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Item number | Size | Datasheet | Manual | SDS | Delivery time | Quantity | Price |
---|---|---|---|---|---|---|---|
ABD-25400 | 200 tests | - |
3 - 8 business days* |
397.00€
|
If you have any questions, please use our Contact Form.
You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
Human serum albumin (HSA) is one of the most important carriers for acidic drugs in human plasma... more
Product information "Amplite(TM) Human Serum Albumin (HSA) Site I Binding Assay Kit"
Human serum albumin (HSA) is one of the most important carriers for acidic drugs in human plasma and has been shown to bind a large number of different compounds in a reversible manner. Several different ligand binding sites have been identified for HSA. Among them, Site I has been identified as one of major drug binding sites. Amplite(TM) Human Serum Albumin (HSA) Site I Binding Assay Kit is a fluorescence-based high throughput assay to determine the small molecule binding towards HSA. This assay is based on a novel fluorescent probe, HSA Blue(TM) S1. It has been characterized to bind to the site 1 of HSA with unique spectroscopic and binding properties. HSA Blue(TM) S1 displays a large fluorescence intensity difference between the protein-bound and protein-unbound state. The competition of small molecules for HSA binding in the presence of HSA Blue(TM) S1 results in low fluorescence intensities. This assay can be used as a high throughput screen tool to determine total binding to HSA at Site I.
Supplier: | AAT Bioquest |
Supplier-Nr: | 25400 |
Properties
Application: | HTS, binding assay |
Format: | Homog. |
Database Information
Handling & Safety
Storage: | -20°C |
Shipping: | +20°C (International: °C) |
Caution
Our products are for laboratory research use only: Not for administration to humans!
Our products are for laboratory research use only: Not for administration to humans!
Information about the product reference will follow.
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