TRIpure Total RNA Extraction Reagent

SKU:BHT15200027
Research Validated
Overview
Click light‑blue chips for details
TRIpure Total RNA Extraction Reagent is an extraction reagent from ELK Biotechnology. Single-reagent solution that lyses animal, plant and bacterial samples and recovers intact total RNA within 1 h.
Product Type Extraction Reagents
Sample Type Animal, plant and bacterial samples
Format Single-component liquid reagent
Purity OD260/OD280 1.9–2.2
Storage 4°C, protect from light
Shelf Life 1 year
Grade Research Use Only
Options selector
Catalog no. Size
EP013-100ML 100 mL
EP013-250ML 250 mL
EP013-100MLX10 100 mL x 10
EP013-250MLX40 250 mL x 40
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 100 mL, 250 mL, 100 mL x 10, 250 mL x 40
  • Lead time: options listed in "Availability Content"; other statuses may take longer.
  • Storage: 4°C, protect from light (shelf life 1 year)
  • Shipping: Ice bag transportation.
  • Upon receipt: refrigerate immediately and protect from light.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Applications
  • Nucleic Acid Isolation
Storage 4°C, protect from light
Shelf life 1 year
Shipping Ice bag transportation
Catalog no. (Mfr.) EP013
Main SKU BHT15200027
Extraction Reagents

Product Overview

TRIpure Total RNA Extraction Reagent is a reagent for total RNA extraction from various animal and plant, bacterial tissues/cells. It lyses cells and tissue rapidly and keeps the RNA in the sample intact, effectively inhibiting RNA degradation. The sample is lysed completely in the reagent. After centrifugation with chloroform, the solution forms a supernatant layer, an intermediate layer and an organic layer (lower pink layer). The RNA is distributed in the upper aqueous phase, and the supernatant layer is collected. Total RNA is recovered by isopropanol precipitation. The extracted total RNA is of high purity, with low protein and genomic DNA carryover. It can be directly used for Northern, dot hybridization, mRNA purification, in vitro translation, RT-PCR, poly(A)+ selection, RNase protection analysis, and construction of cDNA libraries and a variety of other molecular biology experiments.

TRIpure is a phenol-based reagent. One mL of TRIpure handles adherent cells from a 10 cm² culture area, 5×10⁶–1×10⁷ suspended cells, 10⁷ bacteria, 200 µL whole blood, 30–100 mg animal tissue or 50–100 mg plant tissue. The upper aqueous layer recovered after chloroform separation is about 50–60% of the total amount of added TRIpure. For pure RNA the OD260/OD280 ratio is between 1.9 and 2.2. Chloroform, isopropyl alcohol, 75% ethanol (DEPC water), DEPC and RNase-free equipment are supplied by the user. Per sample, 300 µL of chloroform is added and shaken for 15 s, the phases are separated by centrifugation at 12,000 rpm, the aqueous phase is precipitated with an equal volume of isopropanol at -20°C for 20 min, and the RNA pellet is washed with 75% ethanol and air-dried for 2–3 min.

Specifications

Format Single-component phenol-based liquid extraction reagent
Sample types Animal, plant and bacterial tissues and cells
Sample input per 1 mL reagent Adherent cells from 10 cm² culture area, 5×10⁶–1×10⁷ suspended cells, 10⁷ bacteria, 200 µL whole blood, 30–100 mg animal tissue or 50–100 mg plant tissue
Purity (OD260/OD280) Between 1.9 and 2.2 for pure RNA
Aqueous phase recovered About 50–60% of the TRIpure volume added
Processing time Total RNA extracted within 1 h

Applications

  • Total RNA extraction from animal, plant and bacterial tissues and cells
  • RNA extraction from virus and other trace samples
  • Northern blotting and dot hybridization
  • RT-PCR and in vitro translation
  • mRNA purification, poly(A)+ selection and cDNA library construction

Key Features

  • High extraction quality: Total RNA with high yield, high purity and good integrity can be extracted within 1 h.
  • Colored indicator: a dye turns the lower layer pink after centrifugal layering, so the upper aqueous phase is easy to remove.
  • High sensitivity: Higher extraction efficiency for the extraction of virus and other trace samples.
  • Flexible sample handling capacity: It has a good lysis effect on a small amount of tissue (50–100 mg) and cells (5×10⁶) and a large number of tissues (≥1 g) and cells (>10⁷).

Storage & Handling

The reagent is stored at 4°C in the dark and is valid for 1 year. RNA precipitated in 75% ethanol keeps at 4°C for 1 week or at -20°C for 1 year. Shipping: Ice bag transportation.

Usage Notes

  • Phenol is toxic and corrosive; handle in a fume hood with gloves and eye protection.
  • Use RNase-free equipment throughout the procedure.
  • Wear gloves, protective clothing and a mask, and avoid talking during the operation.
  • The RNA half-life is relatively short and RNA is easy to degrade.
  • Store the RNA precipitate in 75% ethanol at 4°C for up to 1 week or at -20°C for up to 1 year.

Safety & Regulatory

For research use only. Not intended for clinical, diagnostic or therapeutic use. Follow the manufacturer's manual and standard laboratory safety practice.

GradeResearch Use Only
ManufacturerELK Biotechnology
Catalog No.EP013
BioHippo SKUBHT15200027
Q.How should TRIpure Total RNA Extraction Reagent be stored and how long is it valid?
A.The reagent is stored at 4°C in the dark and is valid for 1 year. It is transported with an ice bag. RNA precipitated in 75% ethanol can be kept at 4°C for 1 week or at -20°C for 1 year.
Q.What is supplied and what has to be provided separately?
A.The product is a single extraction reagent supplied in 100 mL and 250 mL packs. Chloroform, isopropyl alcohol, 75% ethanol (DEPC water), DEPC and RNase-free equipment are supplied by the user.
Q.How much sample does 1 mL of TRIpure handle?
A.Per 1 mL of reagent: adherent cells from a 10 cm² culture area, 5×10⁶–1×10⁷ suspended cells, 10⁷ bacteria, 200 µL whole blood, 30–100 mg animal tissue or 50–100 mg plant tissue.
Q.What RNA purity can be expected?
A.For pure RNA the OD260/OD280 ratio is between 1.9 and 2.2. The extracted total RNA is of high purity, with low protein and genomic DNA carryover.
Q.What handling precautions apply?
A.Phenol is toxic and corrosive and should be handled in a fume hood with gloves and eye protection. RNase-free equipment should be used, with gloves, protective clothing and a mask, and talking during the operation should be avoided. The RNA half-life is relatively short and RNA is easy to degrade.
Q.Is this product for research use only?
A.Yes. The manual states that the product is for research use only.

Customization & Add-ons: Need this molecular biology reagent tailored to your workflow? We can help with bulk or custom pack sizes, alternative formats (spin column, magnetic bead or reagent-only kits; premixed or stand-alone reference dye), matched extraction, cDNA synthesis and qPCR workflows, and sourcing of related enzymes, ladders and consumables not in our catalog. Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services — our team will follow up with feasibility details and next steps.

Engineered exosomes enriched in netrin-1 modRNA promote axonal growth in spinal cord injury by attenuating inflammation and pyroptosis. Biomaterials Research, 2023. 10.1186/s40824-023-00339-0

Cell-Free Extracts from Human Fat Tissue with a Hyaluronan-Based Hydrogel Attenuate Inflammation in a Spinal Cord Injury Model through M2 Microglia/Microphage Polarization. Small, 2022. 10.1002/smll.202107838

Exosome-loaded methacrylated silk fibroin hydrogel delays intervertebral disc degeneration by DKK2-mediated mitochondrial unfolded protein response. Chemical Engineering Journal, 2025. 10.1016/j.cej.2025.162191

Targeted delivery of stattic to pulmonary vascular smooth muscle cells ameliorates pulmonary arterial hypertension. Chemical Engineering Journal, 2026. 10.1016/j.cej.2026.176067

β-catenin Activation Reprograms Ammonia Metabolism to Promote Senescence Resistance in Hepatocellular Carcinoma. Cancer Research, 2024. 10.1158/0008-5472.CAN-23-0673

Prolonged anesthesia induces neuroinflammation and complement-mediated microglial synaptic elimination involved in neurocognitive dysfunction and anxiety-like behaviors. BMC Medicine, 2023. 10.1186/s12916-022-02705-6

Peripheral nerves modulate the peri-implant osteogenesis under type 2 diabetes through exosomes derived from schwann cells via miR-15b-5p/Txnip signaling axis. JOURNAL OF NANOBIOTECHNOLOGY, 2025. 10.1186/s12951-025-03160-0

MiR-144-5p, an exosomal miRNA from bone marrow-derived macrophage in type 2 diabetes, impairs bone fracture healing via targeting Smad1. Journal of Nanobiotechnology, 2021. 10.1186/s12951-021-00964-8

ROS-Responsive Injectable Hydrogel Loaded with SLC7A11-modRNA Inhibits Ferroptosis and Mitigates Intervertebral Disc Degeneration in Rats. Advanced Healthcare Materials, 2024. 10.1002/adhm.202401103

Preoperative neoadjuvant targeted therapy remodels intra-tumoral heterogeneity of clear-cell renal cell carcinoma and ferroptosis inhibition induces resistance progression. Cancer Letters, 2024. 10.1016/j.canlet.2024.216963

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