Idtdna

PrimeTime qPCR Probe Assays consist of a primer pair and fluorescently labeled 5′ nuclease probe. Obtain predesigned sequences for human, mouse, or rat for easy selection based on multiple criteria such as exon location and number of transcripts. Create custom assays for any sequence from any species using the …

Idtdna. Our Scientific Applications Support team has assembled a list of frequently asked questions to help you find answers quickly. Filter using one or more categories to focus on specific topics, or use the search bar to perform a text search.

Email: [email protected]. Phone: +65 6775 9187. Australia. Email: [email protected]. Phone: 1800 845 181. All contact information. Additional resources: Frequently asked questions (FAQs) How long is my data retained in the rhAmpSeq CRISPR Analysis Tool?

The IDT xGen hybridization capture products includes a variety of predesigned panels and custom panels available in a range of panel sizes. An updated, automation-friendly protocol is available for high-throughput applications. The xGen Hyb Panel Design Tool can help guide you through the process of designing a panel specific for your research. The curves represent the theoretical yield for different lengths of oligos based on a coupling efficiency of 99.4% (IDT Oligos, n = 126) and 99.1% (other suppliers, n = 134 from three different suppliers) using the formula: percent full length product = (eff ) (n-1)*100 where eff = coupling efficiency (for example, 99.4% = 0.994) and (n–1) …Overview. Use of the CRISPR (clustered regularly interspaced short palindromic repeats) and associated Cas9 enzyme for genome editing has been a major technological breakthrough, making genome modification in cells or organisms faster, more efficient, and more robust than previous genome editing methods. The Alt-R …© 2024 Integrated DNA Technologies, Inc. Trademarks contained herein are the property of Integrated DNA Technologies, Inc. or their respective owners, and may be ...IDT offers a range of products and services for DNA sequencing, from whole genome to targeted sequencing, using next generation sequencing (NGS) technology. Learn about …Figure 3. IDT gBlocks and gBlocks HiFi Gene Fragments produce a higher percentage of correct colonies when compared to two other suppliers. Based on screening and sequencing of 24 colonies per sequence, IDT’s fragments were the only fragments to have greater than 75% correct colonies with the desired full …Pros. Fast, flexible design – Essentially, CRISPR-Cas9 gene editing requires 2 components: the Cas nuclease and a guide RNA. In some cases, researchers opt to use the 2-part crRNA-tracrRNA system while in others they use an sgRNA. Once the guide RNA and endonuclease bind to each other they form a …

Researchers performing qPCR will often create a standard curve based on nanograms of amplicon, and then need to convert the resulting nanograms detected to copy number. The formula for making this conversion is: Figure 1. Where: X = amount of amplicon (ng) N = length of dsDNA amplicon. 660 g/mol = average …Ideal conditions for standard DNA oligonucleotides. IDT has tested the stability of oligonucleotides following various storage conditions. The results of these studies indicate that the most stable temperature at which to store a standard DNA oligonucleotide is –20°C. An oligo stored at –20°C is stable for at least 24 months …Our Scientific Applications Support team has assembled a list of frequently asked questions to help you find answers quickly. Filter using one or more categories to focus on specific topics, or use the search bar to perform a text search.Demaris has spent her career in the Life Sciences and Diagnostics space, and has been with Danaher since 2009. She joined IDT as President in July 2021 from Phenomenex, where she also served as President. Prior to Phenomenex, Demaris served in several senior leadership positions at Beckman Coulter Life Sciences, …IDT DNA is a leading provider of biotechnology products and services. To access its online ordering tools, you need to sign in or create a free [email protected] +65 6775 9187: Australia: [email protected]: 1800 845 181: Canada: [email protected]: 1 800 328 2661: China: [email protected]: 400 668 3770: Europe: emea …

Product details. Megamer ssDNA Fragments are single-stranded genomic blocks for research applications such as homology-directed repair of CRISPR-mediated genome editing , in vitro transcription, and more. Megamer fragments are 201–2000 bases in length and are generated from clonally derived DNA. Megamer ssDNA …Jun 15, 2012 · Figure 1. Select the OligoAnalyzer Tool from the TOOLS menu on any IDT webpage. The OligoAnalyzer Tool link is found under the Oligo Design & Handling section. Enter your sequence into the “Sequence” box in the 5’ to 3’ orientation (Figure 2, arrow A). The OligoAnalyzer Tool accommodates DNA, RNA, mixed bases, and a variety of ... Please sign in to use IDT’s custom online ordering tools. If you don’t yet have an IDT account, join the IDT community! Create your free account today and enjoy unlimited access to our innovative web tools, streamlined ordering, and expert educational content. Trademarks contained herein are the property of Integrated DNA …Figure 3. IDT gBlocks and gBlocks HiFi Gene Fragments produce a higher percentage of correct colonies when compared to two other suppliers. Based on screening and sequencing of 24 colonies per sequence, IDT’s fragments were the only fragments to have greater than 75% correct colonies with the desired full …The Codon Optimization Tool converts the DNA, or protein sequence, from one organism for expression to another. The IDT algorithm provides the best sequence option by screening and filtering sequences to lower complexity and minimize secondary structures. Rebalance codon usage. Decrease sequence complexity. …

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OligoAnalyzer™ Tool. Understand the expected behavior of your oligos before you order them. Quickly see GC content, melting temperature, and more. Identify secondary structure potential. Minimize dimerization. Use NCBI Blast. Gene knockdown is a major approach which has long been used in cell and molecular biology research to determine the function or role of a given gene. In addition to basic research on gene function, gene knockdown is also used therapeutically. Two examples of gene knockdown-based therapeutics in current …AIT is Austria’s largest applied non-university research institute. AIT’s Molecular Diagnostics unit focuses on non- and minimally invasive methods to provide contract research services for transcriptomics, epigenetics, and immunomics-type projects. Their research expertise ranges from biomarker discovery to assay design and …PrimeTime qPCR Probe Assays consist of a primer pair and fluorescently labeled 5′ nuclease probe. Obtain predesigned sequences for human, mouse, or rat for easy selection based on multiple criteria such as exon location and number of transcripts. Create custom assays for any sequence from any species using the …Illumina sequencing by synthesis is a common approach to NGS that relies on the generation of DNA strand “clusters”─multiple copies of the same DNA fragment bound to a solid surface called a flow cell. These clusters are synthesized by a process called “bridge amplification” ─ a PCR reaction on a chip where …

qPCR & PCR. PrimeTime One-Step 4X Broad-Range Master Mix Protocol (522 KB) PrimeTime One-Step RT-qPCR Master Mix protocol (394 KB) rhAmp SNP Genotyping (472 KB) RNase H2–Dependent PCR (rhPCR) protocol (628 KB) qPCR Dye calibration on AB systems protocol (609 KB) PrimeTime qPCR Assay Plate resuspension protocol (183 KB) A complete listing of IDT products available for ordering. For research use only. Not for use in diagnostic procedures. Unless otherwise agreed to in writing, IDT does not intend for these products to be used in clinical applications and does not warrant their fitness or suitability for any clinical diagnostic use. Prove it. We'll help. Our custom oligo synthesis platforms provide innovative research tools for genomics applications using NGS, CRISPR, qPCR, and synthetic biologyRNA oligos are short, single- or double-stranded synthetic RNA sequences that can be used in nearly any RNA­ specific molecular biology application. Using the Oligo Entry ordering tool, you can design your sequences to contain unmodified RNA bases, 2'-O-methyl RNA bases, or chimeric DNA bases. You can select from …Product details. Megamer ssDNA Fragments are single-stranded genomic blocks for research applications such as homology-directed repair of CRISPR-mediated genome editing , in vitro transcription, and more. Megamer fragments are 201–2000 bases in length and are generated from clonally derived DNA. Megamer ssDNA …IDT offers a range of qPCR products to quantify mRNA levels, including PrimeTime probes, master mixes, and primer assays. Learn more about the features, benefits, and …The PAM site must be present immediately downstream of the protospacer element for cleavage to occur. Research by IDT scientists has shown that the Alt-R CRISPR-Cas9 System provides the highest percentage of on-target genome editing when compared to competing designs of native S. pyogenes …IDT offers a range of products and services for DNA sequencing, from whole genome to targeted sequencing, using next generation sequencing (NGS) technology. Learn about …

Jun 15, 2012 · Figure 1. Select the OligoAnalyzer Tool from the TOOLS menu on any IDT webpage. The OligoAnalyzer Tool link is found under the Oligo Design & Handling section. Enter your sequence into the “Sequence” box in the 5’ to 3’ orientation (Figure 2, arrow A). The OligoAnalyzer Tool accommodates DNA, RNA, mixed bases, and a variety of ...

Illumina sequencing by synthesis is a common approach to NGS that relies on the generation of DNA strand “clusters”─multiple copies of the same DNA fragment bound to a solid surface called a flow cell. These clusters are synthesized by a process called “bridge amplification” ─ a PCR reaction on a chip where …Jun 15, 2012 · Figure 1. Select the OligoAnalyzer Tool from the TOOLS menu on any IDT webpage. The OligoAnalyzer Tool link is found under the Oligo Design & Handling section. Enter your sequence into the “Sequence” box in the 5’ to 3’ orientation (Figure 2, arrow A). The OligoAnalyzer Tool accommodates DNA, RNA, mixed bases, and a variety of ... For long oligos, IDT offers an enriched synthesis cycling and proprietary solid support that has an even higher coupling efficiency of 99.6% (Figure 4). IDT Ultramer™ DNA Oligos are suggested for any customer requiring oligos between 45 and 200 bases in length. Heterodimer analysis works the same way as self-dimer analysis. Use the 'Hetero-Dimer' button in the OligoAnalyzer program to check for primer dimers. Enter the sequence of your forward primer into the sequence box, and then click 'Hetero-Dimer.'. This will open a second box below the original sequence box, in which you enter the sequence of ... OligoAnalyzer is a primer analysis tool for oligonucleotides. Design and analyze DNA and RNA oligos for insight into behavior and properties. Jun 15, 2012 · Figure 1. Select the OligoAnalyzer Tool from the TOOLS menu on any IDT webpage. The OligoAnalyzer Tool link is found under the Oligo Design & Handling section. Enter your sequence into the “Sequence” box in the 5’ to 3’ orientation (Figure 2, arrow A). The OligoAnalyzer Tool accommodates DNA, RNA, mixed bases, and a variety of ... The PrimerQuest Tool offers 4 design options that are based on algorithms specific for common experimental setups (Figure 1). By default, your results return the 5 best primer or assay designs. PCR (2 primers) qPCR (2 primers + probe; for use in 5′ nuclease assays) qPCR (2 primers; for use with intercalating … The IDT Community Blog. Both arrayed and pooled CRISPR screens can identify important genes or genetic sequences within a genome. We contrast using pooled versus arrayed CRISPR guide RNA libraries to perform functional genomics screens. While pooled libraries can have cost benefits, arrayed libraries can often provide greater accuracy.

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qPCR & PCR. PrimeTime One-Step 4X Broad-Range Master Mix Protocol (522 KB) PrimeTime One-Step RT-qPCR Master Mix protocol (394 KB) rhAmp SNP Genotyping (472 KB) RNase H2–Dependent PCR (rhPCR) protocol (628 KB) qPCR Dye calibration on AB systems protocol (609 KB) PrimeTime qPCR Assay Plate resuspension protocol (183 KB) DNA oligos. First-time purchase of 25nm DNA oligos, limited to quantities 4-10. Expires: April 30, 2024. Promo code: 25nm-50. Order Today. Custom primers. Primer design is key for generating high-quality PCR results. IDT offers a variety of custom primers and easy-to-use primer design tools to help ensure that you generate the primers you need to drive your research forward. qPCR solutions. Overview. Simplify and optimize your next generation sequencing of DNA, RNA, and ctDNA with IDT’s full spectrum of solutions for your lab’s needs. With reliable individual components, create a flexible workflow to streamline your sequencing process using xGen™ NGS. For full assay solutions including data analysis, discover or design … Genes and MiniGene™ Synthetic Genes are NGS-verified, circular double-stranded DNA in a plasmid. DNA sequences 25 bp to 5 kb are provided with IDT’s in-house cloning vectors, or a custom plasmid vector of your choice (see Table 1) without additional cloning fees. Sequences greater than 5 kb can be reviewed for acceptance as a custom project. IDT offers a range of qPCR products to quantify mRNA levels, including PrimeTime probes, master mixes, and primer assays. Learn more about the features, benefits, and …eBlocks Gene Fragments are double-stranded DNA fragments of 300–1500 bp in length that are typically shipped in 1–3 business days. They are uniquely suited for high-throughput screening of multiple constructs. IDT offers fragments without flanking (i.e., universal adapter) sequences at no extra cost. With no flanking …The curves represent the theoretical yield for different lengths of oligos based on a coupling efficiency of 99.4% (IDT Oligos, n = 126) and 99.1% (other suppliers, n = 134 from three different suppliers) using the formula: percent full length product = (eff ) (n-1)*100 where eff = coupling efficiency (for example, 99.4% = 0.994) and (n–1) …xGen DNA Library Prep Kit EZ and EZ UNI. Low input, high complexity—up to 3x fewer duplicates from 1 ng of DNA. Improved yield for enrichment—specially formulated PCR master mix boosts yield from a minimal number of PCR cycles. High multiplex capability—pre-plated UDI primers enable multiplexing of up to 1536 …oPools Oligo Pools. Affinity Plus DNA & RNA Oligonucleotides. SameDay Oligos. Rapid HPLC Oligos. HotPlates Oligo Service. Ultramer DNA Oligos. Megamer single-stranded DNA (ssDNA) fragments. TruGrade DNA Oligos.Overview. Polymerase chain reaction (PCR) is a core and widely used laboratory method. An enhancement of this method, qPCR (quantitative PCR, also known as real-time PCR) measures the amplification of DNA in real time and not at the end of cycling like conventional PCR. Together these applications have contributed to … ….

Integrated DNA Technologies, Inc. ( IDT ), headquartered in Coralville, Iowa, is a supplier of custom nucleic acids, serving the areas of academic research, biotechnology, clinical diagnostics, and pharmaceutical development. IDT's primary business is the manufacturing of custom DNA and RNA oligonucleotides (oligos) … Custom primers. Primer design is key for generating high-quality PCR results. IDT offers a variety of custom primers and easy-to-use primer design tools to help ensure that you generate the primers you need to drive your research forward. qPCR solutions. Overview. Ideal conditions for standard DNA oligonucleotides. IDT has tested the stability of oligonucleotides following various storage conditions. The results of these studies indicate that the most stable temperature at which to store a standard DNA oligonucleotide is –20°C. An oligo stored at –20°C is stable for at least 24 months …Ideal conditions for standard DNA oligonucleotides. IDT has tested the stability of oligonucleotides following various storage conditions. The results of these studies indicate that the most stable temperature at which to store a standard DNA oligonucleotide is –20°C. An oligo stored at –20°C is stable for at least 24 months …Certificates of analysis. The certificate of analysis (COA) issued by IDT Quality Assurance provides test results that show product specifications have been met. Download your certificate of analysis by searching for the batch or lot number. For components of a kit, enter the batch or lot number for the component (s) of interest.Figure 1. Melt curves from qPCR of CFTR gene. (A) An amplicon from CFTR exon 17b reveals a single peak following melt curve analysis, while (B) an amplicon from exon 7 produces 2 peaks, is often interpreted as representing multiple amplicons, when in this case, there is only one amplicon generated (Figure 2B). …For PCR primer design, IDT recommends that you aim for PCR primers between 18 and 30 bases; however, the most important considerations for primer design should be the T m value and on-target binding efficiency. Primers should also be free of strong secondary structures and self-complementarity. … OligoAnalyzer™ Tool. Understand the expected behavior of your oligos before you order them. Quickly see GC content, melting temperature, and more. Identify secondary structure potential. Minimize dimerization. Use NCBI Blast. Please sign in to use IDT’s custom online ordering tools. If you don’t yet have an IDT account, join the IDT community! Create your free account today and enjoy unlimited access to our innovative web tools, streamlined ordering, and expert educational content. Trademarks contained herein are the property of Integrated DNA …The xGen Methyl-Seq DNA Library Prep Kit workflow constructs libraries from single-stranded, bisulfite-converted DNA fragments. The Adaptase step simultaneously performs end repair, tailing, and ligation of the R2 Stubby Adapter to the 3’ end of each fragment. The extension step produces a uracil-free strand and the ligation … Idtdna, [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1], [text-1-1]