mirror of
https://github.com/scinote-eln/scinote-web.git
synced 2024-09-21 23:46:21 +08:00
917 lines
39 KiB
JSON
917 lines
39 KiB
JSON
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"name": "Development of SNP markers panel",
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||
"last_modified_by_id": null,
|
||
"position": 3
|
||
},
|
||
{
|
||
"id": 3947,
|
||
"text": "Carefully decant away the supernatant and wash the DNA pellet with 3 mL of 70% ethanol.",
|
||
"checked": false,
|
||
"checklist_id": 959,
|
||
"created_at": "2018-12-21T09:54:21.522Z",
|
||
"updated_at": "2018-12-21T09:54:21.522Z",
|
||
"created_by_id": null,
|
||
"last_modified_by_id": null,
|
||
"position": 4
|
||
},
|
||
{
|
||
"id": 3948,
|
||
"text": "Gently swirl the solution and centrifuge again for 10 min at 5000 × g.",
|
||
"checked": false,
|
||
"checklist_id": 959,
|
||
"created_at": "2018-12-21T09:54:21.529Z",
|
||
"updated_at": "2018-12-21T09:54:21.529Z",
|
||
"created_by_id": null,
|
||
"last_modified_by_id": null,
|
||
"position": 5
|
||
},
|
||
{
|
||
"id": 3949,
|
||
"text": "Carefully decant the supernatant and air-dry DNA pellet for 15 min at room temperature. Once dried, suspend DNA in 200 μL of TE buffer.",
|
||
"checked": false,
|
||
"checklist_id": 959,
|
||
"created_at": "2018-12-21T09:54:21.535Z",
|
||
"updated_at": "2018-12-21T09:54:21.535Z",
|
||
"created_by_id": null,
|
||
"last_modified_by_id": null,
|
||
"position": 6
|
||
}
|
||
]
|
||
}
|
||
],
|
||
"step_comments": [],
|
||
"step_assets": [],
|
||
"assets": [],
|
||
"step_tables": [],
|
||
"tables": []
|
||
}
|
||
]
|
||
}
|
||
],
|
||
"results": []
|
||
}
|
||
],
|
||
"my_module_groups": [
|
||
{
|
||
"id": 1167,
|
||
"created_at": "2018-12-17T07:51:25.142Z",
|
||
"updated_at": "2018-12-17T07:51:25.142Z",
|
||
"created_by_id": 202,
|
||
"experiment_id": 433
|
||
}
|
||
]
|
||
}
|