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Protein dye reagent for protein quantification after Bradford (1). • Precise, reproducible and inexpensive • Fast, only five minutes incubation before reading the sample at 595 nm • Suitable for micro (1 - 25 µg protein/ml) and standard (100 – 1000 µg protein/ml) assays50 ml Bradford reagent are sufficient for more than 200 micro assays (1-ml cuvette) or for more than 900 assays in micro titer plates. Protein dye reagent for protein quantification after Bradford (1). • Precise, reproducible and inexpensive • Fast, only five minutes incubation before reading the sample at 595 nm • Suitable for micro (1 - 25 µg protein/ml) and standard (100 – 1000 µg protein/ml) assays50 ml Bradford reagent are sufficient for more than 200 micro assays (1-ml cuvette) or for more than 900 assays in micro titer plates.
Product Detail
Protein dye reagent for protein quantification after Bradford (1). • Precise, reproducible and inexpensive • Fast, only five minutes incubation before reading the sample at 595 nm • Suitable for micro (1 - 25 µg protein/ml) and standard (100 – 1000 µg protein/ml) assays50 ml Bradford reagent are sufficient for more than 200 micro assays (1-ml cuvette) or for more than 900 assays in micro titer plates. Protein dye reagent for protein quantification after Bradford (1). • Precise, reproducible and inexpensive • Fast, only five minutes incubation before reading the sample at 595 nm • Suitable for micro (1 - 25 µg protein/ml) and standard (100 – 1000 µg protein/ml) assays50 ml Bradford reagent are sufficient for more than 200 micro assays (1-ml cuvette) or for more than 900 assays in micro titer plates.
Product Detail
The assay bases on the bichinchoninic acid method (1). Proteins reduce alkaline Cu(II) to Cu(I). Bichinchoninic acid forms a purple complex with Cu(I) with an absorbance maximum at 562 nm. The absorbance is directly proportional to protein concentration. • Fast and sensitive assay: linear detection range from 25 – 1000 µg protein/ml • Easy to use: contains ready-to-use reagents and protein standard • Compatible with many detergents • Less binding variation between different proteins than Bradford assay The assay bases on the bichinchoninic acid method (1). Proteins reduce alkaline Cu(II) to Cu(I). Bichinchoninic acid forms a purple complex with Cu(I) with an absorbance maximum at 562 nm. The absorbance is directly proportional to protein concentration. • Fast and sensitive assay: linear detection range from 25 – 1000 µg protein/ml • Easy to use: contains ready-to-use reagents and protein standard • Compatible with many detergents • Less binding variation between different proteins than Bradford assay
Product Detail
The assay bases on the bichinchoninic acid method (1). Proteins reduce alkaline Cu(II) to Cu(I). Bichinchoninic acid forms a purple complex with Cu(I) with an absorbance maximum at 562 nm. The absorbance is directly proportional to protein concentration. • Fast and sensitive assay: linear detection range from 25 – 1000 µg protein/ml • Easy to use: contains ready-to-use reagents and protein standard • Compatible with many detergents • Less binding variation between different proteins than Bradford assay The assay bases on the bichinchoninic acid method (1). Proteins reduce alkaline Cu(II) to Cu(I). Bichinchoninic acid forms a purple complex with Cu(I) with an absorbance maximum at 562 nm. The absorbance is directly proportional to protein concentration. • Fast and sensitive assay: linear detection range from 25 – 1000 µg protein/ml • Easy to use: contains ready-to-use reagents and protein standard • Compatible with many detergents • Less binding variation between different proteins than Bradford assay
Product Detail
Protein dye reagent for protein quantification after Bradford (1). • Precise, reproducible and inexpensive • Fast, only five minutes incubation before reading the sample at 595 nm • Suitable for micro (1 - 25 µg protein/ml) and standard (100 – 1000 µg protein/ml) assays50 ml Bradford reagent are sufficient for more than 200 micro assays (1-ml cuvette) or for more than 900 assays in micro titer plates. Protein dye reagent for protein quantification after Bradford (1). • Precise, reproducible and inexpensive • Fast, only five minutes incubation before reading the sample at 595 nm • Suitable for micro (1 - 25 µg protein/ml) and standard (100 – 1000 µg protein/ml) assays50 ml Bradford reagent are sufficient for more than 200 micro assays (1-ml cuvette) or for more than 900 assays in micro titer plates.
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© 2026 Copyright. All Rights Reserved.
