By BLAST analysis, these sequences have no homology with other coding sequences in human. Scrambled sequence used as negative control: 5′-CGAGTAAGACCATTCA GGTC-3′. The 5′end of this sequence corresponds to the cut-off point for BamH I GSK126 cell line enzyme (GATCC), while the 3′end, containing the T6 sequence, BYL719 mw corresponds to the cutting site for

Hind III enzyme (AGCTT). A ring sequence of 9 base pairs exists between the sense and anti-sense strands (TTCAAGAGA). Construction of shRNA expression plasmid Two strands of oligonucleotides would undergo annealing, ligation, and transformation. To identify positive clones, the constructed shRNA expression plasmids were identified by sequencing in Takara Biotechnology Company. shRNA vectors were named pGenesil-CENPE 1, 2, 3 and pScramble (negative control) respectively. Real-time PCR analysis Total RNA were isolated from adherent cells and clinical samples using the TRIZOL reagent (Invitrogen). First-strand cDNA was synthesized from 0.5 μg of Luminespib cell line total RNA by using random hexamers. The primers

used for quantitating CENP-E mRNA were 5′-GCGATGGAAGAACAACTAGGTACC-3 ‘(forward) and 5′-GTTG CTTGGGACTGTAAAAGCTGT-3 ‘ (reverse) with a TaqMan-MGB(genecore, china) probe 5′(FAM)-AAAACGAGCACAGCGAAGAATAGCCAGAA-3′. Because CENP-E degradation kinetically follows the proteolysis of Cyclin B1 in anaphase, Cyclin B1 mRNA was used to normalize CENP-E mRNA, for which the primers and TaqMan-MGB probe were 5′-AGCACCTGGCTAAGAATG-3′(forward), 5′-CTTCGATGTGGCATACTTG-3′(reverse), and 5′(FAM) – ATCAAGGACTTACA AAGCACATG ACTGTC-3′. The PCR cycling program was 94°C for 5 minutes, then 40 cycles of 94°C for 30 seconds, 51°C for 30 seconds. Western Blotting For CENP-E protein level analysis, cells and tissues were lysed with RIPA lysis Buffer, supplemented with protease inhibitors. The TCL lysates were cleared

by centrifugation at 14,000 rpm for 30 min at 4°C and quantitated by Bradford Protein Assay. Protein was enriched by immunoprecipitation method, and the precipitates were boiled with SDS-loading buffer, separated on 40-120 g/L and 100 g/L SDS-PAGE respectively, and then transferred onto polyvinylidene difluoride membrane (Millipore). Thereafter, the membrane was probed with affinity-purified mouse monoclonal antibody against human CENP-E (Abcam, USA) and mouse monoclonal antibody of Cyclin B1(Abcam, USA), followed by horseradish peroxidase-conjugated secondary antibody. After washing, the membrane was incubated in ECL Plus reagent before detection. Then, the blots were scanned in grey scale and analyzed using QUANTITY ONE software. Immunofluorescence Microscopy LO2 cells were seeded onto sterile, acid-treated 12-mm coverslips in 24-well plates. Nocodazole-treated LO2 cells were applied to poly-L-lysine-coated coverslips.