Fig. 5.
![Fig. 5. Immunoprecipitation experiment with Ki-S2 on L428 cells after the cells were labeled with [32P]orthophosphate (A). In lane B, L428 cells were arrested with colcemid (0.15 μg/mL) overnight before labeling with [32P]. (C) Isotype control experiment. Molecular weight standards are shown on the right (in kilodaltons).](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/90/1/10.1182_blood.v90.1.226/5/bl_0002f5.jpeg?Expires=1722813387&Signature=aLrZb5UiWuVBEopN7Y5qVT7-XSI30Lpet0MPDbtKxsKwMr0cdfrRL3JkNBgyBymMq3Zmw9vFe45rJ7~LJdeAYcSMUZLIJvJfKDU1186amQlR-m0c5L1lbZhKKprUJQpuns2fxQ5Ar4xzWXJkSZt5OzaYynzLqbZknpSvVdnsI449RciuXnPJtSonp3knuJa~40dgzxgjwl2LwUhRttosXigsdA5phaWCr1cekJnPAgWT-v8GqGXsY~kn5nBPTJHrRf8NmB~liIFgvikHcEEnIEcoYhjh2KISY-ipcTPvu19TDvppu1wYvaBaOssgwMe4Gt5xGzMpgLIdTaPbkY06oQ__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)
Immunoprecipitation experiment with Ki-S2 on L428 cells after the cells were labeled with [32P]orthophosphate (A). In lane B, L428 cells were arrested with colcemid (0.15 μg/mL) overnight before labeling with [32P]. (C) Isotype control experiment. Molecular weight standards are shown on the right (in kilodaltons).
