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YR23017 YALEPIC Animal Cell & Tissue Total RNA Fast Isolation Kit

YALEPIC® Animal Cell & Tissue Total RNA Rapid Isolation Kit

Maximum Yield, Minimum Noise — Reliable total RNA Isolation from animal cells and tissues via spin column

An optimized spin column workflow that turns animal cells and tissues into high-quality total RNA ready for downstream applications.

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YR23017 50T Online Consult +

Product Description

YALEPIC® Animal Cell & Tissue Total RNA Fast Isolation KitNo DNase Iprovides a rapid method for extracting total  RNA from animal tissues and cells. The kit is based on silica gel membrane purification technology  and does not require β-mercaptoethanol, phenol/chloroform, or any other toxic reagent during  the extraction process. It takes only 7 min to extract high-quality RNA. The kit contains Fast  gDNA Filter Columns which can effectively remove impurities and gDNA. FastPure RNA  Columns RT can efficiently bind RNA with an optimized buffer to obtain high-purity total RNA. The  isolated RNA has little gDNA residues and no proteins or other impurities contamination. It can  be used for RT-PCR, Real-Time PCR, Microarrarys and other downstream experiments.

Features

  • Fast: It only requires 7 min at room temperature.
  • Safer: No need for β-mercaptoethanol and phenol or chloroform.
  • Minimal gDNA residue: No need for on-membrane digestion with DNase I, one-step gDNA contamination removal.
  • High RNA purity: High purity of extracted RNA, which is ready for use in demanding downstream experiments.

Application

Tissue samples:10~30mg;

Cell:≤1×107

Storage

Transport at room temperature.

Store at 10 ~ 30°C for one year.

How many extractions can be performed with one YALEPIC Animal Cell/Tissue Total RNA Rapid Extraction Kit? Can it process both animal tissues and cells?

This is a standard 50T kit (catalog YR23017), providing 50 RNA extraction reactions. It is a universal tissue/cell RNA extraction kit suitable for both animal tissues (liver, spleen, kidney, brain, etc.; recommended 10-30 mg) and cultured cells (adherent/suspension; recommended up to 1×10^7 cells), eliminating the need for separate kits.

Which animal tissues can this kit extract RNA from? Are there restrictions on special tissues (spleen, kidney)?

Suitable for various common animal soft tissues including liver, spleen, kidney, brain, heart, skeletal muscle, and lung. Note: DNA-rich tissues (liver, spleen, kidney) should use no more than 10-20 mg to avoid affecting extraction and increasing gDNA residue risk.

How long does the RNA extraction process take? Does it require special equipment or low-temperature conditions?

The entire rapid RNA extraction process can be completed in 7 minutes at room temperature – from sample lysis to RNA elution, with no pre-cooled centrifuge or ice-bucket operation needed. All centrifugation is performed at room temperature (15-30 degrees C) using a standard benchtop centrifuge (>=12,000 rpm). This 7-minute room-temperature extraction is a core advantage, compared to traditional TRIzol (~1.5 hours) and conventional column methods (~30 minutes).

Does the extraction process require chloroform or phenol? Is the operation safe?

Completely unnecessary. This product uses silica membrane column purification technology, with no chloroform, phenol, or beta-mercaptoethanol needed. This is very friendly for laboratory safety management and operator health, especially suitable for labs sensitive to organic reagents or with limited ventilation.

Is the RNA purity high enough for direct qPCR use?

Yes. The kit uses a dual-column filtration system – Fast gDNA Filter Columns effectively remove genomic DNA, combined with optimized wash buffers to remove protein and salt residues. Total RNA purity A260/A280 is typically 1.9-2.1, directly usable for RT-PCR, qPCR, Northern Blot, and other high-purity-requirement downstream experiments. For complete DNA removal (especially for low-abundance gene expression analysis), use RNase-free DNase I for on-column or post-elution digestion.

Can the kit remove genomic DNA (gDNA) contamination? What if gDNA residue persists?

Yes. The kit includes Fast gDNA Filter Columns for one-step efficient gDNA removal during extraction, with no additional steps needed. For DNA-rich samples (liver, spleen, kidney), keep starting amount to 10-20 mg. For highly DNA-sensitive downstream experiments (qPCR), use RNase-free DNase I for further digestion after RNA elution. Detailed instructions are in the protocol.

How should the kit be stored? Does transport require cold chain?

All components can be stored dry at 10-30 degrees C room temperature, no refrigeration or freezing needed. Transport at room temperature without cold chain support. This provides great convenience for laboratory inventory management and reduces transport/storage costs. After opening, store at room temperature until the kit expiry date (see bottle label), but avoid repeated opening that may introduce contamination.

How long is the kit effective after opening? Can it be repeatedly opened and used?

All components are designed for stability throughout the shelf life (typically 12-24 months, see bottle label). Tighten caps after each use and store in a clean, dry room temperature environment. Avoid prolonged exposure of lysis and wash buffers to air to prevent solvent evaporation or RNase contamination. No freeze-thaw needed (all components stored at room temperature).

What if column clogging or centrifugation difficulty occurs?

Column clogging is typically caused by: (1) Excessive sample input – refer to recommended amounts (tissue 10-30 mg, cells up to 1×10^7); (2) Insufficient grinding/lysis – grind thoroughly, increase lysis buffer volume and extend lysis time if needed. Do not aspirate precipitate when transferring supernatant to the column. See the troubleshooting section in the protocol for a complete guide.

What to do if RNA yield is low?

Low RNA yield may be caused by: insufficient sample (increase amount, but tissue <30 mg, cells <1x10^7); sample degradation from improper storage (use fresh or liquid nitrogen flash-frozen samples at -85 to -65 degrees C, avoid freeze-thaw); insufficient grinding/homogenization (increase lysis buffer volume and time); insufficient elution (add RNase-free ddH2O to membrane center, reduce elution volume, pre-warm to 56 degrees C or extend room temperature incubation, or perform double elution).

What downstream experiments can the extracted RNA be used for?

The high-purity, high-integrity total RNA is suitable for RT-PCR, real-time quantitative PCR (qPCR/Real-Time RT-PCR), microarray analysis, Northern Blot, Dot Blot, Poly(A) RNA selection, in vitro translation, RNase protection assay, molecular cloning, and more. Products can be used directly or stored long-term at -85 to -65 degrees C.

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