Market Scenario:. The global market of oligonucleotide synthesis is growing at a rapid pace. The global oligonucleotide synthesis market is growing at the CAGR of around 10.3% for the forecasted period. The major factors that are influencing the market for oligonucleotide synthesis are increasing advancement in field of healthcare, increasing demand for innovation in the field of life science and medical academics, increasing investment by the government for the development of genomic technologies, increasing demand for oligonucleotide synthesis technologies by the public and private research firms. Furthermore increasing application of oligonucleotide synthesis in diagnostic, genetic testing, research, therapeutics, gene synthesis, library preparation, drug target screening, and others is further influencing the growth of the oligonucleotide synthesis market globally.. Key Players for Oligonucleotide Synthesis Market:. Integrated DNA Technologies, Inc (U.S), GE Healthcare (U.S.), Agilent ...
Oligonucleotides are short nucleic acid polymers used in research, genetic testing and forensics. Oligonucleotides are usually made up of 13 to 25 nucleotides and are designed to hybridize specifically to DNA or RNA sequences. Solid-phase clinical synthesis is used to manufacture these small bits of nucleic acid for use in polymerase chain reaction (PCR), DNA sequencing, library construction and artificial gene synthesis.. Oligonucleotide synthesis is the chemical synthesis of relatively short fragments of nucleic acids with defined chemical structure/sequence.In the enzymatic process of DNA synthesis, deoxy-ribonucleotide-5-tri-phosphates are used as substrates during polymerization. In addition, this process requires a primer and a template.. Full Research Report On Global Oligonucleotide Synthesis Market Analysis available @ https://www.millioninsights.com/industry-reports/oligonucleotide-synthesis-market. The most frequently used oligonucleotide synthesis strategy is based upon ...
Oligonucleotides are short nucleic acid polymers used in research, genetic testing and forensics. Oligonucleotides are usually made up of 13 to 25 nucleotides and are designed to hybridize specifically to DNA or RNA sequences. Solid-phase clinical synthesis is used to manufacture these small bits of nucleic acid for use in polymerase chain reaction (PCR), DNA sequencing, library construction and artificial gene synthesis.. Oligonucleotide synthesis is the chemical synthesis of relatively short fragments of nucleic acids with defined chemical structure/sequence.In the enzymatic process of DNA synthesis, deoxy-ribonucleotide-5-tri-phosphates are used as substrates during polymerization. In addition, this process requires a primer and a template.. Full Research Report On Global Oligonucleotide Synthesis Market Analysis available @ https://www.millioninsights.com/industry-reports/oligonucleotide-synthesis-market. The most frequently used oligonucleotide synthesis strategy is based upon ...
According to the new market research report The Report "Oligonucleotide Synthesis Market by Product & Services (Equipment, Reagent, Primer, Probe, Custom Oligos), End-User (Research, Pharmaceutical & Biotechnology), Application (Diagnostics, PCR, QPCR, Gene Synthesis, NGS, DNA, RNAi) - Global Forecast to 2019" provides a detailed overview of the major drivers, restraints, challenges, opportunities, current market trends, and strategies impacting the oligonucleotide synthesis market along with the estimates and forecasts of the revenue and competitive analysis.. This report studies the oligonucleotide synthesis market by products and services, applications, end users, and geography.. Oligonucleotide synthesis has a vast number of applications in nucleic acid array-based technologies, library preparations, next-generation sequencing methods, genomics, nucleic acid-based detection, cell cultures, diagnostics, therapeutics, human identity testing, cloning and genetic engineering, and synthetic ...
Sales, means the sales volume of Oligonucleotide Synthesis Revenue, means the sales value of Oligonucleotide Synthesis This report studies Oligonucleotide Synthesis in China market, focuses on the top players in China market, with capacity, production, price, revenue and market share for each manufacturer, covering Agilent Technologies Biosearch Technologies, Inc Eurofins Genomics
TY - JOUR. T1 - Receptor-mediated hepatic uptake of M6P-BSA-conjugated triplex-forming oligonucleotides in rats. AU - Ye, Zhaoyang. AU - Cheng, Kun. AU - Guntaka, Ramareddy V.. AU - Mahato, Ram I.. PY - 2006/5/1. Y1 - 2006/5/1. N2 - Excessive production of extracellular matrix, predominantly type I collagen, results in liver fibrosis. Earlier we synthesized mannose 6-phosphate-bovine serum albumin (M6P-BSA) and conjugated to the type I collagen specific triplex-forming oligonucleotide (TFO) for its enhanced delivery to hepatic stellate cells (HSCs), which is the principal liver fibrogenic cell. In this report, we demonstrate a time-dependent cellular uptake of M6P-BSA- 33P-TFO by HSC-T6 cells. Both cellular uptake and nuclear deposition of MoP-BSA-33P-TFO were significantly higher than those of 33P-TFO, leading to enhanced inhibition of type I collagen transcription. Following systemic administration into rats, hepatic accumulation of MoP-BSA-33P-TFO increased from 55% to 68% with the number of ...
Transfection of cells with gene-specific, single-stranded oligonucleotides can induce the targeted exchange of one or two nucleotides in the targeted gene. To characterize the features of the DNA-repair mechanisms involved, we examined the maximal distance for the simultaneous exchange of two nucleotides by a single-stranded oligonucleotide. The chosen experimental system was the correction of a hprt- point mutation in a hamster cell line, the generation of an additional nucleotide exchange at a variable distance from the first exchange position and the investigation of the rate of simultaneous nucleotide exchanges. The smaller the distance between the two exchange positions, the higher was the probability of a simultaneous exchange. The detected simultaneous nucleotide exchanges were found to cluster in a region of about fourteen nucleotides upstream and downstream from the first exchange position. We suggest that the mechanism involved in the repair of the targeted DNA strand utilizes only a short
Cumulative evidence supports a role for aberrant Stat3 activation in transformation and tumor progression. We previously demonstrated increased Stat3 activation in head and neck carcinogenesis, where Stat3 contributes to the loss of growth control by an antiapoptotic mechanism (5). Targeting Stat3 with antisense oligonucleotides or dominant-negative mutants resulted in apoptosis and modulation of Stat3 regulated genes in several cancer-derived cell lines including multiple myeloma, melanoma, mycosis fungoides, and SCCHN (5, 38-40). The present study provides evidence that Stat3 activation can be targeted as an antitumor strategy. We used a novel decoy oligonucleotide approach to show selective abrogation of activated Stat3 accompanied by inhibition of tumor cell growth and abrogation of Stat3-mediated target gene expression. The lack of inhibitory effects on normal oral keratinocytes suggests that a Stat3 decoy strategy may selectively block the growth of cancer cells with relatively little ...
... , End Users, Region/Country Data (17 Region/Countries), and Competitive Landscape - Analysis and Forecast, 2019-2029. Key questions answered in this report: How much revenue was generated by the global oligonucleotide synthesis market in 2018 and how is it expected to perfor
Oligonucleotides can be used to site specifically substitute a single nucleotide of transfected target genes in both Anopheles...
Arrayit Oligonucleotide Microarray modified primer and two-color fluorescent probe oligonucleotide synthesis including 200 nmole synthesis scale sufficient to genotype 10,000 samples and quality control by mass spectroscopy. Each synthesis includes two primers and two probes (4 oligonucleotides total). Quantity pricing is available for large projects.
Oligonucleotides are short sequences of nucleotides (RNA or DNA), typically with twenty or fewer bases. Automated synthesizers allow the synthesis of oligonucleotides up to 160 to 200 bases. The length of a synthesized base is usually denoted by mer (from Greek meros "part"). For example, a fragment of 25 bases would be called a 25-mer. Oligonucleotides are often used as probes for detecting complementary DNA or RNA because they bind readily to their complements. Examples of procedures that use oligonucleotides are DNA microarrays, Southern blots, fluorescent in situ hybridization (FISH), and the synthesis of artificial genes. Oligonucleotides composed of DNA (deoxyoligonucleotides) are often used in the polymerase chain reaction (PCR), a procedure that can be employed to amplify almost any piece of DNA. In this instance, the oligonucleotide is often referred to as a primer, or a short piece of DNA that binds to its complementary target sequence. This generates a place for a polymerase to ...
Geometric Approaches to Gibbs Energy Landscapes and DNA Oligonucleotide Design: 10.4018/ijnmc.2011070104: DNA codeword design has been a fundamental problem since the early days of DNA computing. The problem calls for finding large sets of single DNA strands that
Small interfering (si) RNAs and antisense oligonucleotides (ASOs; here for simplicity reasons, both referred to as oligonucleotides) are small synthetic RNA or DNA molecules with a sequence complementary to a (pre)mRNA. Although the basic mechanisms of action between siRNAs and ASO are distinct, a sequence-specific interaction of the both oligonucleotides with the target (pre)mRNA alters the targets fate, which includes highly effective sequence-specific blockade of translation and consequently depletion of the corresponding protein. For a number of years, these oligonucleotides have been used as a tool in biological research to study gene function in vitro. More recently, safe and specific delivery of these oligonucleotides to the liver of mammals has been achieved and optimized. This not only allowed their use for in vivo gene studies in physiology and disease, but also opened the opportunity for the development of a new generation of RNA-specific drugs for therapeutic purposes. In 2013, the ...
Oligonucleotide synthesis market segmented global market by product(Synthesized Oligonucleotides, Custom Oligonucleotides), application(Research, Therapeutics, Diagnostics), end users & region.
The present invention relates to a method for detecting gene polymorphism by PCR, using, as a primer, an oligonucleotide, wherein the third nucleotide from the 3′-end thereof is a 2′-O,4′-C-ethylene nucleotide (ENA) unit, the other oligonucleotides are natural oligonucleotides, the 3′-end position thereof is a nucleotide complementary to the nucleotide of the reference sequence of a polymorphic sequence of a target gene, and the other positions are nucleotides complementary to the nucleotide sequence of the target gene, or an oligonucleotide, wherein the 3′-end of the nucleotide sequence thereof is a polymorphic position, the second nucleotide from the 3′-end thereof is a nucleotide having a base that is not complementary to a gene to be detected, and the third nucleotide from the 3′-end thereof is a 2′-O,4′-C-ethylene nucleotide (ENA) unit; oligonucleotides used in detection of gene polymorphism; and a kit for detecting gene polymorphism, comprising the above oligonucleotides.
From BioPortfolio: The global oligonucleotide synthesis market is expected to reach $1,712.1 million by 2019 from $1,070.7 million in 2014, growing at a CAGR of 9.8% from 2014 to ...
Oligonucleotide Synthesis Market by Product & Services (Primer, Probe, Custom, Predesigned, Reagent Equipment), Application (Research, PCR, Gene, DNA, NGS, Diagnostic, RNAI), End user (Academic, Pharmaceutical, - Market research report and industry analysis - 10520121
Oligonucleotide Synthesis Market Size, Share & Trends Analysis Report By End Use, By Product (Column-based, Array-based, Services), By Application (PCR Primer, FISH), And Segment Forecasts, - Market research report and industry analysis - 12015003
This invention relates to a support for oligonucleotide synthesis and more particularly to a necleoside-linker/polymer support composite having the general formula P--S wherein P is a polymer support which bears oxirane, aziridine or episulfide groups or which contains good leaving groups for nucleophilic displacement; and S is a nucleoside-linker having the general formula W--(CH.sub.2).sub.a --X--(CH.sub.2).sub.b --Y--(CH.sub.2).sub.c --Z wherein W and Z each independently comprise a nucleophile; X and Y which, independently may or may not be present, comprise groups of high hydrophilicity; and a, b, c are integers from 0 to 9, wherein a plus b plus c exceeds 6.
Oligonucleotide Synthesis Market by Product & Services (Primer, Probe, Custom, Predesigned, Reagent Equipment), Application (Research, PCR, Gene, DNA, NGS,...
Find all books from Piet Herdewijn (Editor) - Oligonucleotide Synthesis: Methods and Applications. At find-more-books.com you can find used, antique and new books, COMPARE results and immediately PURCHASE your selection at the best price. 1617374415
Asia Pacific Oligonucleotide Synthesis Market expected to reach US$ 872.98 Mn in 2027 from US$ 334.26 Mn in 2018 the market is estimated to grow with a CAGR of 14.7% from 2019-2027 and segmented into Product, Application and End User.
The efficient incorporation of reporter groups into oligonucleotides at specific sites has been facilitated by the synthesis of a novel modified thymidine monomer with an FMOC-protected hydroxyl group on a linker. The primary hydroxyl group can be deprotected during or after solid-phase oligonucleotide synthesis and reacted with any reporter phosphoramidite.. Full text not available from this repository.. ...
The present invention is directed to methods and materials for RNA-mediated gene assembly from oligonucleotide sequences. In some embodiments, the oligonucleotides used for gene assembly are provided in an array format. An RNA polymerase promoter is appended to surface-bound oligonucleotides and a plurality of RNA copies of each oligonucleotide are then produced with an RNA polymerase. These RNA molecules self-assemble into a desired full-length RNA transcript by hybridization and ligation. The resulting RNA transcript may then be converted into double strand DNA useful in a variety of applications including protein expression.
Methods for preparing oligonucleotide analogs which have improved nuclease resistance and improved cellular uptake are provided. In preferred embodiments, the methods involve reductive coupling of 3-
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Descriptive info: Homepage.. Welcome to BioSpring.. BioSpring , The Oligo Company.. Expertise in oligonucleotide synthesis.. Flexibility by open source oligonucleotide production system.. Synthesis of oligonucleotides.. Standard analyses of oligonucleotides.. Additional analyses of oligonucleotides.. Superstructures: Biological significance and structure.. siRNA, RNAi.. Interfering RNA.. Hybridisation of siRNA molecules.. Quality and delivery time.. Phosphonoacetates.. Antisense molecules.. RNase H activity.. Transport into the cells.. Advantages of phosphonoacetates.. Scales and Modifications.. Unmodified oligonucleotides.. Phosphorothioates.. RNA.. Modified RNA.. Methylphosphonates.. Phosphonoacetate oligonucleotides (PACE).. RNAi, siRNA miRNA.. 5 modifications.. 3 modifications.. Internal modifications.. Dual labeled probes.. Additional services.. Delivery.. Qualification and validation.. BioSpring GMP Manufacturing movie.. Oligonucleotides for diagnostic applications.. Certificate ISO ...
Oligonucleotides are single-stranded and short RNA or DNA molecule that have a wide range of applications in research forensics and genetic testing. Oligon
Because oligonucleotides are short sequences of nucleic acid bases, their association in solution with complementary strands (hybridization) is often seen to conform to a simple two-state model. However, experimental evidence suggests that, despite their short length, oligonucleotides may hybridize through multiple states involving intermediates. We investigate whether these apparently contradictory scenarios are possible by imposing different levels of sequence specificity on a lattice model of oligonucleotides in solution, which we introduced in Part I [J. C. Araque et al., J. Chem. Phys. 134, 165103 (2011)]. We find that both multiple-intermediate (weakly cooperative) and two-state (strongly cooperative) transitions are possible and that these are directly linked to the level of sequence specificity. Sequences with low specificity hybridize (base-by-base) by way of multiple stable intermediates with increasing number of paired bases. Such intermediate states are weakly cooperative because the ...
The over-expression of human mdr1 (multidrug resistant) gene leads to intensive efflux of cytotoxic anticancer drugs out of malignant cells and aggressive tumor behavior. Rational mdr1 gene targeting by TFO-s within the promoter region represents a perspe
Applications requiring long oligonucleotides (,50 bases) e.g., microarray applications, cloning and/or gene synthesis, have increased the need for instrumentation that can accurately characterize these molecules. The method of choice for these oligonucleotides is ESI-MS. The target molecules are ionized into multiple charge states producing a waveform that can be de-convoluted into parent peaks. As only the charge state will vary for the ions, oligonucleotides with high molecular weights can be analyzed using this method. Additionally, the inherently milder ionization conditions make this analytical technique a great tool for the analysis of labile compounds such as common quenchers, e.g., dabcyl, BHQs, used in dual-labeled fluorogenic probes. The ESI-MS systems have mass resolution of approximately 0.03%, i.e., resolution of +/- 3 Da on a 10 kDa oligonucleotide.. ...
2′-O-modified ribosyl nucleosides and modified oligonucleotides containing such nucleotides are disclosed. Oligonucleotides are disclosed that have increased binding affinity as shown by molecular modeling experiments. The 2′-O-modified nucleosides of the invention include ring structures that position the sugar moiety of the nucleosides preferentially in 3′ endo geometries.
Despite the many methodological options available for mutation detection, the choice is limited, by the necessity to ensure the highest sensitivity of detection for all types of changes while keeping costs and time of analysis within a reasonable limit. The present study extends to large and complex genes, like BRCA1, the applications of the FAMA method using large PCR amplicons (up to 1.4 kb). A key feature of this diagnostic strategy is the robust and economical two-step procedure for strand-specific labeling of PCR products using chimeric oligonucleotides and universal fluorescent primers (Fig. 1)⇓ . This labeling method is cost-effective, because it requires only one set of universal fluorescent primers, and allows reproducible amplification of all exons and splice sites of BRCA1 using homogeneous PCR conditions.. In the blind-test screening for changes in exon 11 (Table 2)⇓ different kinds of mutations and polymorphisms (various microdeletions/insertions involving 1 to 11 nucleotides as ...
A theory and graphical presentation for the analysis of helix structure and deformations in oligonucleotides is presented. The parameters "persistence" and "flexibility" as defined in the configurational statistics of polymers of infinite length are reformulated at the oligonucleotide level in an extension of J. A. Schellmans method [(1974) Biopolymers, Vol. 17, pp. 217-226], and used as a basis for a systematic "Persistence Analysis" of the helix deformation properties for all possible subsequences in the structure. The basis for the analysis is a set of link vectors referenced to individual base pairs, and is limited to sequences exhibiting only perturbed rod-like behavior, i.e., below the threshold for supercoiling. The present application of the method is concerned with a physical model for the angular component of bending, so the link vectors are defined as the unit components of a global helix axis obtained by the procedure "Curves" of R. Lavery and H. Sklenar [(1988) J. Biomol. Struct. ...
Methods and Results: Microarray analysis revealed subsets of miRNAs that were upregulated or downregulated in cardiac ventricles from mice at 1 and 10 days of age (P1 and P10). Interestingly, miR-195 (a member of the miR-15 family) was the most highly upregulated miRNA during this period, with expression levels almost 6-fold higher in P10 ventricles relative to P1. Precocious overexpression of miR-195 in the embryonic heart was associated with ventricular hypoplasia and ventricular septal defects in β-myosin heavy chain-miR-195 transgenic mice. Using global gene profiling and argonaute-2 immunoprecipitation approaches, we showed that miR-195 regulates the expression of a number of cell cycle genes, including checkpoint kinase 1 (Chek1), which we identified as a highly conserved direct target of miR-195. Finally, we demonstrated that knockdown of the miR-15 family in neonatal mice with locked nucleic acid-modified anti-miRNAs was associated with an increased number of mitotic cardiomyocytes and ...
LONDON - In the past year, the value of the worlds oligonucleotide pool exceeded USD 1.29 billion. It is expected to go beyond USD 2.32 billion, registering an 8.5% CAGR over 2017-2022. Robust growth is attributed to such factors as increasing Big PharmaCos investments in oligonucleotide drug development, constantly widening application area of oligonucleotides and also rising involvement of CMOs in therapeutic oligonucleotides manufacturing, amid others.. Still, there are certain barriers to the further growth in the oligonucleotide pool market, for instance, inaccuracy issues associated with specific oligonucleotides and complexity in the manufacturing technology.. At present, North America captures the major share of the global oligonucleotide pool market; as of 2016, the regions share was slightly over 42%.. Some of the prominent global market players include Creative Biogene, CustomArray, Agilent Technologies, TriLink BioTechnologies, MYcroarray, Integrated DNA Technologies, Twist ...
User:Gabriel Wu,Gabriel Wu]] 00:58, 9 February 2013 (EST): From people who do this kind of work, they tell me that assembling a 3 Kb plasmid takes about 3 full days of lab work. The cost of Gibson master mix from NEB is $154.00 for 10 reactions ($15 for one reaction). The cost of Phusion master mix is $170 for 100 reactions ($8 for 4 PCR reactions). Plates, media, and competent cells add a marginal cost (I would estimate generously no more than $20). Finally, oligoucleotides are about $15 a piece. This assembly would probably take about 8 long oligonucleotides ($160). Then finally, think about how much you make and add your 3 day cost. I estimate generously at about $300 for three days work. Add it all up, you get about $503. A two-fold difference at I think reasonably generous estimates. It becomes a question if whether your time is beter spent in other places and how quickly do you need the part ...
Gabriel Wu 00:58, 9 February 2013 (EST): From people who do this kind of work, they tell me that assembling a 3 Kb plasmid takes about 3 full days of lab work. The cost of Gibson master mix from NEB is $154.00 for 10 reactions ($15 for one reaction). The cost of Phusion master mix is $170 for 100 reactions ($8 for 4 PCR reactions). Plates, media, and competent cells add a marginal cost (I would estimate generously no more than $20). Finally, oligoucleotides are about $15 a piece. This assembly would probably take about 8 long oligonucleotides ($160). Then finally, think about how much you make and add your 3 day cost. I estimate generously at about $300 for three days work. Add it all up, you get about $503. A two-fold difference at I think reasonably generous estimates. It becomes a question if whether your time is beter spent in other places and how quickly do you need the part ...
Inhibitors of STAT signaling have become increasingly important because of the role of STATs in the pathogenesis of human diseases (15, 18, 44, 45). While significant progress has been made in using antisense or decoy oligonucleotides (46) and dominant-negative mutants (27, 38, 42, 47) to elucidate STAT signaling and biological effects, these STAT inhibitory modalities do not easily lend themselves to clinical applications. Another approach has been to use small-molecule inhibitors of the upstream tyrosine kinases that phosphorylate and activate STATs (15, 36, 48). However, because other signaling pathways are also activated downstream of tyrosine kinases, non-Stat3-related biological effects might ensue from inhibition of these kinases. In an effort to develop Stat3-specific small-molecule inhibitors, we previously showed that a Stat3 SH2 domain-binding phosphopeptide, PY*LKTK, and its truncated tripeptide derivatives, PY*L and AY*L, disrupt Stat3 activity (21), thus providing leads for ...
Fast and reliable custom oligonucleotide synthesis service at competitive price. Bioneer is one of the worlds largest suppliers of synthetic oligonucleotides. Every Bioneer oligo is purified free-of-charge utilizing our unique Bio-RP cartridge purification technology and quality checked by MALDI-TOF.
We signed the Oligonucleotides Therapeutics Discovery Collaboration Agreement with Nissan Chemical Co., Ltd.. We aim to create new oligonucleotide therapeutics based on a new oligonucleotide therapeutics structure by combining the two companies oligonucleotide therapeutics drug discovery platform technologies.. Please click here for details.. ...
All current genetic testing methods require synthetic oligonucleotide primers and probes. At ATDBio we make high quality custom qPCR and LAMP primers and probes, working with our customers to help them develop simpler, faster and more accurate diagnostic methods. Were using our specialist nucleic acid expertise to accelerate the global response to the pandemic, helping to get the world back up and running quickly and safely. Weve already made oligos for millions of tests, and were scaling up even further. ...
Oligonucleotide synthesis is essentially the synthesis of nucleic acid fragments that results in defined chemical structures with purities of different sizes. When you´re looking for the most effective modified product for your oligo synthesis, you´re going to want to narrow down the companies that you´re going to work with by high quality services that they offer. Here are some key components that you´re going to want to keep in mind when shopping around.. Quality. Quality is obviously the main concern that you´re going to have because the only way that you can validate what they claim is through user reviews or testimonials. You´re not going to have a physical sample that you get to take an in-depth look at, rather an assortment of pictures put together by the company.. Be sure that the company is specific in their details to ensure that you get exactly what you want. For example, if they´re offering single stranded or double-stranded DNA, be sure that they give you the exact number of ...
Oligonucleotides having approximately 8 to 18 nucleotide units and a 3-tail which includes asteroid structure attached to the 3-end through the A ring of the steroid skeleton and which form substantially stable duplexes at physiological temperature, have selective cytotoxic activity against certain tumor cell lines.
AccuPrep® PCR Purification Kit is designed for the purification of up to 10 ug of DNA fragment from PCR and other enzymatic products within 5 minutes. The size range for effective purification is 100 bp ~10 kb, thus common 20 ~ 40 mer oligonucleotides are removed. The recovery yield exceeds 70~90%. Elution volume can be as little as 30 uL when concentrated product is needed ...
Author: Baumann, U.; Genre: Journal Article; Published in Print: 1986-09; Title: A Specific binding of hairpin oligonucleotides to homo-oligonucleotides by triplet recognition.
Reading Oligonucleotides Information - posted in General Lab Techniques: Good evening. I need a help to read the information on the primer information sheet. What is the different between Tm(1M Na+) and Tm(50mM Na+)?
TAG Copenhagen is a leading manufacturer of oligonucleotides and a distributor of life science products across Europe and other parts of the world...
Berry & Associates Inc. offers nucleosides, fluorescent markers, and other tools for biomedical research. Berry also manufactures nucleoside phosphoramidites, available through Glen Research Corporation, for oligonucleotide synthesis.