Product Name :
Nuclear and Cytoplasmic Extraction Kit Applications :
Nuclear and Cytoplasmic Extraction Background :
For research of cell protein, the separation of cytosol and nucleus protein attracted researchers’ attention. This requires effective reagents to separate cytoplasmic and nuclear extracts from cultured mammalian cells. The kit enables stepwise proteins: Reagent A disrupts cell membrane while not acts on nuclear. Reagent B lyses the nuclei. It is effective to separate cytoplasmic and nuclear proteins in short time with this kit. The extracts are suitable for WB, co-IP and purification of proteins. Due to the reagents in this kit, BCA Protein Assay method is recommended to quantify the protein concentrations of extracts. There are no protease inhibitors in this kit, prepare protease inhibitors before use. Alternative Name :
1) This kit is only used for mammalian cell. 2) Avoid freeze-thaw cycles. Recommend to aliquot before stored at -20℃ or -80℃.Period of validity is 12 months(-20℃); 3) This kit doesn’t contain protease inhibitors, prepare protease inhibitor before use. 4) Resuspend the precipitate with reagent B in the tube as you can as possible, but there might be flocculent fragments. That causes no impact on the nuclear extract. 5) All steps on ice. Classification :
WB Related Reagents Format :
Liquid Contents :
1) Reagent A: 50ml, stored at -20℃, recommend to aliquot before stored at -20℃. 2) Reagent B: 10ml, stored at -20℃, recommend to aliquot before stored at -20℃. Storage & Shelf Life :
A: stored at -20℃, recommend to aliquot before stored at -20℃. B: stored at -20℃, recommend to aliquot before stored at -20℃. Procedure :
1) For adherent mammalian cells(1-10*106 cells): the cells were harvested with trypsin-EDTA, the centrifuged at 500g for 3min, 4℃; For suspension mammalian cells(1-10*106 cells): the cells were centrifuged at 500g for 3min. Resuspend and wash the cells with PBS in a 1.5 ml tube. Then centrifuge the cells at 500g for 3min, remove and discard the supernatant as much as possible. 2) Add 800-1000µl reagent A (for 1-10*106 cells) with protease inhibitors to the precipitate; Resuspend the precipitate and vortex the tube for 15s. 3) Place the tube on ice for 20min. During this period, vortex the tube for 15s to resuspend the precipitate each 5min. 4) Centrifuge the tube at 3000g for 10min, 4℃. Transfer the supernatant (cytoplasmic extracts) to a new tube. Store at 4℃ (for short term) or -80℃ (for long term). 5) Add 500µl reagent A with protease inhibitors to the precipitate (left in the tube during step 4), resuspend and wash the precipitate. Centrifuge at 3000g for 10min. Remove and discard the supernatant. (May be omitted if you can almost transfer the cytoplasmic extracts completely in step 4.) 6) Add 150-200µl reagent B with protease inhibitors to the precipitate (left in the tube during step 4 or 5). Resuspend the precipitate and vortex the tube for 15s. Place the tube on ice for 10min. Then vortex the tube for 15s to resuspend the precipitate every 5min, for total 20min. 7) Centrifuge the tube at 12000g for 20min, 4℃. Transfer the supernatant (nuclear extract) to a new tube. Store at 4℃ (for short term) or -80℃ (for long term). Research use :
For research use only, not for use in diagnostic procedures. Expiration Date :
Period of validity is 12 months.
Nuclear and Cytoplasmic Extraction Kit Applications :
Nuclear and Cytoplasmic Extraction Background :
For research of cell protein, the separation of cytosol and nucleus protein attracted researchers’ attention. This requires effective reagents to separate cytoplasmic and nuclear extracts from cultured mammalian cells. The kit enables stepwise proteins: Reagent A disrupts cell membrane while not acts on nuclear. Reagent B lyses the nuclei. It is effective to separate cytoplasmic and nuclear proteins in short time with this kit. The extracts are suitable for WB, co-IP and purification of proteins. Due to the reagents in this kit, BCA Protein Assay method is recommended to quantify the protein concentrations of extracts. There are no protease inhibitors in this kit, prepare protease inhibitors before use. Alternative Name :
1) This kit is only used for mammalian cell. 2) Avoid freeze-thaw cycles. Recommend to aliquot before stored at -20℃ or -80℃.Period of validity is 12 months(-20℃); 3) This kit doesn’t contain protease inhibitors, prepare protease inhibitor before use. 4) Resuspend the precipitate with reagent B in the tube as you can as possible, but there might be flocculent fragments. That causes no impact on the nuclear extract. 5) All steps on ice. Classification :
WB Related Reagents Format :
Liquid Contents :
1) Reagent A: 50ml, stored at -20℃, recommend to aliquot before stored at -20℃. 2) Reagent B: 10ml, stored at -20℃, recommend to aliquot before stored at -20℃. Storage & Shelf Life :
A: stored at -20℃, recommend to aliquot before stored at -20℃. B: stored at -20℃, recommend to aliquot before stored at -20℃. Procedure :
1) For adherent mammalian cells(1-10*106 cells): the cells were harvested with trypsin-EDTA, the centrifuged at 500g for 3min, 4℃; For suspension mammalian cells(1-10*106 cells): the cells were centrifuged at 500g for 3min. Resuspend and wash the cells with PBS in a 1.5 ml tube. Then centrifuge the cells at 500g for 3min, remove and discard the supernatant as much as possible. 2) Add 800-1000µl reagent A (for 1-10*106 cells) with protease inhibitors to the precipitate; Resuspend the precipitate and vortex the tube for 15s. 3) Place the tube on ice for 20min. During this period, vortex the tube for 15s to resuspend the precipitate each 5min. 4) Centrifuge the tube at 3000g for 10min, 4℃. Transfer the supernatant (cytoplasmic extracts) to a new tube. Store at 4℃ (for short term) or -80℃ (for long term). 5) Add 500µl reagent A with protease inhibitors to the precipitate (left in the tube during step 4), resuspend and wash the precipitate. Centrifuge at 3000g for 10min. Remove and discard the supernatant. (May be omitted if you can almost transfer the cytoplasmic extracts completely in step 4.) 6) Add 150-200µl reagent B with protease inhibitors to the precipitate (left in the tube during step 4 or 5). Resuspend the precipitate and vortex the tube for 15s. Place the tube on ice for 10min. Then vortex the tube for 15s to resuspend the precipitate every 5min, for total 20min. 7) Centrifuge the tube at 12000g for 20min, 4℃. Transfer the supernatant (nuclear extract) to a new tube. Store at 4℃ (for short term) or -80℃ (for long term). Research use :
For research use only, not for use in diagnostic procedures. Expiration Date :
Period of validity is 12 months.
Parthenolide reverses doxorubicin resistance in human lungcarcinoma A549 cells by attenuating NF- B activation and HSP70 up-regulation
PMCID: Pubmed No.:23792430
Tetrandrine Suppresses Lipopolysaccharide-Induced Microglial Activation by Inhibiting NF-κB and ERK Signaling Pathways in BV2 Cells
PMCID: Pubmed No.:25115855
Tetramethylpyrazine prevents ethanol-induced hepatocyte injury via activation of nuclear factor erythroid 2-related factor 2
PMCID: Pubmed No.:26341692
Quercetin phospholipid complex significantly protects against oxidative injury in ARPE-19 cells associated with activation of Nrf2 pathway
PMCID: Pubmed No.:26643168
Anti-osteoclastogenic activity of isoliquiritigenin via inhibition of NF-κB-dependent autophagic pathway
PMCID: Pubmed No.:26947453
Tetrandrine Suppresses Lipopolysaccharide-Induced Microglial Activation by Inhibiting NF-κB and ERK Signaling Pathways in BV2 Cells
PMCID: Pubmed No.:25115855
Quercetin phospholipid complex significantly protects against oxidative injury in ARPE-19 cells associated with activation of Nrf2 pathway
PMCID: Pubmed No.:26643168
Anti-osteoclastogenic activity of isoliquiritigenin via inhibition of NF-κB-dependent autophagic pathway
PMCID: Pubmed No.:26947453
Blocking peptide available as BD0030P