- Catalog number:
- E-BC-R327
- Applications:
- WB
- Size:
- 20mL
- Transportation temperature:
- 2~8°C
- Storage:
- -20°C
- Leadtime:
- 7~10 days
- Producer manual
Introduction
RIPA Lysis Buffer is a traditional rapid cell tissue lysate used as the preferred lysate for protein extraction from tissues or cells in the Western Blot assay.
Components
Cat | Product | 20 mL | 50 mL | 100 mL | Storage |
E-BC-R327 | RIPA Lysis(Strong) | 20 mL | 50 mL | 100 mL | -20°C |
E-BC-R287 | 100 mM PMSF | 200 μL | 500 μL | 1 mL | -20°C |
E-BC-R250 | 100 mM Na3VO4 | 200 μL | 500 μL | 1 mL | -20°C |
Manual | 1 copy | ||||
Instructions
1.For Tissue Samples
a. Take the samples, wash the tissue thoroughly with pre-cooled PBS (0.01M, pH7.4) to remove the surface blood and internal debris.
b. Weigh and smash the tissue, add an appropriate ratio of RIPA Lysis Buffer (add 10 μL PMSF and 10 μL Na3VO4 to 1 mL RIPA Lysis) and homogenizely lyse the tissue.
It is recommended to homogenize according to the ratio of tissue weight: RIPA volume = 3:10. For example,add 1mL RIPA Lysis Buffer to 0.3 g tissue sample, the specific volume can be adjusted according to experimental requirements.
c. Shake and lyse on the ice for 30 min after homogenization. And then sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lysis and reduce the viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4°C.
e. Take the supernatant and measure the protein concentration.
2.For Cell Sample
a. Collect the cells, wash them thoroughly with pre-cooled PBS (0.01 M, pH7.4) to remove the medium off (it is generally recommended to wash 3 times).
b. Add an appropriate ratio of RIPA Lysate Buffer (add 10 μL PMSF and 10 μL Na3VO4 to1 mL RIPA Lysis) and lyse on the ice for 30 min.
It is recommended to add 0.1 mL of RIPA Lysis Buffer to each well of a 6-well plates (the protein content in different cells may vary, and the volume of the RIPA Lysis Buffer added can be appropriately adjusted).
c. Sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lyse and reduce viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4°C.
e. Take the supernatant and measure the protein concentration.
RIPA Lysis Buffer components
50 mM Tris (pH7.4), 150 mM NaCl, 1% Triton X-100, 1% C24H39O4Na, 1 mM EDTA, 0.1% SDS, 10 mM NaF, 1 mM Na3VO4, 1 mM PMSF.
Storage
Store at -20°C for 12 months.
Cautions
1. For the protein extraction with RIPA Lysis Buffer, the whole process must be on the ice or at 4°C.
2. It is recommended to add 10 μL PMSF and 10 μL Na3VO4 to RAPI Lysis before use. If RIPA Lysis is crystalline state,dissolve at room temperature or in a warm water bath.
3. A cloud of transparent gels may appear in the RIPA Lysis product, which is a normal phenomenon because the lysis product is a compound containing genomic DNA. It is recommended to sonicate the sample for seconds. Take the supernatant after centrifugation for subsequent testing.
4.The protein sample lysed by RIPA cannot be measured by the Bradford method because of the high concentration of detergent in the lysis. It is recommended to measure the protein concentration by the BCA method.
5. For your safety and health, please wear the lab coat and disposable gloves before the experiments.
Introduction
RIPA Lysis Buffer is a traditional rapid cell tissue lysate used as the preferred lysate for protein extraction from tissues or cells in the Western Blot assay.
Components
Cat | Product | 20 mL | 50 mL | 100 mL | Storage |
E-BC-R327 | RIPA Lysis(Strong) | 20 mL | 50 mL | 100 mL | -20°C |
E-BC-R287 | 100 mM PMSF | 200 μL | 500 μL | 1 mL | -20°C |
E-BC-R250 | 100 mM Na3VO4 | 200 μL | 500 μL | 1 mL | -20°C |
Manual | 1 copy | ||||
Instructions
1.For Tissue Samples
a. Take the samples, wash the tissue thoroughly with pre-cooled PBS (0.01M, pH7.4) to remove the surface blood and internal debris.
b. Weigh and smash the tissue, add an appropriate ratio of RIPA Lysis Buffer (add 10 μL PMSF and 10 μL Na3VO4 to 1 mL RIPA Lysis) and homogenizely lyse the tissue.
It is recommended to homogenize according to the ratio of tissue weight: RIPA volume = 3:10. For example,add 1mL RIPA Lysis Buffer to 0.3 g tissue sample, the specific volume can be adjusted according to experimental requirements.
c. Shake and lyse on the ice for 30 min after homogenization. And then sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lysis and reduce the viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4°C.
e. Take the supernatant and measure the protein concentration.
2.For Cell Sample
a. Collect the cells, wash them thoroughly with pre-cooled PBS (0.01 M, pH7.4) to remove the medium off (it is generally recommended to wash 3 times).
b. Add an appropriate ratio of RIPA Lysate Buffer (add 10 μL PMSF and 10 μL Na3VO4 to1 mL RIPA Lysis) and lyse on the ice for 30 min.
It is recommended to add 0.1 mL of RIPA Lysis Buffer to each well of a 6-well plates (the protein content in different cells may vary, and the volume of the RIPA Lysis Buffer added can be appropriately adjusted).
c. Sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lyse and reduce viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4°C.
e. Take the supernatant and measure the protein concentration.
RIPA Lysis Buffer components
50 mM Tris (pH7.4), 150 mM NaCl, 1% Triton X-100, 1% C24H39O4Na, 1 mM EDTA, 0.1% SDS, 10 mM NaF, 1 mM Na3VO4, 1 mM PMSF.
Storage
Store at -20°C for 12 months.
Cautions
1. For the protein extraction with RIPA Lysis Buffer, the whole process must be on the ice or at 4°C.
2. It is recommended to add 10 μL PMSF and 10 μL Na3VO4 to RAPI Lysis before use. If RIPA Lysis is crystalline state,dissolve at room temperature or in a warm water bath.
3. A cloud of transparent gels may appear in the RIPA Lysis product, which is a normal phenomenon because the lysis product is a compound containing genomic DNA. It is recommended to sonicate the sample for seconds. Take the supernatant after centrifugation for subsequent testing.
4.The protein sample lysed by RIPA cannot be measured by the Bradford method because of the high concentration of detergent in the lysis. It is recommended to measure the protein concentration by the BCA method.
5. For your safety and health, please wear the lab coat and disposable gloves before the experiments.
Introduction
RIPA Lysis Buffer is a traditional rapid cell tissue lysate used as the preferred lysate for protein extraction from tissues or cells in the Western Blot assay.
Components
Cat | Product | 20 mL | 50 mL | 100 mL | Storage |
E-BC-R327 | RIPA Lysis(Strong) | 20 mL | 50 mL | 100 mL | -20°C |
E-BC-R287 | 100 mM PMSF | 200 μL | 500 μL | 1 mL | -20°C |
E-BC-R250 | 100 mM Na3VO4 | 200 μL | 500 μL | 1 mL | -20°C |
Manual | 1 copy | ||||
Instructions
1.For Tissue Samples
a. Take the samples, wash the tissue thoroughly with pre-cooled PBS (0.01M, pH7.4) to remove the surface blood and internal debris.
b. Weigh and smash the tissue, add an appropriate ratio of RIPA Lysis Buffer (add 10 μL PMSF and 10 μL Na3VO4 to 1 mL RIPA Lysis) and homogenizely lyse the tissue.
It is recommended to homogenize according to the ratio of tissue weight: RIPA volume = 3:10. For example,add 1mL RIPA Lysis Buffer to 0.3 g tissue sample, the specific volume can be adjusted according to experimental requirements.
c. Shake and lyse on the ice for 30 min after homogenization. And then sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lysis and reduce the viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4°C.
e. Take the supernatant and measure the protein concentration.
2.For Cell Sample
a. Collect the cells, wash them thoroughly with pre-cooled PBS (0.01 M, pH7.4) to remove the medium off (it is generally recommended to wash 3 times).
b. Add an appropriate ratio of RIPA Lysate Buffer (add 10 μL PMSF and 10 μL Na3VO4 to1 mL RIPA Lysis) and lyse on the ice for 30 min.
It is recommended to add 0.1 mL of RIPA Lysis Buffer to each well of a 6-well plates (the protein content in different cells may vary, and the volume of the RIPA Lysis Buffer added can be appropriately adjusted).
c. Sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lyse and reduce viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4°C.
e. Take the supernatant and measure the protein concentration.
RIPA Lysis Buffer components
50 mM Tris (pH7.4), 150 mM NaCl, 1% Triton X-100, 1% C24H39O4Na, 1 mM EDTA, 0.1% SDS, 10 mM NaF, 1 mM Na3VO4, 1 mM PMSF.
Storage
Store at -20°C for 12 months.
Cautions
1. For the protein extraction with RIPA Lysis Buffer, the whole process must be on the ice or at 4°C.
2. It is recommended to add 10 μL PMSF and 10 μL Na3VO4 to RAPI Lysis before use. If RIPA Lysis is crystalline state,dissolve at room temperature or in a warm water bath.
3. A cloud of transparent gels may appear in the RIPA Lysis product, which is a normal phenomenon because the lysis product is a compound containing genomic DNA. It is recommended to sonicate the sample for seconds. Take the supernatant after centrifugation for subsequent testing.
4.The protein sample lysed by RIPA cannot be measured by the Bradford method because of the high concentration of detergent in the lysis. It is recommended to measure the protein concentration by the BCA method.
5. For your safety and health, please wear the lab coat and disposable gloves before the experiments.
Introduction
RIPA Lysis Buffer is a traditional rapid cell tissue lysate used as the preferred lysate for protein extraction from tissues or cells in the Western Blot assay.
Components
Cat | Product | 20 mL | 50 mL | 100 mL | Storage |
E-BC-R327 | RIPA Lysis(Strong) | 20 mL | 50 mL | 100 mL | -20°C |
E-BC-R287 | 100 mM PMSF | 200 μL | 500 μL | 1 mL | -20°C |
E-BC-R250 | 100 mM Na3VO4 | 200 μL | 500 μL | 1 mL | -20°C |
Manual | 1 copy | ||||
Instructions
1.For Tissue Samples
a. Take the samples, wash the tissue thoroughly with pre-cooled PBS (0.01M, pH7.4) to remove the surface blood and internal debris.
b. Weigh and smash the tissue, add an appropriate ratio of RIPA Lysis Buffer (add 10 μL PMSF and 10 μL Na3VO4 to 1 mL RIPA Lysis) and homogenizely lyse the tissue.
It is recommended to homogenize according to the ratio of tissue weight: RIPA volume = 3:10. For example,add 1mL RIPA Lysis Buffer to 0.3 g tissue sample, the specific volume can be adjusted according to experimental requirements.
c. Shake and lyse on the ice for 30 min after homogenization. And then sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lysis and reduce the viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4°C.
e. Take the supernatant and measure the protein concentration.
2.For Cell Sample
a. Collect the cells, wash them thoroughly with pre-cooled PBS (0.01 M, pH7.4) to remove the medium off (it is generally recommended to wash 3 times).
b. Add an appropriate ratio of RIPA Lysate Buffer (add 10 μL PMSF and 10 μL Na3VO4 to1 mL RIPA Lysis) and lyse on the ice for 30 min.
It is recommended to add 0.1 mL of RIPA Lysis Buffer to each well of a 6-well plates (the protein content in different cells may vary, and the volume of the RIPA Lysis Buffer added can be appropriately adjusted).
c. Sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lyse and reduce viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4°C.
e. Take the supernatant and measure the protein concentration.
RIPA Lysis Buffer components
50 mM Tris (pH7.4), 150 mM NaCl, 1% Triton X-100, 1% C24H39O4Na, 1 mM EDTA, 0.1% SDS, 10 mM NaF, 1 mM Na3VO4, 1 mM PMSF.
Storage
Store at -20°C for 12 months.
Cautions
1. For the protein extraction with RIPA Lysis Buffer, the whole process must be on the ice or at 4°C.
2. It is recommended to add 10 μL PMSF and 10 μL Na3VO4 to RAPI Lysis before use. If RIPA Lysis is crystalline state,dissolve at room temperature or in a warm water bath.
3. A cloud of transparent gels may appear in the RIPA Lysis product, which is a normal phenomenon because the lysis product is a compound containing genomic DNA. It is recommended to sonicate the sample for seconds. Take the supernatant after centrifugation for subsequent testing.
4.The protein sample lysed by RIPA cannot be measured by the Bradford method because of the high concentration of detergent in the lysis. It is recommended to measure the protein concentration by the BCA method.
5. For your safety and health, please wear the lab coat and disposable gloves before the experiments.
