--- author: Sam White toc-title: Contents toc-depth: 5 toc-location: left layout: post title: DNA Isolation and Quantification - C.bairdi Hemolymph Pellets in RNAlater date: '2020-01-17 14:46' tags: - Chionoecetes bairdi - Tanner crab - DNA - DNA isolation - DNA quantification - Qubit categories: - 2020 - Miscellaneous --- Isolated DNA from the following 23 samples: - 6128_112_9 - 6204_114_9 - 6141_123_9 - 6245_126_9 - 6240_134_9 - 6260_136_9 - 6257_138_9 - 6259_139_9 - 6258_140_9 - 6255_143_9 - 6256_146_9 - 6265_155_9 - 6266_156_9 - 6261_164_9 - 6120_165_9 - 6251_167_9 - 6262_168_9 - 6243_173_9 - 6263_179_9 - 6264_180_9 - 6200_208_12 - 6204_252_12 - 6190_256_12 Isolated DNA using the [Quick DNA/RNA Microprep Kit](https://github.com/RobertsLab/resources/blob/master/protocols/Commercial_Protocols/ZymoResearch_quick-dna-rna_microprep_plus_kit_20190411.pdf) (ZymoResearch; PDF) according to the manufacturer's protocol for liquids/cells in RNAlater. - Used 35uL from each RNAlater/hemocyte slurry. - Mixed with equal volume of H2O (35uL). - Retained DNA on the Zymo-Spin IC-XM columns for isolation after RNA isolation. - DNA was eluted in 15uL H2O DNA was quantified on the Roberts Lab Qubit 3.0 using the 1x DNA High Sensitivity Assay (Invitrogen), using 2uL of each sample. Two samples were too concentrated, so those two samples were re-quantified using 1uL of sample. --- # RESULTS Qubit results (Google Sheet): - [20200117_qubit_cbai_DNA](https://docs.google.com/spreadsheets/d/12pVDjM5EkiPHdcILZBhZsn9m4ftXfVy8SC5rUr9zySM/edit?usp=sharing) Got DNA from all samples, despite the fact that [I didn't get any RNA from them...](https://robertslab.github.io/sams-notebook/posts/2020/2020-01-17-RNA-Isolation-and-Quantification---C.bairdi-Hemolymph-Pellets-in-RNAlater/) Samples were stored at -80oC in: [Rack 6, 4, 1](http://b.link/srlab-80C) in [C.bairdi gDNA Box #1](https://docs.google.com/spreadsheets/d/1D09mPvwDReuUNR36p_BrlrNfev_Ko1F83W4EKdAO6bk/edit?usp=sharing)