S5692
SYPRO® Orange Protein Gel Stain
Sinónimos:
SYPRO® dye, protein gel stain
About This Item
Productos recomendados
shelf life
≥6 mo. (when stored desiccated and protected from light at room temperature, 4 °C or 20 °C.)
technique(s)
protein staining: suitable
fluorescence
λex 300,470 nm; λem 570 nm
General description
SYPRO Orange is:
- Highly sensitive. The stain can detect 1 to 2 ng of protein per minigel band, making it more sensitive than Coomassie Brilliant Blue or silver staining.
- Rapid. Staining is complete in less than one hour
- Simple. After electrophoresis, the gel is stained, rinsed and photographed; no fixation or destaining steps are required
- Compatible with standard laboratory equipment. Stained proteins can be visualized with a standard 300 nm UV transilluminator or laser scanner.
- Cost-effective. Staining with SYPRO Orange is less expensive than silver staining and requires less time.
- Low protein-to-protein variability. The dye interacts with the SDS coat around the protein, giving more consistent staining between different types of proteins compared to Coomassie or silver staining.
- Selective for proteins. SYPRO Orange detects proteins as small as 6.5 kDa and does not stain nucleic acids or lipopolysaccharides. It does stain glycosylated proteins.
- Broad linear range of detection. The fluorescence intensity of the stained bands is linear with protein quantity over three orders of magnitude (a much broader range than either Coomassie or silver staining).
Application
Caution
Legal Information
related product
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
188.6 °F - closed cup
flash_point_c
87 °C - closed cup
Certificados de análisis (COA)
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Artículos
Sigma offers EZBlue™ and ProteoSilver™ reagents for protein visualization, suitable for proteomics and traditional PAGE formats.
Identify causes and remedies for SDS-PAGE sample preparation challenges and optimize electrophoresis conditions.
Protocolos
Protocol for sample preparation for cell lysis and efficient protein extraction from cultured tissues and cells for subsequent Western blotting.
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