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One of the most widely used methods of analyzing gene expression is quantitative PCR (qPCR) following cDNA synthesis. qPCR, also called real-time PCR, uses a fluorescent reporter molecule with a primer pair to measure target nucleic acid amplification during PCR cycling. Explore IDT’s qPCR products that may be used …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 … 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 ... PrimeTime qPCR Primer Assays. The same primer pairs found in the PrimeTime qPCR 5' Nuclease Assays. Forward and reverse primers, mixed and delivered in a single tube or plate well. Compatible with SYBR ® Green, EvaGreen ®, and other intercalating dyes, where no probe is needed. Available in tubes or 96-well plates.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. For research use only. Not for use in diagnostic procedures.

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.

IDTE (1X TE solution) IDTE (10 mM Tris, 0.1 mM EDTA) is our recommended solution for resuspending and storing single-stranded DNA and RNA oligos. It has been shown to offer the most stability for the longest duration when compared to oligos stored dry or in water. IDTE is available at pH 7.5 or pH 8.0.DNA oligos. First-time purchase of 25nm DNA oligos, limited to quantities 4-10. Expires: April 30, 2024. Promo code: 25nm-50. Order Today.

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 …PrimeTime qPCR Primer Assays. The same primer pairs found in the PrimeTime qPCR 5' Nuclease Assays. Forward and reverse primers, mixed and delivered in a single tube or plate well. Compatible with SYBR ® Green, EvaGreen ®, and other intercalating dyes, where no probe is needed. Available in tubes or 96-well plates.© 2024 Integrated DNA Technologies, Inc. Trademarks contained herein are the property of Integrated DNA Technologies, Inc. or their respective owners, and may be ...Place your order online. Quick Self Service ordering is available through our web offerings using the link below. If you haven’t already, it’s easy to get started—simply register your account to begin ordering today. Are stock or pre-designed products what you’re looking for? If so, use the link below to order by part number. 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.

Mixed bases can be used for creating pools of oligos that include matches to a variable or unknown template sequence. They can also be used to create diversity in clone libraries and in site directed mutagenesis. Two types of randomization are available—standard and custom mixed bases, both of which can be ordered …

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.

Complete workflow for hybridization capture research experiments. The xGen cfDNA & FFPE DNA Library Prep v2 MC Kit was designed to work seamlessly with xGen hybridization capture probes and reagents (Figure 2). Whether your project requires whole exome sequencing or custom panels, IDT has the capture solutions for you.The Alt-R S.p. HiFi Cas9 Nuclease V3 offers improved specificity over wild-type Cas9, greatly reducing the risk of off-target cutting events. This Cas9 variant also preserves the high level of editing efficiency expected from a Cas9 nuclease, maintaining 90–100% on-target editing activity at most sites.IDTE (1X TE solution) IDTE (10 mM Tris, 0.1 mM EDTA) is our recommended solution for resuspending and storing single-stranded DNA and RNA oligos. It has been shown to offer the most stability for the longest duration when compared to oligos stored dry or in water. IDTE is available at pH 7.5 or pH 8.0.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 …Digital PCR (dPCR) provides the absolute amount of a target DNA. Properly designed assays can be used to investigate rare alleles, rare microRNAs, copy number variations, and low abundance transcripts. Digital PCR applications span many scientific fields, from liquid biopsy analysis for oncology research to viral …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. …

A wide variety of modifications can be incorporated into an oligo at the time of synthesis. Some modifications, however, must be attached after synthesis, using NHS Ester chemistry. These post-synthesis modifications often result in lower yields, as they require HPLC purification. For detailed information about the modifications …For effective CRISPR editing, proper design of sgRNA sequences is key to achieving high on-target potency while also resulting in reduced off‑target activity. Following a few simple rules will help accomplish this. CRISPR genome editing technology utilizes a Cas enzyme and a guide RNA (gRNA) to generate …Vortex briefly. Incubate at approximately 50°C for 15–20 min. Heating the tube will ensure the solvent comes in contact with the tiny pellet, even if it is stuck to the side of the tube. Thus, this step will increase the likelihood that the entire pellet will be resuspended. Briefly vortex and centrifuge.Oligo modifications. Choose from a variety of modifications and mixed bases that can be incorporated at 5', internal, or 3' positions of primers or probes to improve PCR analysis in regions of complexity; can also be incorporated into oligonucleotides designed for custom applications. Buy IDT's Custom DNA and RNA oligo …Aldevron CRISPR Nucleases. For clients applying gene editing to investigate and treat genetic and inherited diseases, these nucleases provide an accelerated path to the clinic by offering the same product manufactured at research grade and full cGMP, supported by the quality documentation necessary for regulatory filings. …

DNA oligos. First-time purchase of 25nm DNA oligos, limited to quantities 4-10. Expires: April 30, 2024. Promo code: 25nm-50. Order Today.

Alt-R Custom Guide RNAs are ideal for prime editing (pegRNA) projects, CRISPR-Cas13 applications, and most alternative CRISPR-Cas systems. Fast shipping (usually 3–6 business days) A range of modification options. Multi-scale delivery in tubes or plates. We also offer a complete selection of Cas9 guide RNAs (sgRNA, …Oligo modifications. Choose from a variety of modifications and mixed bases that can be incorporated at 5', internal, or 3' positions of primers or probes to improve PCR analysis in regions of complexity; can also be incorporated into oligonucleotides designed for custom applications. Buy IDT's Custom DNA and RNA oligo …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 …Click Sign In on the upper right of any IDT webpage, then click Register to create a new account. Choose a Login Name and Password. Continue by supplying your contact information in the personal information section, then click Save to create your account. Now your name will appear at the top of the IDT webpages. Click your …Frequently asked questions. 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.

Normalized Oligos. With our Normalized Oligos, we’ve made obtaining pure DNA oligos in bulk quantities (up to 10 grams) easy, and many options can now be ordered via our online ordering system! Custom DNA oligos for any application: PCR primer DNA, NGS adapters, synthetic genes, pools and panels. Oligo modifications, …

The IDT guide RNA design tool has 3 modes (accessible using the tabs at the top), as shown in Figure 1 (below). Figure 1. Screen capture of guide RNA design tool options. There are 3 options: “Search for predesigned gRNA,” “Design custom gRNA,” and “CRISPR-Cas9 gRNA checker.”. A library of predesigned …

oPools Oligo Pools are single-stranded DNA sequences that are used for CRISPR library construction, primer pools for multiplex PCR, gene construction, data storage, and FISH analysis. Proprietary DNA synthesis equipment permits rapid, high-quality synthesis of nucleic acids. This platform is the same proprietary synthesis … 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. IDT offers custom and standard oligos, NGS solutions, genes, probes, reagents, and services for various genomics applications. Learn about their products, tools, and blog …IDT provides high-quality, high-fidelity, double-stranded gene fragments and genes, that are available for a variety of workflows and applications such as protein evolution, gene … 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 significant advances in gene ... 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. Alt-R Custom Guide RNAs are ideal for prime editing (pegRNA) projects, CRISPR-Cas13 applications, and most alternative CRISPR-Cas systems. Fast shipping (usually 3–6 business days) A range of modification options. Multi-scale delivery in tubes or plates. We also offer a complete selection of Cas9 guide RNAs (sgRNA, …Research-friendly oligo calculator. Flexible input and advanced parameters to optimize your custom order: Enter your primer or other oligo sequence. Adjust calculation options if desired. Choose a function: Select ANALYZE for easy, one-click access to a T m calculator, GC content calculator, extinction coefficient calculator, …

Oligo modifications. Choose from a variety of modifications and mixed bases that can be incorporated at 5', internal, or 3' positions of primers or probes to improve PCR analysis in regions of complexity; can also be incorporated into oligonucleotides designed for custom applications. Buy IDT's Custom DNA and RNA oligo …This version of Cas9, known as Alt-R Cas9 Nuclease V3, is an excellent choice for most genome editing experiments. If you need a Cas9 with reduced off-target activity that still has the potency (efficiency) of wild-type Cas9, we additionally offer Alt-R HiFi Cas9 Nuclease, which works well when delivered as an RNP, has very high …RNA 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 …Instagram:https://instagram. fay myers motorcycle worldno nonsense neuteringused bike sales near mevp shoes RNA 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 …Alt-R HDR Enhancer V2 improved HDR efficiency in many commonly used human cell lines, including primary T cells [11], Jurkat, HEK-293, HeLa, U2OS, HAP1, K562, iPSCs, Hepa1-6, B16-F12, and H36.12j compared to untreated counterparts (data not shown). This enhancement of HDR efficiency was … captain stevesapcu Researchers identify these differences using a variety of techniques such as polymerase chain reaction (PCR) and quantitative PCR (qPCR). The latter of which often employs a primer-pair and fluorescent probes designed to target a gene and to help identify SNPs. IDT offers predesigned assays, as well as complementary …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 … highland gardens IDTE (1X TE solution) IDTE (10 mM Tris, 0.1 mM EDTA) is our recommended solution for resuspending and storing single-stranded DNA and RNA oligos. It has been shown to offer the most stability for the longest duration when compared to oligos stored dry or in water. IDTE is available at pH 7.5 or pH 8.0.Purchaser is solely responsible for all decisions regarding the use of these products and any associated regulatory or legal obligations. 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 …