| Size | 2 Plate Kit, 4 Plate Kit, 6 Plate Kit |
| Estimated Lead Time | 1-2 business days |
| Species | Human |
| Compatible Sample Types | Extracted RNA |
| Quantitative/Semi-Quantitative | Quantitative |
| Method Of Detection | Real-Time RT-PCR |
| Research Area | Epigenetics, RNA/DNA Modification |
| Shipping Type | Dry ice (additional shipping fee) |
| Storage | -20°C |
Format selection is based on the plate type compatible with your instrument model. Below are the compatible instruments for each plate type.
| Plate Type A (Cat: PCAH-RNAM-A) |
Plate Type B (Cat: PCAH-RNAM-B) |
Plate Type C (Cat: PCAH-RNAM-C) |
|---|---|---|
| ABI 5700 | ABI 7500 Fast | Roche Lightcycler 96 |
| ABI 7000 | ABI 7900 HT Fast | Roche Lightcycler 480 (96-well) |
| ABI 7300 | ABI StepOnePlus | Â |
| ABI 7500 | ABI ViiA 7 Fast | Â |
| ABI 7700 | Bio-Rad CFX Connect | Â |
| ABI 7900 HT | Bio-Rad CFX96 | Â |
| ABI QuantStudio 3, 5, 6 and 7 | Bio-Rad DNA Engine Opticon 2 | Â |
| ABI ViiA 7 | Stratagene MX4000 | Â |
| Bio-Rad Chromo4 | Â | Â |
| Bio-Rad iCycler | Â | Â |
| Bio-Rad iQ5 | Â | Â |
| Bio-Rad MyiQ | Â | Â |
| Bio-Rad MyiQ2 | Â | Â |
| Eppendorf Mastercycler EP Realplex 2 | Â | Â |
| Eppendorf Mastercycler EP Realplex 4 | Â | Â |
| Stratagene MX3000P | Â | Â |
| Stratagene MX3005P | Â | Â |
Recent discoveries in RNA modification–mediated gene regulation have fueled the rapidly expanding field of epitranscriptomics. Messenger RNAs (mRNAs), along with transfer RNAs (tRNAs) and ribosomal RNAs (rRNAs), undergo dynamic internal modifications such as N1-methyladenosine (m1A), N6-methyladenosine (m6A), N7-methylguanosine (m7G), 5-methylcytosine (m5C), N4-acetylcytidine (ac4C), adenosine-to-inosine (A-to-I), and pseudouridine (Ψ). These chemical marks serve as critical regulators of RNA stability, processing, translation, and overall metabolism. The deposition, removal, and recognition of RNA methylation are carried out by three major classes of proteins: "writers" (methyltransferases), "erasers" (demethylases), and "readers" (RNA-binding proteins). Increasing evidence links dysregulation of these regulators to a broad spectrum of human diseases and disorders.
The RayBio® Human RNA Modification qPCR Array is a SYBR Green-based qPCR assay that enables simultaneous profiling of 90 validated regulators across nine classes of RNA epitranscriptomic modifications. This kit contains six controls: three reference genes (internal control, INC) for data normalization, a genomic DNA (gDNA) control (GDC) for detection of possible gDNA contamination, a positive control (PC) for PCR amplification confirmation, and a negative control (NC) to monitor DNA contamination during workflow. Each 96-well plate is preloaded with a rigorously validated, highly specific primer pair to ensure consistent and reliable results. Simply add cDNA and qPCR master mix, run the assay, and analyze the expression profiles to uncover differentially expressed genes. Delivering high-quality results in as little as two hours, this PCR Array provides a rapid, convenient, and powerful tool for exploring the dynamic regulatory landscape of the epitranscriptome.
| Component | Description |
|---|---|
| 96-Well Array Plate | 96-well PCR plate with 2 µL paired primers in each well |
| qPCR Master Mix | qPCR master mix with Hot Start Taq |
| 96-Well Plate Sealing Film | Microplate adhesive sealing film |
Contact our technical support team for questions about compatibility: techsupport@raybiotech.com
The kit can be stored at -20°C for a period of 24 months prior to opening. Avoid repeated freeze-thaw cycles.
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Human RNA Modification qPCR Array
Human RNA Modification qPCR Array