Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Sample type | Multiple, including plasma/serum, whole blood, tissue, cell culture, urine | |
Sample input volume |
| |
Yield |
| |
Elution volume | 50 µL | |
Total processing time | 1.5–2 hr total time (20 min hands-on time) | |
Reactions (rxn) | 96 rxn | |
Shipping Condition | Room Temperature | |
Kit contents: | Box 1 (store at -5 to -30°C):
| Box 2 (store at room temperature):
|
Cat. No. | A27828 |
Use this kit with KingFisher automation to extract and purify RNA. The kit is designed for both low- and high-throughput isolation of true total RNA that covers the full range of RNAs present in cells, from small RNAs such as microRNA, to noncoding RNA, messenger RNA, and ribosomal RNA.
Eliminate the headache of using “specialized” kits for each sample type by using a single solution with the MagMAX mirVana Total RNA Isolation Kit. Capable of processing a wide range of sample types, the kit is designed for both low- and high-throughput extraction of true total RNA. True total RNA includes the full range of RNAs present in cells such as microRNA, to noncoding RNA, messenger RNA or mRNA, and ribosomal RNA or rRNA. The phenol-free, magnetic bead format allows for automated RNA isolation workflows from the following samples:
MagMAX products are designed to provide consistent and dependable nucleic acid extraction using silica–magnetic particle technology. Magnetic beads offer many benefits for isolating RNA from cells, tissue, or whole blood, and viral RNA from cell-free samples.
Learn how to achieve rapid, quantitative isolation of total RNA in both manual and automated workflows with the MagMAX mirVana Total RNA Isolation Kit.
Application Notes that support performance data associated with the MagMAX mirVana Total RNA Isolation kit.
Figure 1. RNA quality on the Agilent Bioanalyzer. Total RNA, including small RNA, was isolated from 6 different tissue types (A: Mouse Brain; B: Mouse Heart; C: Mouse Liver; D: Mouse Spleen; E: HeLa cells; and F: Jurkat cells) using two different isolations methods and kits. Results shown in blue are for RNA isolated using the mirVana miRNA Isolation Kit and results shown in red are for RNA isolated using the MagMAX-96 mirVana Total RNA Isolation Kit that provides equivalent or improved results.
Figure 2. qRT-PCR results for tissue and cells. Total RNA, including small RNA, was isolated from mouse tissue and cells using the mirVana miRNA Isolation Kit or the MagMAX-96 mirVana Total RNA Isolation Kit. For the MagMAX-96 mirVana kit, RNA was isolated manually or using one of our automated instruments (MagMAX Express-96, KingFisher-Flex, or KingFisher-Duo).
For qRT-PCR analylsis, cDNA was generated using equal volumes RNA input from each sample (diluted 1:10 for miRNA) and the High-Capacity cDNA Reverse Transcription Kit for mRNA and the TaqMan MicroRNA Reverse Transcription Kit and specific primers for miRNA. qPCR reactions were then performed on 2 µL of cDNA using specific TaqMan Assays and TaqMan Universal Master Mix II (no UNG). Ct values were averaged and then graphed by target.
Figure 3. Results with TaqMan Advanced miRNA System. Total RNA, including small RNA, was isolated from mouse liver, HeLa cells, and human plasma using the mirVana miRNA Isolation Kit, mirVana PARIS miRNA Isolation Kit, or MagMAX-96 mirVana Total RNA Isolation Kit.
For qRT-PCR analylsis, cDNA was generated using equal volumes RNA input from each sample (diluted 1:10 for liver and HeLa) and the TaqMan Advanced cDNA Synthesis Kit and protocol. qPCR reactions were then performed on 2 µL of cDNA using the specific TaqMan Advanced miRNA Assays and TaqMan FAST Advanced Master Mix and fast cycling conditions. Ct values were averaged and then graphed by target.
Figure 4. qRT-PCR results for biofluids. Total RNA, including small RNA, was isolated from serum, plasma, and urine using the mirVana PARIS kit or the MagMAX-96 mirVana Total RNA Isolation Kit. For the MagMAX-96 mirVana kit, RNA was isolated manually or using one of our automated instruments (MagMAX Express-96, KingFisher-Flex, or KingFisher-Duo).
For qRT-PCR analylsis, cDNA was generated using equal volumes RNA input from each sample and the High-Capacity cDNA Reverse Transcription Kit for mRNA and the TaqMan MicroRNA Reverse Transcription Kit and specific primers for miRNA. qPCR reactions were then performed on 2 µL of cDNA using specific TaqMan Assays and TaqMan Universal Master Mix II (no UNG). Ct values were averaged and then graphed by target.
Sample type | Multiple, including plasma/serum, whole blood, tissue, cell culture, urine | |
Sample input volume |
| |
Yield |
| |
Elution volume | 50 µL | |
Total processing time | 1.5–2 hr total time (20 min hands-on time) | |
Reactions (rxn) | 96 rxn | |
Shipping Condition | Room Temperature | |
Kit contents: | Box 1 (store at -5 to -30°C):
| Box 2 (store at room temperature):
|
Cat. No. | A27828 |
Use this kit with KingFisher automation to extract and purify RNA. The kit is designed for both low- and high-throughput isolation of true total RNA that covers the full range of RNAs present in cells, from small RNAs such as microRNA, to noncoding RNA, messenger RNA, and ribosomal RNA.
Eliminate the headache of using “specialized” kits for each sample type by using a single solution with the MagMAX mirVana Total RNA Isolation Kit. Capable of processing a wide range of sample types, the kit is designed for both low- and high-throughput extraction of true total RNA. True total RNA includes the full range of RNAs present in cells such as microRNA, to noncoding RNA, messenger RNA or mRNA, and ribosomal RNA or rRNA. The phenol-free, magnetic bead format allows for automated RNA isolation workflows from the following samples:
MagMAX products are designed to provide consistent and dependable nucleic acid extraction using silica–magnetic particle technology. Magnetic beads offer many benefits for isolating RNA from cells, tissue, or whole blood, and viral RNA from cell-free samples.
Learn how to achieve rapid, quantitative isolation of total RNA in both manual and automated workflows with the MagMAX mirVana Total RNA Isolation Kit.
Application Notes that support performance data associated with the MagMAX mirVana Total RNA Isolation kit.
Figure 1. RNA quality on the Agilent Bioanalyzer. Total RNA, including small RNA, was isolated from 6 different tissue types (A: Mouse Brain; B: Mouse Heart; C: Mouse Liver; D: Mouse Spleen; E: HeLa cells; and F: Jurkat cells) using two different isolations methods and kits. Results shown in blue are for RNA isolated using the mirVana miRNA Isolation Kit and results shown in red are for RNA isolated using the MagMAX-96 mirVana Total RNA Isolation Kit that provides equivalent or improved results.
Figure 2. qRT-PCR results for tissue and cells. Total RNA, including small RNA, was isolated from mouse tissue and cells using the mirVana miRNA Isolation Kit or the MagMAX-96 mirVana Total RNA Isolation Kit. For the MagMAX-96 mirVana kit, RNA was isolated manually or using one of our automated instruments (MagMAX Express-96, KingFisher-Flex, or KingFisher-Duo).
For qRT-PCR analylsis, cDNA was generated using equal volumes RNA input from each sample (diluted 1:10 for miRNA) and the High-Capacity cDNA Reverse Transcription Kit for mRNA and the TaqMan MicroRNA Reverse Transcription Kit and specific primers for miRNA. qPCR reactions were then performed on 2 µL of cDNA using specific TaqMan Assays and TaqMan Universal Master Mix II (no UNG). Ct values were averaged and then graphed by target.
Figure 3. Results with TaqMan Advanced miRNA System. Total RNA, including small RNA, was isolated from mouse liver, HeLa cells, and human plasma using the mirVana miRNA Isolation Kit, mirVana PARIS miRNA Isolation Kit, or MagMAX-96 mirVana Total RNA Isolation Kit.
For qRT-PCR analylsis, cDNA was generated using equal volumes RNA input from each sample (diluted 1:10 for liver and HeLa) and the TaqMan Advanced cDNA Synthesis Kit and protocol. qPCR reactions were then performed on 2 µL of cDNA using the specific TaqMan Advanced miRNA Assays and TaqMan FAST Advanced Master Mix and fast cycling conditions. Ct values were averaged and then graphed by target.
Figure 4. qRT-PCR results for biofluids. Total RNA, including small RNA, was isolated from serum, plasma, and urine using the mirVana PARIS kit or the MagMAX-96 mirVana Total RNA Isolation Kit. For the MagMAX-96 mirVana kit, RNA was isolated manually or using one of our automated instruments (MagMAX Express-96, KingFisher-Flex, or KingFisher-Duo).
For qRT-PCR analylsis, cDNA was generated using equal volumes RNA input from each sample and the High-Capacity cDNA Reverse Transcription Kit for mRNA and the TaqMan MicroRNA Reverse Transcription Kit and specific primers for miRNA. qPCR reactions were then performed on 2 µL of cDNA using specific TaqMan Assays and TaqMan Universal Master Mix II (no UNG). Ct values were averaged and then graphed by target.
Just like all Applied Biosystems MagMAX kits, the mirVana total RNA isolation kits are optimized for KingFisher instruments.
Nucleic Acid Purification and Analysis Support Center
Find tips, troubleshooting help, and resources for your nucleic acid purification & analysis applications.
For Research Use Only. Not for use in diagnostic procedures.