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TLR2/NF-kB/SEAP Stable Reporter Cell Line、TLR2/NF-kB/SEAP 穩(wěn)轉(zhuǎn)報(bào)告細(xì)胞株
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產(chǎn)品簡介
產(chǎn)品介紹
Description（產(chǎn)品描述）
The TLR2 reporter cell line is a stably co-transfected cell line which expresses full-length human Toll-like receptor 2 （TLR2） and the secreted alkaline phosphatase （SEAP） reporter gene under the transcriptional control of an NF-kB response element. The TLR2 reporter cell line has been validated by flow cytometry （Fig. 1） and ligand dose response assay （Fig. 2 and Fig. 3）.
IMGENEX is pleased to offer the TLR2 NFkB Reporter Assay as a service.
Complete Growth Medium（*培養(yǎng)基）
DMEM with 4.5 g/L glucose + 10% FBS + 4 mM L-glutamine + 1 mM sodium pyruvate + 100 units/ml penicillin + 100 ug/ml streptomycin + 10 ug/ml blasticidin + 500 ug/ml G418 （Geneticin）
Note: The selection agents are blasticidin and G418.
Note: The selection agents are blasticidin and G418.
Application（應(yīng)用）
The TLR2 reporter line can be used for TLR2-dependent functional assays as well as screening of TLR2 agonists or antagonists
Product Handling Protocol（產(chǎn)品處理協(xié)議）
Note: Please read the entire data sheet before thawing. It is recommended that users follow good tissue culture practice. The TLR2 reporter line is sterile and all work should be performed under sterile conditions.
1. Prepare a sterile 15-ml tube with 9 ml fresh medium without selection agents pre-warmed at 37oC.
2. Thaw the TLR2 reporter cell line vial quickly in a 37oC water bath, keeping the cap portion out of the water to avoid any possible contamination.
3. Upon thawing, take the vial out of the water and clean it with 70% ethanol to decontaminate.
4. Transfer contents to the 15-ml tube （Step 1） and mix with medium by gentle inversion of tube.
5. Centrifuge at 1,000 RPM for 5 minutes.
6. Remove supernatant and resuspend pellet in 10 ml of fresh medium without selection agents.
Note: It is important to grow the reporter cells at this stage without any selection agents.
7. Transfer the TLR2 reporter cell line into a 25-cm2 tissue culture flask and incubate at 37oC in a 95% air-5% CO2 mixture.
8. After cells settle down （in 1-3 days）, remove the medium and replace with fresh complete growth medium containing selection agents.
9. At 70-80% confluency, detach the cells by trypsinization and split into new flasks with fresh complete growth medium.
10. Freeze the TLR2 reporter cell line at 3~4 x 10^6 cells/ml per cryogenic vial. For optimal viability after freezing, freeze cells when they have reached log phase growth （95-98% confluency）. Detach by trypsinization at 37oC for 5 min, and harvest by mixing with 3 volumes of fresh medium followed by centrifugation （Step 5）. Resuspend the pellet in freeze media （FBS with 10% DMSO）. Add suspension to cryogenic vials in 1 ml aliquots. Place cryogenic vials, in a tissue culture approved cryogenic vial container, in -80oC freezer for 24-48 hours. After 24-48 hours, move the vials into liquid nitrogen storage.
1. Prepare a sterile 15-ml tube with 9 ml fresh medium without selection agents pre-warmed at 37oC.
2. Thaw the TLR2 reporter cell line vial quickly in a 37oC water bath, keeping the cap portion out of the water to avoid any possible contamination.
3. Upon thawing, take the vial out of the water and clean it with 70% ethanol to decontaminate.
4. Transfer contents to the 15-ml tube （Step 1） and mix with medium by gentle inversion of tube.
5. Centrifuge at 1,000 RPM for 5 minutes.
6. Remove supernatant and resuspend pellet in 10 ml of fresh medium without selection agents.
Note: It is important to grow the reporter cells at this stage without any selection agents.
7. Transfer the TLR2 reporter cell line into a 25-cm2 tissue culture flask and incubate at 37oC in a 95% air-5% CO2 mixture.
8. After cells settle down （in 1-3 days）, remove the medium and replace with fresh complete growth medium containing selection agents.
9. At 70-80% confluency, detach the cells by trypsinization and split into new flasks with fresh complete growth medium.
10. Freeze the TLR2 reporter cell line at 3~4 x 10^6 cells/ml per cryogenic vial. For optimal viability after freezing, freeze cells when they have reached log phase growth （95-98% confluency）. Detach by trypsinization at 37oC for 5 min, and harvest by mixing with 3 volumes of fresh medium followed by centrifugation （Step 5）. Resuspend the pellet in freeze media （FBS with 10% DMSO）. Add suspension to cryogenic vials in 1 ml aliquots. Place cryogenic vials, in a tissue culture approved cryogenic vial container, in -80oC freezer for 24-48 hours. After 24-48 hours, move the vials into liquid nitrogen storage.
Safety Considerations（安全注意事項(xiàng)）
Assume all cultures are hazardous since they may harbor latent viruses or other organisms that are uncharacterized. The following safety precautions should be observed.
• Use pipette aids to prevent ingestion and keep aerosols down to a minimum.
• No eating, drinking or smoking while handling the reporter cell line.
• Wash hands after handling the reporter cell line and before leaving the lab.
• Decontaminate work surface with disinfectant or 70% ethanol before and after working with cells.
• All waste should be considered hazardous.
• Dispose of all liquid waste after each experiment and treat with bleach.
• Use pipette aids to prevent ingestion and keep aerosols down to a minimum.
• No eating, drinking or smoking while handling the reporter cell line.
• Wash hands after handling the reporter cell line and before leaving the lab.
• Decontaminate work surface with disinfectant or 70% ethanol before and after working with cells.
• All waste should be considered hazardous.
• Dispose of all liquid waste after each experiment and treat with bleach.
Figure 1. Flow cytometric analysis. Cell surface expression of TLR2 on the TLR2 reporter line was analyzed by flow cytometry using a PE-conjugated TLR2 antibody （IMG-416D）. Flow samples were prepared using the Cell Surface TLR Staining Flow Kit （10099K）. Purple: Cells alone; Green: NF-kB/ SEAPorter™ HEK 293 cell line （IML-101） stained with anti-TLR2-PE （IMG-416D）; Red: TLR2 reporter cell line stained with anti-TLR2-PE （IMG-416D）.
Figure 2. Evaluation of the functional activity of the TLR2/NF-kB SEAPorterTM HEK 293 cell line by ligand dose response assay. TLR2/NF-kB SEAPorterTM HEK 293 cells （IML-102） were plated in 96-well plates at 5 x 10^4 cells/well. After 16 h, cells were stimulated with various amount of Pam3CSK4 （IMG-2201） for 24 h. SEAP was analyzed using the SEAPorter Assay Kit （10055K）. A. Pam3CSK4-mediated TLR2 activation, as measured by SEAP activity, was increased in a dose dependent manner. B. The values from （A） were used to determine the EC50 of Pam3CSK4. The EC50, or the half maximal activity concentration, represents the concentration of Pam3CSK4 that was required for 50% activation of TLR2 as measured by SEAP activity.
Data Summary: Pam3CSK4 activated the IML-102 cell line in a dose response manner, of which EC50 was measured as 0.387 ng/ml.
Data Summary: Pam3CSK4 activated the IML-102 cell line in a dose response manner, of which EC50 was measured as 0.387 ng/ml.
Figure 3. Evaluation of the functional activity of the TLR2/NF-kB SEAPorterTM HEK 293 cell line by ligand dose response assay. TLR2/NF-kB SEAPorterTM HEK 293 cells （IML-102） were plated in 96-well plates at 5 x 10^4 cells/well. After 16 h, cells were stimulated with various amount of MALP-2 （IMG-2206） for 24 h. SEAP was analyzed using the SEAPorter Assay Kit （10055K）. A. MALP2-mediated TLR2 activation, as measured by SEAP activity, was increased in a dose dependent manner. B. The values from （A） were used to determine the EC50 of MALP-2. The EC50, or the half maximal activity concentration, represents the concentration of MALP-2 that was required for 50% activation of TLR2 as measured by SEAP activity.
Data Summary: MALP-2 activated the IML-102 cell line in a dose response manner, of which EC50 was measured as 0.075 ng/ml.
Data Summary: MALP-2 activated the IML-102 cell line in a dose response manner, of which EC50 was measured as 0.075 ng/ml.
Reference（參考文獻(xiàn)）
1. Jaklien C. Leemans, Geurt Stokman, Nike Claessen, Kasper M. Rouschop, Gwendoline J.D. Teske, Carsten J. Kirschning, Shizuo Akira, Tom van der Poll, Jan J. Weening, Sandrine Florquin. Renal-associated TLR2 mediates ischemia/reperfusion injury in the kidney. J Clin Invest. 2005 October 1; 115（10）: 2894–2903.
2. Monika Madan, Salomon Amar. Toll-Like Receptor-2 Mediates Diet and/or Pathogen Associated Atherosclerosis: Proteomic Findings. PLoS ONE. 2008; 3（9）: e3204.
3. Carsten J Kirschning, Stefan Dreher, Björn Maaß, Sylvia Fichte, Jutta Schade, Mario Köster, Andreas Noack, Werner Lindenmaier, Hermann Wagner, Thomas Böldicke. Generation of anti-TLR2 intrabody mediating inhibition of macrophage surface TLR2 expression and TLR2-driven cell activation. BMC Biotechnol. 2010; 10: 31.
4. Roger P.M. Sutmuller, Martijn H.M.G.M. den Brok, Matthijs Kramer, Erik J. Bennink, Liza W.J. Toonen, Bart-Jan Kullberg, Leo A. Joosten, Shizuo Akira, Mihai G. Netea, Gosse J. Adema. Toll-like receptor 2 controls expansion and function of regulatory T cells. J Clin Invest. 2006 February 1; 116（2）: 485–494.
5. Jaklien C. Leemans, Loes M. Butter, Wilco P. C. Pulskens, Gwendoline J. D. Teske, Nike Claessen, Tom van der Poll, Sandrine Florquin. The Role of Toll-Like Receptor 2 in Inflammation and Fibrosis during Progressive Renal Injury. PLoS ONE. 2009; 4（5）: e5704.
2. Monika Madan, Salomon Amar. Toll-Like Receptor-2 Mediates Diet and/or Pathogen Associated Atherosclerosis: Proteomic Findings. PLoS ONE. 2008; 3（9）: e3204.
3. Carsten J Kirschning, Stefan Dreher, Björn Maaß, Sylvia Fichte, Jutta Schade, Mario Köster, Andreas Noack, Werner Lindenmaier, Hermann Wagner, Thomas Böldicke. Generation of anti-TLR2 intrabody mediating inhibition of macrophage surface TLR2 expression and TLR2-driven cell activation. BMC Biotechnol. 2010; 10: 31.
4. Roger P.M. Sutmuller, Martijn H.M.G.M. den Brok, Matthijs Kramer, Erik J. Bennink, Liza W.J. Toonen, Bart-Jan Kullberg, Leo A. Joosten, Shizuo Akira, Mihai G. Netea, Gosse J. Adema. Toll-like receptor 2 controls expansion and function of regulatory T cells. J Clin Invest. 2006 February 1; 116（2）: 485–494.
5. Jaklien C. Leemans, Loes M. Butter, Wilco P. C. Pulskens, Gwendoline J. D. Teske, Nike Claessen, Tom van der Poll, Sandrine Florquin. The Role of Toll-Like Receptor 2 in Inflammation and Fibrosis during Progressive Renal Injury. PLoS ONE. 2009; 4（5）: e5704.
訂購信息：
| 貨號(hào) | 名稱 | 產(chǎn)地 | 規(guī)格 | 報(bào)價(jià)/元 | 貨期 |
| IML-102 | TLR2/NF-kB/SEAP Stable Reporter Cell Line | imgenex | 1Vial | 18244 | 2-3周 |
