Exosome RNA QC Kit
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AC25L51210 T980
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AC25L513100 T2880
- Product Description
- Product FAQ
- COA
- Product Literature
- MSDS
- Operation video
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Product Description
This product is an exosome RNA quality‑control kit, suitable for quality control of exosomal RNA derived from human, mouse, and rat sources. Because exosomes contain RNA molecules, this kit can also be used for exosome characterization, enabling the assessment of exosome quality and purity.
This product involves reverse transcription of exosomal RNA, followed by quantitative PCR detection using the SYBR Green I fluorescence method. Extensive research has identified two positive exosomal RNA targets (QC Assay A1 and B1, which are amplification primers for positive RNA targets) and one negative control target (QC Assay C1, an amplification primer used to detect bacterial contamination), all of which are employed to assess the quality of exosomal RNA.
This kit employs a highly efficient third-generation RT enzyme and Hotstart Taq DNA polymerase, effectively suppressing non-specific reactions and enabling accurate quantification over a broader range. Real-time detection of amplification products significantly enhances assay sensitivity, while eliminating the need for post-PCR gel electrophoresis, making it ideally suited for the analysis of exosomal RNA.
Order Information
Product Name
Item number
Specifications
Exosome RNA QC Kit
AC25L512
10T
Exosome RNA QC Kit
AC25L513
100T
Product ingredients
Component
AC25L512
AC25L513
A. RT Enzyme Mix (10×)
20 μL
200 μL
B. RT Reaction Buffer (2×)
100 μL
1mL
C. SYBR Green Fast qPCR Mix (2×)
600 μL
6×1 mL
D. dNTPs (10mM each)
10 μL
100 μL
E. QC RT Primers
10 μL
100 μL
F. QC Assay A1
20 μL
200 μL
G. QC Assay B1
20 μL
200 μL
H. QC Assay C1
20 μL
200 μL
I. DEPC-treated Water
1.25 mL
2×1.25 mL
Transportation and Storage
Blue Ice Transport. Store at -20°C away from light; shelf life: 12 months.
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This product is intended solely for scientific research and must not be used for clinical diagnosis, treatment, or any other purposes.
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Q: What are the sizes of the amplicons generated by primers A, B, and C?
A: A detects small RNA fragments of 60–70 bp, B detects mRNA of 300–400 bp, and C detects bacterial RNA of 200–300 bp.
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