RNA Preparation and Purification
Norgen Biotek Corp Plant/Fungi Rna Purif. Kit
Norgen’s Plant/Fungi Total RNA Purification Kit provides a rapid method for the isolation and purification of total RNA, including virus and viroid RNA, from a wide range of plants. Total RNA can be purified from fresh or frozen plant tissues, plant cells or filamentous fungi samples using this kit. All sizes of RNA are purified, including microRNA (miRNA) . The procedure is rapid and convenient. The RNA is purified without the use of phenol or chloroform. The purified RNA is of the highest quality, and can be used in a number of downstream applications including real time PCR, reverse transcription PCR, Northern blotting, RNase protection and primer extension, and expression array assays. Norgen's Plant/Fungi Total RNA Purification Kit is also available in a 96-well format for high throughput applications. Purification with the 96-well plates can be performed using either a vacuum manifold or centrifugation.
Norgen Biotek Corp CYTOPLASMIC/NCLR RNA PURIF KIT
Cytoplasmic & Nuclear RNA Purification Kit,100 Preps
Epoch Life Science Inc GenCatch™ Total RNA Extraction System (250 preps) Uniquely formulated buffers, reinforced columns with collection tubes, along with protocols.
Provides a simple, fast and cost-effective method to purify total RNA from various starting materials (such as cultured cells, tissues, bacteria, yeast, etc.). Total RNA with a molecular size greater than 200 nucleotides (which excludes smaller RNA such as 5S and 5.8S RNA, and tRNA) can be isolated. Silica membrane technology. Up to 65 ug yield. 200 ul elution volume. No phenol/chloroform extraction nor ethanol precipitation required. Instructions for sample type listed in protocol. Used by labs around the world. 18 month shelf life.
New England Biolabs, Inc. NEBNext Multiplex Small RNA Library Prep Kit for Illumina Set 2 – 96 reactions
The novel NEBNext Small RNA workflow has been optimized to minimize adaptor-dimers while producing high-yield, high-diversity libraries. The NEBNext Small RNA Library Prep Set for Illumina (Set 1) includes adaptors and multiplex primers with 12 indices, to enable multiplexing.
Macherey-Nagel NucleoSpin RNA Columns, 250 columns
NucleoSpin RNA Columns (250) binding columns for the isolation of RNA pack of 250
Bioworld URINEEXFOLIATED CELL) RNA
URINE (EXFOLIATED CELL) RNA PURIFICATION KIT: For the rapid purification of total RNA (including microRNA) from exfoliated cells in urine. Isolate and detect total RNA from as little as 1 mL of urine; Provides high quality RNA for sensi...
Sigma Aldrich Fine Chemicals Biosciences GENELUTE MRNA MINIPREP KIT
NC3839332 GENELUTE MRNA MINIPREP KIT
System Biosciences LLC EXOGLOW-RNA EV LABELING KIT
Label EV membranes (465 nm excitation/635 nm emission) with a reagent specifically optimized for EV labeling.Specific—carefully developed to generate a robust signal specific for EV membranes, leading to very low levels of backgroundCompatible—delivers robust performance on EVs isolated using all methods tested—including ExoQuick®, ultracentrifugation, and column-based workflowsEasy-to-use—labeling protocol is quick and straightforwardPowerful—can be used with as little as 1 µg of EVs
New England Biolabs, Inc. G(5')ppp(5')A RNA Cap Structure Analog – 1 umol
The 5' terminal m7G cap present on most eukaryotic mRNAs promotes translation in vitro at the initiation level. For most RNAs, elimination of the cap structure causes a loss of stability, especially against exonuclease degradation, and a decrease in the formation of the initiation complex of mRNAs for protein synthesis. Certain prokaryotic mRNAs containing a 5' terminal cap structure are translated as efficiently as or more efficiently than eukaryotic mRNAs in a eukaryotic cell-free protein synthesizing system. Also a cap requirement has been observed for splicing eukaryotic substrate RNAs. A method using E. coli RNA Polymerase primed with m7G(5' )ppp(5' )G or m7G(5' )ppp(5' )A for an efficient in vitro synthesis of capped RNAs has been developed by Contreas. Larger amounts of capped RNAs are produced by transcription systems using SP6 RNA polymerase primed with m7G(5' )ppp(5' )G.
Biochain Institute Inc Total RNA - Human Adult Normal Tissue: Gallbladder, 10 ug/PK
BioChain's Total RNAs are isolated from a wide variety of documented human normal, diseased, and tumor tissues, mouse, rat, monkey, and plant tissues. Total RNA isolation is performed using proprietary techniques. Contamination by RNase, genomic DNA polysaccharides, and proteoglycans has been effectively eliminated. The integrity of the total RNAs is assured by checking for a ratio of greater than 1:1 between 28s and 18s ribosomal RNA. High efficiency reverse transcription using the Total RNA is demonstrated.
Biochain Institute Inc Total RNA - Human Adult Normal Tissue: Heart, 50 ug/PK
BioChain's Total RNAs are isolated from a wide variety of documented human normal, diseased, and tumor tissues, mouse, rat, monkey, and plant tissues. Total RNA isolation is performed using proprietary techniques. Contamination by RNase, genomic DNA polysaccharides, and proteoglycans has been effectively eliminated. The integrity of the total RNAs is assured by checking for a ratio of greater than 1:1 between 28s and 18s ribosomal RNA. High efficiency reverse transcription using the Total RNA is demonstrated.
Biochain Institute Inc Total RNA - Human Adult Normal Tissue: Trachea, 50 ug/PK
BioChain's Total RNAs are isolated from a wide variety of documented human normal, diseased, and tumor tissues, mouse, rat, monkey, and plant tissues. Total RNA isolation is performed using proprietary techniques. Contamination by RNase, genomic DNA polysaccharides, and proteoglycans has been effectively eliminated. The integrity of the total RNAs is assured by checking for a ratio of greater than 1:1 between 28s and 18s ribosomal RNA. High efficiency reverse transcription using the Total RNA is demonstrated.