추천 제품
Quality Level
SMILES string
[Na+].CCOc1ccc(Nc2ccc(cc2)C(\c3ccc(cc3)N(CC)Cc4cccc(c4)S([O-])(=O)=O)=C5\C=C/C(C=C5)=[N+](\CC)Cc6cccc(c6)S([O-])(=O)=O)cc1
InChI
1S/C45H45N3O7S2.Na/c1-4-47(31-33-9-7-11-43(29-33)56(49,50)51)40-23-15-36(16-24-40)45(35-13-19-38(20-14-35)46-39-21-27-42(28-22-39)55-6-3)37-17-25-41(26-18-37)48(5-2)32-34-10-8-12-44(30-34)57(52,53)54;/h7-30H,4-6,31-32H2,1-3H3,(H2,49,50,51,52,53,54);/q;+1/p-1
InChI key
NKLPQNGYXWVELD-UHFFFAOYSA-M
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애플리케이션
Detects most proteins at 50-100 ng per band
PhastGel® Blue R has been used for the staining of protein bands after SDS-PAGE (sodium dodecyl sulfate–polyacrylamide gel electrophoresis). It has also been used for the staining of cell clones in the culture media plates.
PhastGel® Blue R has been used for the staining of protein bands after SDS-PAGE (sodium dodecyl sulfate–polyacrylamide gel electrophoresis). It has also been used for the staining of cell clones in the culture media plates.
For detection of protein bands following electrophoresis.
재구성
One tablet makes 400 mL of a 0.1% staining solution.
법적 정보
PhastGel is a registered trademark of Cytiva
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
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In spite of the high sensitivity of silver staining and the wide dynamic range of various fluorescent detection methods, Coomassie Brilliant Blue staining is still the most widely used protein detection technique for proteins separated by polyacrylamide gel electrophoresis. There
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A modified Coomassie Brilliant Blue G 250 staining method for detecting chitinolytic enzymes in chitin-containing polyacrylamide gel electrophoresis (PAGE) is presented. The staining formed achromatic zones at the locations of the migrated enzyme. Using Streptomyces griseus chitinase, we have demonstrated
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