Search
Citations & References (8)
Invitrogen™
Coomassie Fluor™ Orange Protein Gel Stain (Ready-To-Use Solution)
Molecular Probes' proprietary Coomassie Fluor Orange protein gel stain provides fast, simple, sensitive staining of proteins separated by SDS-PAGE. AfterRead more
| Catalog Number | Quantity |
|---|---|
| C33250 | 1 L |
Catalog number C33250
Price (BRL)
1.198,77
Each
Quantity:
1 L
Price (BRL)
1.198,77
Each
Molecular Probes' proprietary Coomassie Fluor Orange protein gel stain provides fast, simple, sensitive staining of proteins separated by SDS-PAGE. After electrophoresis, the gel is stained, rinsed and photographed. Staining is complete in less than an hour – no separate fixation or destaining steps are required, and there is no risk of overstaining the gel. Stained proteins can be visualized using a standard 300 nm UV transilluminator or a laser-based scanner. Coomassie Fluor Orange protein gel stain is also available in a 5 liter size (Cat. no. C-33251).
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection LocationIn-Gel Detection
Detection MethodFluorescence
Excitation/Emission300, 470/570 nm
Product LineCoomassie Fluor
Product TypeProtein Gel Stain
Quantity1 L
Shipping ConditionRoom Temperature
Target MoleculeProtein
Label or DyeCoomassie Fluor Orange
Unit SizeEach
Contents & Storage
Store at room temperature and protect from light.
Citations & References (8)
Citations & References
Abstract
Molecular mechanism of the inhibitory effect of cobalt ion on thermolysin activity and the suppressive effect of calcium ion on the cobalt ion-dependent inactivation of thermolysin.
Journal:J Biochem
PubMed ID:17405797
'Thermolysin activity in the hydrolysis of N-[3-(2-furyl)acryloyl]-glycyl-l-leucine amide (FAGLA) and FA-l-leucyl-l-alanine amide (FALAA) was examined at various Co(2+) and Ca(2+) concentrations. It decreased to 28% with increasing [Co(2+)] up to 18 mM. The Co(2+)-dependent inactivation was in part suppressed by adding Ca(2+) ion up to 0.5 mM, but 33% of
Covalently dimerized SecA is functional in protein translocation.
Journal:J Biol Chem
PubMed ID:16115882
'The ATPase SecA provides the driving force for the transport of secretory proteins across the cytoplasmic membrane of Escherichia coli. SecA exists as a dimer in solution, but the exact oligomeric state of SecA during membrane binding and preprotein translocation is a topic of debate. To study the requirements of
Recombinant human immunodeficiency virus type 1 integrase exhibits a capacity for full-site integration in vitro that is comparable to that of purified preintegration complexes from virus-infected cells.
Journal:J Virol
PubMed ID:15956566
Retrovirus preintegration complexes (PIC) in virus-infected cells contain the linear viral DNA genome (approximately 10 kbp), viral proteins including integrase (IN), and cellular proteins. After transport of the PIC into the nucleus, IN catalyzes the concerted insertion of the two viral DNA ends into the host chromosome. This successful insertion
Genetic determinants of Silicibacter sp. TM1040 motility.
Journal:J Bacteriol
PubMed ID:19482930
Silicibacter sp. TM1040 is a member of the marine Roseobacter clade of Alphaproteobacteria that forms symbioses with unicellular eukaryotic phytoplankton, such as dinoflagellates. The symbiosis is complex and involves a series of steps that physiologically change highly motile bacteria into cells that readily form biofilms on the surface of the
Role for leptin in promoting glucose mobilization during acute hyperosmotic stress in teleost fishes.
Journal:
PubMed ID:24194509
Osmoregulation is critical for survival in all vertebrates, yet the endocrine regulation of this metabolically expensive process is not fully understood. Specifically, the function of leptin in the regulation of energy expenditure in fishes, and among ectotherms, in general, remains unresolved. In this study, we examined the effects of acute