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RNA Isolation Tri-Liquid

RNA Isolation Tri-Liquid is a reagent for the simple and efficient isolation of total RNA from different starting materials (tissue, cells, bacteria, viruses, plants, etc.). Extraction is carried out using a particularly time-saving one-step liquid-phase separation. With this method, RNA can be efficiently extracted from limited starting material with small tissue quantities and cell numbers (5 x 106) as well as from large quantities (tissue up to 100 mg and cells > 107).

Properties

Fast - preparation time: approx. 1 hour
Efficient - for both limited starting material and large quantities
Reliable - Extraction of high-quality, undegraded RNA
Reproducible - Free from DNA and protein contamination

Article list

ProductsArticle numberQuantityShop
RNA Isolation Tri-Liquid
BS67.211.0100
100 ml

Good to know

RNA Isolation Tri-Liquid contains a mixture of phenol and guanidinisothiocyanate in a monophasic solution. After the addition of chloroform and subsequent centrifugation, the homogenate separates into three phases, a colored lower organic phase, a whitish interphase and an upper colorless aqueous phase. The RNA is located in the upper aqueous phase. The RNA is precipitated from this aqueous phase by adding alcohol.

Extraction_method_RNA_Tri-Liquid_reagent_from_BioSELL.jpeg

RNA extraction with RNA Isolation Tri-Liquid can be performed in approx. 1 hour. The RNA extracted is ungraded and of high quality. It can be used for a variety of downstream applications, such as Northern analyses, cDNA synthesis, RT-PCR reactions, dot-blot hybridizations, poly(A)+ selections, in vitro translations, cloning and RNase assays.

Product information

Category:
RNA Isolation
Product type:
RNA Tri-Liquid reagent
Extraction method:
one-step liquid-phase separation
Form:
Liquid (pink)

Application

  • Northern analysis
  • cDNA synthesis
  • RT-PCR reactions
  • in vitro translations
  • Cloning
  • RNase assays
  • Dot-blot hybridizations
  • Poly(A)+ selections

Publications

Stabilizing a mammalian RNA thermometer confers neuroprotection in subarachnoid hemorrhage

Min Zhang, Bin Zhang, Chengli Liu, Marco Preußner, Megha Ayachit, Weiming Li, Yafei Huang, Deyi Liu, Quanwei He, Ann-Kathrin Emmerichs, Stefan Meinke, Shu Chen, LinWang, Liduan Zheng, Qiubai Li, QinHuang, Tom Haltenhof, Ruoxi Gao, Xianan Qin, Aifang Cheng, Tianzi Wei, Li Yu, Mario Schubert, Xin Gao, Mingchang Li, Florian Heyd
Nature Communications ( 2025) 16: 8319

Cross-presenting Langerhans cells are required for the early reactivation of resident CD8+ memory T cells in the epidermis

Nadine Kamenjarin, Katrin Hodapp, Felix Melchior, Gregory Harms, Ann-Kathrin Hartmann, Joschka Bartneck, Sabine Muth, Verena K. Raker, Christian Becker, Anna Brand, Björn E. Clausen, Markus P. Radsak, Hansjörg Schild, Hans Christian Probsta
PNAS (2023) 120: 34

Neutrophil extracellular traps and their histones promote Th17 cell differentiation directly via TLR2

Alicia S. Wilson, Katrina L. Randall, Jessica A. Pettitt, Julia I. Ellyard, Antje Blumenthal, Anselm Enders, Benjamin J. Quah, Tobias Bopp, Christopher R. Parish, Anne Brüstle
Nat Commun. (2022) 13: 528

Recruitment of a splicing factor to the nuclear lamina for its inactivation

Karen Vester, Marco Preußner, Nicole Holton, Suihan Feng, Carsten Schultz, Florian Heyd, Markus C. Wahl
Communications biology (2022) 5:736

Base editing repairs an SGCA mutation in human primary muscle stem cells

Helena Escobar, Anne Krause, Sandra Keiper, Janine Kieshauer, Stefanie Müthel, Manuel García de Paredes, Eric Metzler, Ralf Kühn, Florian Heyd, Simone Spuler
JCI Insight. (2021); 6(10):e145994

Increased versatility despite reduced molecular complexity: evolution, structure and function of metazoan splicing factor PRPF39

Francesca De Bortoli, Alexander Neumann, Ana Kotte, Bernd Timmermann, Thomas Schüler, Markus C. Wahl, Bernhard Loll, Florian Heyd
Nucleic Acids Research (2019) 47: 11; 5867–5879