I guess I will have to make my own. If I understood correctly, it seems quite doable:
http://www.plantphysiol.org/content/145/4/1129.full
From here, I need to make primers for the described integration target.
Add restriction sites.
Then I isolate some genetic material from chloroplasts (dirty) and put it into a PCR.
Make primers for KanamycinR.
Then fuse flankingsite - KanR - Lux - flankingsite into some plasmid. Ready (?)
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