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If anyone would please be able to point me in the direction of a database or something similar which contains standard curves/absorbance levels for BSA and ovalbumin, as measured using a spectrophotometer at 595nm, with the Bradford Assay?

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Final answer:

To find a database containing standard curves for BSA and ovalbumin using the Bradford Assay at 595nm, researchers should check scientific literature and protein databases or contact suppliers of assay reagents.

Step-by-step explanation:

In the field of biology, measuring the concentration of proteins such as BSA (bovine serum albumin) and ovalbumin using the Bradford Assay is a common application of UV-vis spectroscopy. This biochemistry technique utilizes a colorimetric assay, where the absorbance at 595 nm correlates with protein concentration, creating a standard curve. The Bradford reagent reacts with the protein, notably with arginine residues and aromatic amino acids, leading to a color change that can be quantitatively measured using a spectrophotometer.

When constructing standard curves, researchers prepare a series of known protein concentrations and measure their absorbance at a specific wavelength, such as 595 nm for the Bradford Assay. The resulting data create a plot of absorbance versus concentration, which can then be used to determine the unknown protein concentrations in other samples by comparing their absorbance readings to the standard curve.

For finding databases that contain standard curves or absorbance levels for proteins like BSA and ovalbumin, scientific literature, and protein databases, such as the Protein Information Resource (PIR) or UniProt, may occasionally publish these curves in the context of method validation. Alternatively, suppliers of these proteins or the Bradford reagent may provide typical standard curves as part of their product specification sheets. It's important to note that the creation of a standard curve is usually a preliminary step conducted by researchers according to their specific experimental conditions, and these curves should ideally be generated for each new assay.

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