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1. mRNA sequencing
mRNA sequencing enables profiling of all mRNAs transcripted from cells under specific conditions. It is a powerful technology for revealing gene expression profile, gene structures and molecular mechanisms of certain biological processes. To date, mRNA sequencing has been widely employed in fundamental research, clinical diagnostics, drug development, etc.
Sample requirement:
Library Type |
Sample Type |
Amount |
RNA Integrity Number |
Purity |
Eukaryotic RNA-Seq |
Total RNA |
≥ 0.5 μg |
≥ 6.8 (Animal), with smooth base line |
OD260/280 = 1.8-2.2; |
Total RNA (Blood) |
≥ 0.8 μg |
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Total RNA (Single Cell) |
≥ 100 ng |
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Amplified cDNA (double-stranded) |
≥ 100 ng |
Fragments between 400bp and 5000bp with main peak at ~2000bp |
OD260/280 = 1.8-2.0; |
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Eukaryotic RNA-Seq |
Total RNA |
≥ 0.8 μg |
≥ 6.8 (Animal), with smooth base line |
OD260/280 = 1.8-2.2; |
2. Long non-coding RNA sequencing
Long non-coding RNA sequencing service (lncRNA-seq) is a comprehensive next-generation method to detect the transcripts with a length of over 200nt, which do not encode protein and perform as regulatory elements in multiple biological processes. However, the progressive library preparation enables information enrichment and gene expression profiling for both coding and non-coding transcripts from a high-sensitive transcriptomic perspective. Bioinformatic analysis does not reveals the quantification and functional enrichment of the target transcripts, but also indicates the strand orientation and regulatory relation of lncRNA targeted mRNA.
Sample requirement:
Library Type |
Sample Type |
Amount |
RNA Integrity Number |
Purity |
lncRNA Library |
Total RNA |
≥ 2ug |
Animal ≥ 6.5, Plant ≥ 6, with smooth baseline |
OD260/280 = 1.8-2.2; |
Exosomal lncRNA Library |
Exosomal RNA |
≥ 20ng |
Peak between 25-200nt, FU> 10, no peak > 2000nt |
3. Small RNA sequencing
Beibi Biology offers comprehensive Small RNA Sequencing service (sRNA-seq), to investigate the regulatory network of noncoding RNA of 18-40nt in length, especially for microRNA (miRNA) transcripts. Variations in miRNA can be correlated with gene silencing and post-transcriptional regulation of gene expression, which provides researchers an effective method of regulating target on mRNAs with unprecedented sensitivity and high resolution. Bioinformatic analysis of sRNA-seq illustrates differential expression of miRNAs, structural alterations and discovery of novel small RNAs via a high throughput research technique.
Library Type |
Sample Type |
Amount |
RNA Integrity Number |
Purity |
Small RNA Library |
Total RNA |
≥ 2 ug |
Animal ≥ 7.5, Plant ≥ 7, with smooth baseline; |
OD260/280 = 1.8-2.2; |
Exosomal Small RNA Library |
Exosomal RNA |
≥ 20ng |
Peak between 25-200nt, FU> 10, no peak > 2000nt |
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