Electrophoresis Gel Stains
Bioworld Rapid Coomassie Stain, 100 mL
Item# 21470008This stain is fast and sensitive in staining proteins in acrylimide gels. Its features include: a) completion within 30-60 minutes, b) unnecessary destaining, c) being highly sensitive, it detects as little as 30 ng of protein, d) yields sharper bands than those stained with conventional Coomassie Blue, and e) gels can be restained with Silver. Solution provided as 2x concentrate.
Bioworld Express Coomassie Stain, R-250, 100 mL
Express Coomassie Stain detects as little as 15 ng of protein and gives complete band detection within 50 minutes. Its ideal for densitometry, and its able to be restained with silver. This stain can be used more than once. Express Coomassie is a colloidal suspension of Coomassie blue that preferentially binds to protein and eliminates the unwanted destaining step.Appearance: LiquidHS Code : 32041200Melting Point: 100 °C
Sigma Aldrich Fine Chemicals Biosciences Brilliant Blue R | 6104-59-2 | MFCD00041762 | 100g
Brilliant Blue R | Mol Wt: 825.97 | 6104-59-2 | MFCD00041762 | 100g
Sigma Aldrich Fine Chemicals Biosciences Brilliant Blue R Dye content ~50 %, Technical grade | 6104-59-2 | MFCD00041762 | 5G
Brilliant Blue R Dye content ~50 %, Technical grade | Mol Wt: 825.97 | 6104-59-2 | MFCD00041762 | 5G
Alkali Scientific SmartGlow™ Safe Green Pre Nucleic Acid Stain, Loading Dye, Trial Size
SmartGlow Nucleic Acid Stain is ideal for excitation of nucleic acids with UV or visible blue light transilluminators. Unlike EtBR, SmartGlow it is non-mutagenic and does not require special methods of disposal. SmartGlow PS (Pre Stain) can be used as a direct replacement for Ethidium Bromide in agarose and polyacrylamide gel electrophoresis. The stain emits green fluorescence when bound to dsDNA, ssDNA and RNA. SmartGlow PS exhibits excitation peaks at 290nm and 490nm, allowing it to be used with UV and blue light. SmartGlow LD (Loading Dye) is supplied at 6X concentration and is added directly to the samples. No dye needs to be added to the gel or running buffer. After electrophoretic separation, view and document your results using a UV or blue light illuminator. SmartGlow LD emits green fluorescence when bound to dsDNA, ssDNA and RNA. Replaces hazardous EtBr Excitation by UV or blue light Non-mutagenic, environmentally safe Two types: PS (Pre-Stain) LD (Loading Dye)
Bioworld Coomassie Blue R-250 (2X), 500 mL
Stain for location and detection of proteins. Protocol: After SDS-PAGE, transfer the gels in fixing solution (30% methanol and 7% acetic acid) for 30 min. under constant agitation. Replace the fixing solution, submerge the gel in stain and shake the gel gently gor 2-4 hrs. Pour off the stain, rinse the gel briefly with fixing solution and cover the gel with fresh fixing solution for 30 min. Repeat and continue destaining until distinct blue bands against a clear background are obtained. Store the gel in 7% acetic acid solution. Photograph or dry the gel according to your standard protocol.Synonym: Brilliant blue R; Coomassie brilliant blue R-250; Acid Blue 83; CI 42660Appearance: Liquid
Bioworld Coomassie Blue G-250 (2X), 500 mL
A commonly used analytical biochemistry dye and P2X7 antagonistStain for location and detection of proteins. Protocol: After SDS-PAGE, transfer the gels in fixing solution (30% methanol and 7% acetic acid) for 30 min. under constant agitation. Replace the fixing solution, submerge the gel in stain and shake the gel gently gor 2-4 hrs. Pour off the stain, rinse the gel briefly with fixing solution and cover the gel with fresh fixing solution for 30 min. Repeat and continue destaining until distinct blue bands against a clear background are obtained. Store the gel in 7% acetic acid solution. Photograph or dry the gel according to your standard protocol.Synonym: Synonym: Acid blue 90, Coomassie Brilliant Blue GAppearance: LiquidHS Code : 32041200
Bioworld Coomassie Blue G-250 (2X), 1 L
A commonly used analytical biochemistry dye and P2X7 antagonistStain for location and detection of proteins. Protocol: After SDS-PAGE, transfer the gels in fixing solution (30% methanol and 7% acetic acid) for 30 min. under constant agitation. Replace the fixing solution, submerge the gel in stain and shake the gel gently gor 2-4 hrs. Pour off the stain, rinse the gel briefly with fixing solution and cover the gel with fresh fixing solution for 30 min. Repeat and continue destaining until distinct blue bands against a clear background are obtained. Store the gel in 7% acetic acid solution. Photograph or dry the gel according to your standard protocol.Synonym: Synonym: Acid blue 90, Coomassie Brilliant Blue GAppearance: LiquidHS Code : 32041200
Revvity Health Sciences Inc IVISense Cat B 750 FAST Fluorescent Probe
IVISense Cat B 750 FAST Fluorescent Probe
Gold Biotechnology Inc GelRedTM Nucl Acid Gel Stain
GelRed is an ultra-sensitive extremely stable and environmentally safe fluorescent nucleic acid dye designed to replace the highly toxic ethidium bromide (EtBr) for staining dsDNA ssDNA or RNA in agarose gels or polyacrylamide gels GelRed is far more sensitive than EtBr without requiring a destaining step GelRed and EtBr have virtually the same spectra so you can directly replace EtBr with GelRed without changing your existing imaging system