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reagent Product List and Ranking from 111 Manufacturers, Suppliers and Companies | IPROS GMS

Last Updated: Aggregation Period:Feb 18, 2026~Mar 17, 2026
This ranking is based on the number of page views on our site.

reagent Manufacturer, Suppliers and Company Rankings

Last Updated: Aggregation Period:Feb 18, 2026~Mar 17, 2026
This ranking is based on the number of page views on our site.

  1. ビジョンバイオ Fukuoka//Testing, Analysis and Measurement
  2. KANTO CHEMICAL CO., INC. Biochemical Dept Tokyo//Chemical
  3. ファルマ Tokyo//others
  4. 4 null/null
  5. 5 キアゲン Tokyo//others

reagent Product ranking

Last Updated: Aggregation Period:Feb 18, 2026~Mar 17, 2026
This ranking is based on the number of page views on our site.

  1. Foreign Substance Identification Group (Bloodstain Identification Reagent) [Simple determination by just dropping the reagent] ビジョンバイオ
  2. New fixing solution "Artefix" that does not contain formaldehyde. ファルマ
  3. Reagent: Karl Fischer Reagent Chem Aqua
  4. 4 Bloodstain (blood residue) test / bloodstain identification reagent ビジョンバイオ
  5. 5 RAT-NMP reagent 東レテクノ 技術部

reagent Product List

91~120 item / All 251 items

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Digital PCR kit (reaction reagents)

Using enzyme reaction reagents tailored to the type of nucleic acid being quantified, we achieve efficient and highly sensitive PCR reactions.

Single or multiplex digital PCR may have measurement results influenced by the reagents used. This product series includes master mix reaction reagents optimized to deliver the best performance on nanoplates, whether for copy number variation analysis, mutation analysis, detailed gene expression analysis, or genotyping. Using these reagents improves the accuracy, specificity, and sensitivity of measurements.

  • Other bio-related products and services
  • reagent

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QuantiNova Rev Transcription Kit

Reverse Transcriptase | QuantiNova Reverse Transcription Kit

■Rapid cDNA synthesis for highly reproducible 2-step real-time PCR ■Includes a genomic DNA removal kit to suppress artifact amplification ■cDNA synthesis in 20 minutes ■Includes internal control RNA *For more details, please download the PDF or feel free to contact us.*

  • Real-time PCR
  • reagent

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QuantiTect Rev Transcription Kit

Reverse Transcriptase | QuantiTect Reverse Transcription Kit

■Rapid synthesis of high-sensitivity 2-step real-time RT-PCR cDNA for gene expression analysis ■Includes a genomic DNA removal kit to suppress artifact amplification ■cDNA synthesis in 20 minutes *For more details, please download the PDF or feel free to contact us.*

  • Real-time PCR
  • reagent

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Deparaffinization Solution

Paraffin removal reagent that does not require organic solvents such as xylene.

【Features】 ■ No need for pelletization of samples or removal of supernatant containing paraffin ■ Direct degradation with Proteinase K after paraffin dissolution ■ Easy visualization of paraffin dissolution solution with blue tracking dye ■ Minimizes sample loss and improves nucleic acid recovery *For more details, please download the PDF or feel free to contact us.

  • Other Nucleic Acid/DNA Research
  • reagent

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Nucleic Acid Purification Reagent "AllPrep DNA/RNA FFPE Kit"

Simultaneous purification of genomic DNA and total RNA from the same formalin-fixed paraffin-embedded tissue fragment. Achieving comprehensive analysis of DNA and RNA.

**Features** - Separation and purification of DNA and RNA from the same FFPE sample using a special dissolution method. - Realization of cross-link removal while avoiding fragmentation risks through incubation conditions optimized separately for DNA and RNA. - Elution of DNA in 30 μL and RNA in 14 μL using MinElute spin columns. - Option to select RNA with or without small RNA. - Partial automation with QIAcube Connect. *For more details, please visit the URL below or feel free to contact us.* https://www.qiagen.com/ja-jp/products/discovery-and-translational-research/dna-rna-purification/multianalyte-and-virus/allprep-dnarna-ffpe-kit

  • reagent
  • reagent

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Astra Blue FM (C.I. 48048)

10g for microscope use! Soluble in water (0.5%), dissolve 0.1g in 97.5ml of water and 2.5ml of glacial acetic acid.

"Astrablue FM (C.I. 48048)" is a cellulose dye reagent that is soluble in water (0.5%). It comes in a 10g package for microscopy, with a molar mass (M) of 1068.75 g/mol. Dissolve 0.1g in 97.5ml of water and 2.5ml of glacial acetic acid. Please feel free to contact us for inquiries. 【Product Overview】 ■ 10g for microscopy ■ Chemical formula: C47H52CuN14O6S3 ■ Molar mass (M): 1068.75 g/mol ■ WGK1 ■ CAS number: 82864-57-1 ※ For more details, please refer to the PDF document or feel free to contact us.

  • Fine chemicals (compounds, derivatives, catalysts, etc.)
  • reagent

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Blocking reagent "ROTI Block"

500ml, 10 times concentrated and ready to use! A suitable diluent as a basic solution for immunochemical detection.

"ROTI Block" is a protein-free blocking solution for all blotting and hybridization systems. It is available in a 500ml, 10x concentrated form that is ready to use. It is also suitable as a basic dilution for immunochemical detection. Please feel free to contact us for inquiries. 【Product Overview】 ■ 500ml, 10x concentrated, ready to use ■ Density (D): ~1.086g/cm3 ■ Boiling point (bp): ~100℃ ■ Storage temperature: +15 to +25℃ ■ Transport temperature: Ambient temperature ■ WGK1 *For more details, please refer to the PDF document or feel free to contact us.

  • reagent
  • reagent

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Bovine Serum Albumin (BSA) Fraction V <Biotin-Free>

≥98%, for biochemical and molecular biology use! The process is carried out in a closed system.

"Bovine Serum Albumin (BSA) Fraction V" is excellent as a blocking and stabilizing reagent in all biotin/streptavidin mediated detection systems. Recommended when BSA of Australian or New Zealand origin is required. The purification of albumin uses extensive heat shock/diafiltration methods, and the process is conducted in a closed system. 【Features】 ■ Biotin-free ■ NZ-origin ■ Extensive heat shock/diafiltration methods used for albumin purification ■ Process conducted in a closed system. *Other variations are also available, including fatty acid-free, IgG-free, protease-free, of US and European origin, for cell biology, protein analysis, and molecular biology, etc. *For more details, please refer to the PDF document or feel free to contact us.

  • serum
  • reagent

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Lysozyme

≥45,000 FIP U/mg, freeze-dried! The stability of the solution at pH 4-5 is several weeks at +4°C and several days at room temperature!

"Lysozyme" is a high-quality product for molecular biology. It is a freeze-dried powder that does not contain salt or albumin, making it suitable for the dissolution of bacteria in DNA preparation. It preferentially hydrolyzes the β-1,4-glycosidic bond between N-acetylmuramic acid and N-acetylglucosamine. The freeze-dried product is stable for several years at +4°C and -20°C, with solution stability at pH 4-5 lasting several weeks at +4°C and several days at room temperature. 【Features】 ■ Freeze-dried powder that does not contain salt or albumin ■ High-quality product for molecular biology ■ Derived from egg white, albumin-free ■ Preferentially hydrolyzes the β-1,4-glycosidic bond between N-acetylmuramic acid and N-acetylglucosamine *For more details, please refer to the PDF document or feel free to contact us.*

  • Other Nucleic Acid/DNA Research
  • reagent

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Induction of lung progenitor cells from human iPS cells and formation of alveolar organoids.

We confirmed the induction of lung progenitor cells from human iPS cells using "PG-004," and further verified the formation of alveolar organoids from those cells.

In the process of inducing differentiation of lung progenitor cells from human iPS cells, Noggin was used in the anterior foregut induction step. As an alternative to Noggin, "PG-004" was used, and the differentiation induction efficiency of anterior foregut cells and subsequently induced ventral anterior foregut cells and lung progenitor cells was compared. After maintaining and proliferating human iPS cells (HILC01 strain) in commercially available medium (mTeSR Plus-cGMP) in an undifferentiated state, a stepwise differentiation induction was performed using the collected undifferentiated iPS cells. As a result, "PG-004" showed a concentration-dependent increase in the induction efficiency of each cell type, and particularly, results equivalent to Noggin were obtained in the induction efficiency of ventral anterior foregut and lung progenitor cells. [Summary] ■ Stepwise differentiation induction of endodermal cells, anterior foregut cells, ventral anterior foregut cells, and lung progenitor cells. ■ Formation of alveolar organoids was also confirmed using lung progenitor cells created through the differentiation induction process with "PG-004." *For more detailed test results, please download the materials from the link below.

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Induction of differentiation from iPS cells to NKT cells

Introduction of results on the differentiation induction from iPS cells to hematopoietic stem progenitor cells.

We conducted experiments to promote the differentiation of iPS cells into hematopoietic stem progenitor cells (HSPC) using "PG-007," "PG-008," and "PG-010," which can be utilized in the differentiation induction process into NKT cells. We compared the productivity, differentiation induction efficiency of HSPC, as well as the productivity, differentiation induction efficiency, and functionality of NKT cells, with control conditions using existing methods such as VEGF, CHIR99021, and TPO. As a result, the differentiation induction process was shortened by one day, and more than twice the number of HSPC cells was obtained compared to existing methods. [Summary of Results] ■ "PG-007" demonstrated sufficient effect at one-tenth the concentration of VEGF, "PG-008" at one 2500th the concentration of CHIR99021, and "PG-010" at one-fifth the concentration of TPO. ■ The differentiation efficiency into NKT cells and the functionality of the obtained NKT cells were equivalent to the control conditions, while the number of NKT cells obtained significantly increased. *For more detailed test results, please download the materials from the link below.

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Create organic molecules freely with a new reaction!

Keywords: Organic synthesis, silicon, halogen, catalyst, radical

Organic synthesis is one of the scientific technologies that supports material civilization, and it is used in the production of various products and materials that are beneficial to our lives, such as fuels, oils, fibers, rubber, resins, pharmaceuticals, and food additives. An essential component of organic synthesis is the "reaction," which transforms one molecule into another. In our laboratory, we conduct research with the goal of "developing new reactions that are useful for organic synthesis." In reaction development, we aim to efficiently produce only what we want and to create it in an environmentally friendly manner without waste from readily available raw materials. We also emphasize the originality of our research and chemical discoveries, focusing on the development of novel reactions that have not been seen before, rather than merely improving existing reactions. Various reagents and catalysts are used in organic synthesis, but our laboratory pays particular attention to the reactivity of silicon compounds and halides, as well as the catalytic effects of platinum and palladium. With the aim of making new discoveries, we engage in reaction development with excitement every day.

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Development of biofuel production using microalgae

Keywords: Microalgae, biofuels, renewable energy, decarbonization, carbon neutrality

As environmental changes progress, promoting decarbonization towards the realization of a sustainable society has become a global challenge. We are developing biofuels using microalgae with the aim of creating carbon-neutral renewable energy. The microalga Nannochloropsis accumulates lipids that can reach up to 50% of its cell content and can be cultivated at high densities, which allows us to develop technology for the efficient and high-yield production of lipids using this alga. Meanwhile, we are also advancing the development of an "extracellular production method" for free fatty acids using cyanobacteria, another type of microalgae. The intracellular production method, which involves accumulating fuel substances within the cells, consumes a tremendous amount of energy during processes such as harvesting, drying, and extracting the fuel substances. In contrast, the extracellular production method is expected to significantly reduce costs and has the advantage of being able to produce fuel substances in quantities that exceed the cell volume. The lipids and free fatty acids obtained from the algae can be converted into diesel fuel and other products.

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Create molecules that color sugar.

Keywords: analytical reagents, molecular recognition, supramolecular chemistry, metal complexes, nanoparticles, luminescence, dyes

Various types of sugars exist within living organisms. Each of these plays an essential role in maintaining life and is constantly circulating within the body. Therefore, an imbalance of sugars in the body directly leads to serious diseases that threaten us today (e.g., diabetes). In other words, the development of technology to measure sugar levels is crucial for the early detection of bodily disorders. To develop such technology, I am designing "analytical reagents," which are molecules that glow when they bind to sugars. In my research, I am developing analytical reagents with a simple structure and excellent detection capabilities by using various frameworks (organic dyes, metal complexes, supramolecular complexes, nanoparticles, etc.) as a foundation (Figure 1). So far, I have successfully developed a supramolecular complex-type analytical reagent that specifically fluoresces for D-glucose (blood sugar) among the numerous sugars (Figure 2). I believe that this technology will lead to the development of a diagnostic system for the early detection of diabetes.

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Antibodies and Related Reagents Catalog

TCI has also started antibodies.

The "Antibodies and Related Reagents Catalog" is a brochure that summarizes the antibody products from Tokyo Chemical Industry. It includes anti-glycan antibodies, anti-influenza virus antibodies, anti-6xHis antibodies, secondary antibodies, and their labeled forms. Related assay substrates and staining agents are also included. [Contents] ■ Anti-glycan antibodies ■ Anti-Protein A antibodies ■ Anti-influenza virus antibodies ■ Anti-Endo-M antibodies ■ Anti-6xHis antibodies, etc. *For more details, please refer to the PDF document or feel free to contact us.

  • Contract manufacturing
  • others
  • Chemicals
  • reagent

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DualSeal - High airtight double cap reagent in a bottle

We provide bottles with special caps that allow you to safely dispense liquid pharmaceuticals that are sensitive to moisture and air.

At Tokyo Chemical Industry, we offer the following liquid product range in bottles equipped with a specialized cap (DualSeal) that maintains high airtightness. The specialized cap (DualSeal) allows for the extraction of liquid chemicals without exposure to moisture or air. 【Products】 ■ Volatile gas solutions ■ Metal salt solutions ■ Dehydrated solvents ■ Organometallic reagents

  • Chemicals
  • Contract manufacturing
  • reagent

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Novabiochem(R) Peptide Synthesis Reagent Product Guide

The product specifications for 20 standard Fmoc amino acids have been renewed!

This catalog is a product guide for the high-quality brand of peptide synthesis reagents, "Novabiochem(R)." By setting stricter product standards for standard Fmoc amino acids used in peptide synthesis, we have made it possible to use our products with greater confidence, from basic research to pharmaceuticals, cosmetics, and contract synthesis. We offer a wide range of packaging options, from small sizes to bulk sizes. [Contents (excerpt)] ■ Major Fmoc amino acids ■ Pseudoproline dipeptides ■ Coupling agents ■ Resins for solid-phase synthesis ■ History of Novabiochem innovations *For more details, please refer to the PDF document or feel free to contact us.

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Simple screening reagent "TTC solution"

Established a simple and rapid screening method (TTC method) for E. faecalis and E. faecium!

The "TTC solution" is a simple screening reagent that establishes a rapid screening method (TTC method) for E. faecalis and E. faecium using the reduction ability of 2,3,5-triphenyltetrazolium chloride (TTC). TTC is originally white, but in physiologically active tissues, it is reduced by dehydrogenase enzymes to form an insoluble red compound called TPF (1,3,5-triphenylformazan). However, no color change occurs in tissues that lack activity. Various enzymes are involved in the reduction of TTC to TPF, including succinate dehydrogenase and flavin enzymes from the electron transport chain. 【Usage Instructions】 1. Collect one colony of bacteria grown on sheep blood agar at 37°C for 24 hours using a sterile swab. 2. Add 1-2 drops of TTC solution to the sterile swab that collected the colony. 3. Let it sit at room temperature for 2 minutes. *For more details, please download the PDF or feel free to contact us.*

  • Other research reagents
  • reagent

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Spot indole reagent

Detection of indole production by intestinal bacteria and certain anaerobic bacteria!

The "Spot Indole Reagent" is a product that demonstrates the ability of specific bacteria to decompose the amino acid tryptophan and convert it into indole, accumulating it in the medium. In the spot test, indole binds to p-dimethylaminocinnamaldehyde (DMACA) in an acidic pH within the filter paper matrix, producing a blue to blue-green compound. In a positive result, a color change from blue to blue-green appears in the bacterial smear sample within 2 to 3 minutes. If there is no reaction, it is considered negative. 【Specifications】 ■ Product Number: SG-SPOTIND-5 ■ Volume: 5mL *For more details, please download the PDF or feel free to contact us.

  • Other research reagents
  • reagent

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Waters Analysis Standards & Reagents

By providing readily available standard materials and reagents, we achieve improved lab productivity, reduced waste, and enhanced reliability of analyses.

To achieve the highest quality in instrument analysis, analytical standards and reagents are essential. Waters Corporation, which has been addressing this issue for some time, has launched a new business for the manufacturing and certification of analytical standards and reagents.

  • Analytical Equipment and Devices
  • reagent

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Mycotoxin Poison Testing Series "Veratox Aflatoxin"

Rapid quantitative testing! A test that provides results in 5 minutes without the need for special training.

"Belatox AflaToxin" is a CD-ELISA method that uses a micro-well format for the control of aflatoxins and for comparing and testing samples through direct competitive assays. No special training is required, and the chemical extraction process can be eliminated. An optical density reader (microwell reader) can provide objective judgments and record numerical measurements. All reagents necessary for sample extraction testing are included. 【Features】 ■ Simple operation for rapid results (results available in 5 minutes) ■ Up to 40 tests possible with one kit ■ Complete quantitative results ■ Results equivalent to HPLC method ■ USDA-GIPSA certification #2012-010, AOAC-RI certification #050901 For more details, please refer to the catalog or feel free to contact us.

  • Food Testing/Analysis/Measuring Equipment
  • Other inspection equipment and devices
  • reagent

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Protein separation reagent "AquaFirmus"

Chemically stable and non-specific protein low adsorption type! New solid phase support for affinity resin.

"AquaFirmus" is a novel affinity resin-based solid-phase support that can be used with a wide range of organic solvents. Thanks to the newly developed highly hydrophilic monomer, it possesses high hydrophilic properties that suppress non-specific protein adsorption, along with the chemical stability characteristic of synthetic resins. Additionally, we also offer "AquaFirmus 2000," which is chemically stable, has low non-specific protein adsorption, and can capture protein complexes due to the introduction of longer spacers. 【Features】 ■ Low non-specific protein adsorption due to high hydrophilicity ■ Usable with a wide range of organic solvents ■ Stable under general organic reaction conditions (including protective conditions with 1N NaOH and TFA) ■ Washable with alkali or acid ■ Improved target capture efficiency achieved through high ligand density *For more details, please refer to the PDF document or feel free to contact us.

  • Separation device
  • Oil-water separator
  • Solid-liquid separation filter
  • reagent

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Cell adhesion prevention reagent "On-chip T buffer"

Prevent cell adhesion and minimize cell loss! It has a coating effect that prevents cell adhesion to chips and tubes.

The "On-chip T buffer" is a cell wash and recovery solution that includes a cell non-toxic through-pass, preventing cell loss due to processes such as cell washing and leukocyte separation from peripheral blood. Simply coating chips or tubes with this product can prevent loss due to cell adhesion. It minimizes losses from cell washing and can be used as a washing solution for various applications. [Examples of Use] ■ Cell washing solution for various analyses ■ Washing solution during leukocyte separation ■ Cell staining solution ■ Adding about 0.5% BSA further prevents loss and acts as a blocking agent *For more details, please refer to the PDF document or feel free to contact us.

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Visualizing the effectiveness of quicklime in infectious disease control in livestock production: 'Lime Check'

Lime Check, a reagent for confirming the use of quicklime in epidemic prevention.

Visualizing the effectiveness of slaked lime in measures against infectious diseases such as avian influenza and swine fever on livestock farms. 'Lime Check' is a liquid reagent that confirms the effectiveness of slaked lime through color development. The slaked lime spread in livestock farms gradually transforms into calcium carbonate over time, losing its disinfecting effect; however, both are white powders, making it impossible to visually confirm the effectiveness of disinfection. By dropping Lime Check onto slaked lime, it is possible to instantly determine the disinfecting effect with a visual cue similar to that of a traffic light: - Blue: Sufficient disinfecting effect, - Yellow: Decreased disinfecting effect, - Red: No disinfecting effect.

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  • Other laboratory equipment and containers
  • reagent

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[Analysis Case] Qualitative Analysis of Organometallic Complexes under Atmosphere Control

Mass spectrometry using TOF-SIMS is possible under conditions that are not affected by oxidation.

Titanium tetraalkoxide is an essential reagent for the Katsuki-Sharpless asymmetric epoxidation and is affected by oxidation in the atmosphere. In this case, we present an investigation using TOF-SIMS on how titanium tetraalkoxide (titanium tetra-isopropoxide) changes under controlled atmosphere and after exposure to air. In MST, the evaluation of the complex can be performed without the influence of atmospheric oxidation due to atmosphere control. Measurement method: TOF-SIMS Product fields: Biotechnology, Pharmaceuticals, Cosmetics, Daily necessities Analysis purpose: Deterioration investigation, Reliability assessment For more details, please download the materials or contact us.

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DNA/RNA extraction reagent from plant samples 'ChloroPure'

DNA/RNA extraction from plant samples such as fresh leaves, freeze-dried leaves, and powdered seeds using SPRI magnetic beads.

ChloroPure is a kit for simultaneously extracting and purifying DNA/RNA or total RNA only from plant samples (fresh leaves, freeze-dried leaf punches, powdered seeds, etc.). Plants contain a variety of polysaccharides and secondary metabolites, which make nucleic acid extraction challenging; however, ChloroPure enables the extraction of 7 μg of nucleic acids from a sample of 40 mg (or three 6 mm punches of freeze-dried leaves). It is compatible with the automation of Beckman Coulter's Biomek series automated pipetting systems, achieving high-throughput purification of 96 samples in 45 minutes after the centrifugation step following the lysis process. - Simultaneous extraction of DNA/RNA or RNA from 40 mg of plant leaves or seeds - Stable extraction is possible from leaves and seeds of cotton, sunflower, canola, and more *For more details, please refer to the PDF document or feel free to contact us.

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CleanSEQ purification reagent after Sanger sequencing reaction.

Purification after Sanger sequencing reaction

CleanSEQ is a fluorescent dye terminator removal purification kit used after Sanger sequencing reactions. Sanger sequencing reaction kits are expensive and are generally used in a diluted form. However, dilution can lead to reduced fluorescence intensity, resulting in decreased sequence read lengths. CleanSEQ allows for high purification yields, which can enhance the signal strength during sequencing. - Efficient removal of unreacted fluorescent dyes and primers - Increased fluorescent signal strength and improved sequence read lengths *For more details, please refer to the PDF document or feel free to contact us.

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Reagent for DNA size selection "SPRIselect"

DNA fragment size selection reagent kit

SPRIselect is a kit that allows for the easy recovery of DNA fragments of specific lengths ranging from 150 to 800 bp without the need for cutting agarose gels. By adjusting the mixing ratio of the DNA solution and the SPRIselect reagent, it utilizes the property that the size of DNA fragments binding to magnetic beads can be varied, allowing for the selective recovery of desired fragment sizes. The unique purification protocol using SPRI magnetic beads is optimized, completing manual experiments for double size selection in 20 minutes for 8 samples and 25 minutes for 24 samples. It is also compatible with automation using Beckman Coulter's Biomek series automated dispensing system, achieving high-throughput processing of 48 samples in 51 minutes and 96 samples in 1 hour. - Selectively recover DNA fragments of arbitrary sizes from 150 to 800 bp - High reproducibility achieved through stringent quality control *For more details, please refer to the PDF document or feel free to contact us.

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