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3Â¥2012-06-04 08:56:53
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Adherence assay
CHOK1 cells were grown in 24-well tissue culture plates to approximately 80% confluence. Cells were transfected with either pCMV5 Nrx1¦Â-mCherry or pCMV5 FLAG-Nrx1¦Â-mCherry using Lipofectamine 2000 (Invitrogen, Carlsbad, CA) according to the manufacturer's instructions and grown for 36 hours to allow for protein expression. For attachment assays, bacteria were washed 2 times in PBS, resuspended in CD CHO media and incubated for 1 h with CHOK1 cells at an MOI of 10. To remove unattached bacteria, cells were washed 4 times with PBS. To determine the number of attached bacteria, CHOK1 cells were lysed with sterile water and serial dilutions plated on the appropriate media. The number of attached bacteria was reported as a percent of total bacteria at the end of the incubation period. Each experiment was performed in triplicate wells and repeated three times. Statistical analysis was performed using the Student's t-test.

Adhesion assays
A549 cells (human alveolar type II pneumocytes; ATCC CRL-185), were grown to 90% confluence on 24-well plates (~106 cells/well). Prior to use, cells were washed with cell F12 media to remove serum. For competitive inhibition binding assays, A549 cells were incubated with 1?M of either rBR, rBR.C, a synthesized peptide corresponding to AA 122-167, or BSA for 1 HR. Following incubation, cells were exposed to media that contained 107 cfu/mL of bacteria and incubated for 1 h at 37¡ãC in 5% CO2. Nonadhering bacteria were removed by washing the cells 3 times with T-PBS and the number of adhering bacteria was determined by lysis of the monolayer with 0.1% Triton X-100 and plating wells per experiment.
4Â¥2012-06-04 09:35:29
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castlered

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4Â¥: Originally posted by xuzhengxin405 at 2012-06-04 09:35:29
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Adherence assay
CHOK1 cells were grown in 24-well tissue culture plates to approximately 80% confluence. Cells were transfected with either pCMV5 N ...

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xuzhengxin405

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5Â¥: Originally posted by castlered at 2012-06-04 14:51:43
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96liuh

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7Â¥2012-06-20 11:10:41
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dodou

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