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Analysis of Glucose-binding proteins (GBPs) by Differential Scanning Fluorimetry(DSF) (CAT#: STEM-MB-0828-WXH)

Introduction

Glucose-binding proteins (GBPs) belong to a large family of soluble periplasmic proteins that support distinct biological functions in Gram-negative bacteria. In bacteria, this periplasmic component is the primary determinant of the specificity of the transport complex as a whole.




Principle

Differential Scanning Fluorimetry measures protein thermal unfolding by monitoring changes in fluorescence emission of a sample upon heating. This allows the determination of protein thermostability and complex formation even with weakly binding ligands by thermal shift assay. Differential Scanning Fluorimetry is therefore ideally suited for screening of optimum buffer conditions like pH, buffer composition and ionic strength. The technique is applicable to any biological sample, from soluble proteins to integral membrane proteins.

Applications

To identify low-molecular-weight ligands that bind and stabilize purified proteins.
To measure the denaturation and unfolding of proteins.

Procedure

1. Preparation of compound solutions
2. Preparation of buffer/additive screen plates
3. Preparation of compound storage plates
4. Equipment preparation
5. Sample preparation
82. Performing the scan

Materials

Real-time PCR instrument
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