility that there is DNA contamination in your RNA. You could try running it on an Agilent Bioanalyzer RNA chip or run an agarose gel to do a further QC check. Webrespective 260/280 values. Expected 260/230 values are commonly in the range of 2.0-2.2. If the ratio is appreciably lower than expected, it may indicate the presence of … oracle and cloud
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Web19 de fev. de 2013 · The 260/230 ratio gives you idea about the contaminants in your sample. Guanidine isothiocyanate, which is usually used for RNA isolation, absorbs at … Web4 de fev. de 2024 · 260/230 Ratio The ratio of absorbance at 260 and 230 nm can be used as a secondary measure of DNA or RNA purity. In this case, a ratio between 2.0 - 2.2 is … http://www.protocol-online.org/biology-forums/posts/39027.html oracle and competitors