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Experience these additional benefits:
- Wide dynamic range, over 3-orders of magnitude - reduce dilution requirements prior to assay
- Low protein-protein variability - improve confidence of accuracy for complex samples
- No time-consuming heating and protein reduction steps - eliminates additional steps and speeds processing
- Assay tolerates interfering compounds (DNA and solubilizing reagents) - eliminates
additional steps, such as precipitation to remove buffers or detergents that may alter protein content
- Stable for up to 6 hours - allows freedom to perform additional work concurrently
- No strong solvents and acids - improves safe handling
- No special instrument requirements - Designed for use in a wide range of fluorescence measuring instruments
Order Information
| Product Code |
Product Name |
Size |
| FP0010 |
FluoroProfile Protein Quantification Kit |
1 KT |
Figure 1: Excitation and Fluorescence Emission
Spectra
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Figure 2: Typical Standard Curve
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Figure 3: Fluorescence Signal Variation with Different Proteins
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Interfering Compounds
| Compound |
Concentration |
CHAPS |
|
0.05% |
|
| |
SDS |
|
0.1% |
|
| |
Thiourea |
|
500 mM |
|
| |
EDTA |
|
20 mM |
|
| |
NaCl |
|
100 mM |
|
| |
TBP |
|
10 mM |
|
| |
Urea |
|
1 M |
|
| |
TCEP |
|
2 mM |
|
| |
Glycerol |
|
25% |
|
| |
Iodoacetamide |
|
20 mM |
|
| |
2-Mercaptoethanol |
|
20 mM |
|
| |
Sucrose |
|
250 mM |
|
| |
Tris |
|
500 µM |
|
| |
TRITON X-100 |
|
0.002 % |
|
| |
TWEEN® |
|
0.005 % |
|
| |
Note: This is not a complete list of incompatible compounds. One may assay the protein of interest in ultrapure water alone, then in sample buffer with possible interfering substances. Comparison of the readings will indicate if interference exists. Alternatively, the interfering substance may be removed using dialysis or protein precipitation using the ProteoPrep® Protein Precipitation Kit (PROT-PR).
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