Service Introduced: Clear the rRNA in the tissue sample, retain mRNA and other non-coding RNA, and then build a library for sequencing of the sample, after obtaining the sequencing data, you can analyze the transcript is from the righteous or antisense DNA strand, you can accurately count the local number of transcripts and confirm the structure of the gene, and you can find more antisense transcripts, providing a data basis for subsequent analytical research. Click to download the "Sequencing Service Application Form", fill in the form as required and send it to zhangxinshuang@ cibr.ac.cn.
Sample request:
RNA Library type |
Sample quality and total quantity requirements (single database construction) |
LncRNA |
M≥4μg, RIN≥6.8 (animals), 6.3 (plants, fungi), baseline flat (soft body, etc. without 28S species) |
Library type |
Sample type |
Deliver guide |
Chain-specific libraries |
Cell |
The tissue should not be less than 1-1.5g, frozen in liquid nitrogen |
Blood |
The number of cells was 7-8×107 |
|
Tissue |
Mammals ≥6ml |
|
Bacteria |
About 3 90mm plates /80mL of freshly cultured thalli |
Technical route:
Frequently asked questions:
Q: Why does the lncRNA library remove rRNA?
Some of the lncRNAs have polyA tails, some do not, in order to ensure that the full lncRNA can be obtained, it is not recommended to use oligodT-labeled magnetic beads for enrichment, it is recommended to use the method of removing ribosomal RNA.
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