NS1226
Cysteine Sulfenic Acid Probe (DCP-Bio1)
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221,00 €
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About This Item
221,00 €
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Descripción general
The most commonly used method for assessing whether proteins are modified to contain cysteine sulfenic acid employs derivitization with 5,5-dimethyl-1,3-cyclohexanedione (dimedone), and subsequent detection with an antibody against dimedone-modified proteins. However, new reagents have been developed to simplify the analysis and isolation of proteins bearing cysteine sulfenic acid. DCP-Bio1, which consists of the sulfenic acid-reactive 3-(2,4-dioxocyclohexyl) propyl (DCP) appended to biotin, is a useful reagent for characterizing cellular cysteine sulfenic acid.
Aplicación
Solutions:
DCP-Bio1 stock solution
Resuspend entire contents of vial in 10 µL DMSO for a final concentration of 250 mM
Stock lysis buffer
50 mM Tris-HCl, pH 7.5
100 mM Sodium Chloride
0.1% SDS
0.5% Sodium Deoxycholate
0.5% NP-40
0.5% Triton X-100
Working lysis buffer
On the day of the assay, supplement stock lysis buffer with:
50 mM Sodium Fluoride
1 mM PMSF
1 mM DCP-Bio1
100 µM DTPA (Diethylene triamine pentaacetic acid)
10 mM N-ethylmaleimide
10 mM iodoacetamide
200 U/mL catalase
1x protease inhibitor cocktail
Cell treatment and lysis:
1)Seed adherent cells in 100 mm cell culture dishes, or other plate as desired.
2)Change to fresh growth media 30 minutes before selected treatments.
3)Wash all plates 2 times with 10 mL 1x PBS.
4)Add 150 µL working lysis buffer to plates and scrape cells.
5)Incubate lysates on ice for 1-2 hours.
6)Centrifuge lysates at 10,000 rpm for 10 minutes and collect supernatant.
7)Remove un-reacted DCP-Bio1 and other small molecules using Bio-Rad P6-Spin Columns (PN: 732-6227) following manufacturer′s instructions.
8)Measure protein concentration.
9)Perform biochemical analysis of interest.
DCP-Bio1 stock solution
Resuspend entire contents of vial in 10 µL DMSO for a final concentration of 250 mM
Stock lysis buffer
50 mM Tris-HCl, pH 7.5
100 mM Sodium Chloride
0.1% SDS
0.5% Sodium Deoxycholate
0.5% NP-40
0.5% Triton X-100
Working lysis buffer
On the day of the assay, supplement stock lysis buffer with:
50 mM Sodium Fluoride
1 mM PMSF
1 mM DCP-Bio1
100 µM DTPA (Diethylene triamine pentaacetic acid)
10 mM N-ethylmaleimide
10 mM iodoacetamide
200 U/mL catalase
1x protease inhibitor cocktail
Cell treatment and lysis:
1)Seed adherent cells in 100 mm cell culture dishes, or other plate as desired.
2)Change to fresh growth media 30 minutes before selected treatments.
3)Wash all plates 2 times with 10 mL 1x PBS.
4)Add 150 µL working lysis buffer to plates and scrape cells.
5)Incubate lysates on ice for 1-2 hours.
6)Centrifuge lysates at 10,000 rpm for 10 minutes and collect supernatant.
7)Remove un-reacted DCP-Bio1 and other small molecules using Bio-Rad P6-Spin Columns (PN: 732-6227) following manufacturer′s instructions.
8)Measure protein concentration.
9)Perform biochemical analysis of interest.
Componentes
Calidad
Almacenamiento y estabilidad
Cláusula de descargo de responsabilidad
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Certificados de análisis (COA)
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