Animal Total RNA Isolation Kit Total RNA Extraction And Purification Kit For Animal Tissues & Cell

Animal Total RNA Isolation Kit Total RNA Extraction And Purification Kit For Animal Tissues & Cell

Catalog Number:
NAPK456071FOR
Mfr. No.:
RE-03011/03014
Price:
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      • Overview
        • Quickly and efficiently extract high-purity and high-quality total RNA from various animal tissues.
          • No need to worry about RNA degradation; the whole system is RNase-Free.
          • Effectively remove DNA-using DNA-Cleaning Column.
          • Remove DNA without adding DNase.
          • Simple-all operations are completed at room temperature.
          • Fast -operation can be completed in 30 minutes.
          • Safe-no organic reagent required.
          • High purity -OD260/280=1.8-2.1.

          Please contact us at for specific academic pricing.

          Background

          This kit uses the spin column and formula developed by our company, which can extract high-purity and high-quality total RNA from various animal tissues with high efficiency.It provides an efficient DNA-Cleaning Column, which can easily separate and adsorb genomic DNA from the supernatant and tissue lysate, simple and time-saving; RNA-only Column can efficiently bind RNA and can be processed simultaneously with a unique formula Lots of samples.
          The whole system is RNase-Free, so that the extracted RNA is not degraded; Buffer RW1, Buffer RW2 buffer washing system, so that the obtained RNA is free of protein, DNA, ion, and organic compound pollution.

      • Properties
        • Storage
          The kit can be stored for 24 months at room temperature (15-25°C) or 2-8°C for longer time. Buffer RL1 can be stored at 4°C for 1 month after adding β-mercaptoethanol (optional).

          * For research use only.

      • Applications
        • Application Description
          It is suitable for the extraction and purification of total RNA from a variety of fresh or frozen animal tissues or cultured cells.
      • Reference
        • 1. IF:18.808: Zheng, Q., Qin, F., Luo, R., et al. mRNA-Loaded Lipid-Like Nanoparticles for Liver Base Editing Via the Optimization of Central Composite Design. Adv. Funct. Mater. 2021, 31, 2011068.doi:10.1002/adfm.202011068.
          2. IF:18.187:He X, Hong W, Yang J, et al. Spontaneous apoptosis of cells in therapeutic stem cell preparation exert immunomodulatory effects through release of phosphatidylserine. Signal Transduct Target Ther. 2021 Jul 14;6(1):270. doi: 10.1038/s41392-021-00688-z.
          3. IF:17.97:Dai Z, Liu H, Liao J, et al. N7-Methylguanosine tRNA modification enhances oncogenic mRNA translation and promotes intrahepatic cholangiocarcinoma progression. Mol Cell. 2021 Jul 29:S1097-2765(21)00555-4. doi: 10.1016/j.molcel.2021.07.003.
          4. IF:9.225:Cao X, Shu Y, Chen Y, et al. Mettl14-Mediated m6A Modification Facilitates Liver Regeneration by Maintaining Endoplasmic Reticulum Homeostasis. Cell Mol Gastroenterol Hepatol. 2021;12(2):633-651. doi: 10.1016/j.jcmgh.2021.04.001.

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