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reagent(10) - List of Manufacturers, Suppliers, Companies and Products | IPROS GMS

Last Updated: Aggregation Period:Feb 18, 2026~Mar 17, 2026
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reagent Product List

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Testing reagent "LABScreen Single Antigen"

Coating with a single HLA antigen for which the allergen is known! Antibody specificity identification test reagent.

The "LABScreen Single Antigen" is a kit that sensitively identifies the specificity of anti-HLA antibodies or anti-MICA antibodies present in serum. Each type of bead is coated with a single HLA antigen for which the allele is known. It is capable of detecting DSA (Donor Specific Antibody). 【Features】 ■ LABScreen Single Antigen Class I is coated with single antigens from 31 types of A locus, 50 types of B locus, and 16 types of C locus. ■ LABScreen Single Antigen Class II is coated with single antigens from 36 types of DR locus, 28 types of DQ locus, and 31 types of DP locus. ■ LABScreen MICA Single Antigen is coated with single antigens from 10 types of MICA. *For more details, please refer to the PDF materials or feel free to contact us.

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Virus Antigen Bank

One of the largest in the world! Many researchers use it for the development of vaccines and therapeutic antibodies.

Introducing the "Virus Antigen Bank" of Shinobiological Co., Ltd. We offer over 1,100 recombinant virus antigens, including 50 types of virus antigens and antigens derived from more than 380 strains. Additionally, we have over 6,000 virus-related reagents, including ELISA Kits, which are widely used by researchers around the world for the development of vaccines, immunodiagnostic agents, and therapeutic antibodies. [Details] ■ Recombinant proteins of virus antigens - Derived from 380+ strains - 1,100+ virus antigens ■ Virus antibodies - 500+ antibodies - 20+ neutralizing antibodies *For more details, please refer to the PDF document or feel free to contact us.

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Bovine Serum Albumin (BSA) Fraction V

IgG-free, for biochemistry and molecular biology! The process is conducted in a closed system.

"Bovine Serum Albumin (BSA) Fraction V" is recommended as a blocking and stabilizing reagent in all antibody-mediated detection systems. Available in IgG-free, sourced from New Zealand in sizes of 10g, 50g, 200g, and 500g. The purification of albumin employs extensive heat shock/diafiltration methods. Additionally, the process is conducted in a closed system. 【Product Overview】 ■ Molecular Weight (M): ~66,000 g/mol ■ Storage Temperature: +4℃ ■ WGK1 ■ CAS Number: 9048-46-8 ■ EG Number: 232-936-2 *Other variations are also available. Biotin-free, fatty acid-free, protease-free Origin from the USA and Europe For cell biology, protein analysis, and molecular biology, etc. *For more details, please refer to the PDF document or feel free to contact us.

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Bovine Serum Albumin (BSA) Fraction V

IgG-free, for biochemistry and molecular biology! The process is conducted in a closed system.

"Bovine Serum Albumin (BSA) Fraction V" is recommended as a blocking and stabilizing reagent in all antibody-mediated detection systems. Available in IgG-free, sourced from New Zealand in sizes of 10g, 50g, 200g, and 500g. The purification of albumin uses extensive heat shock/diafiltration methods. Additionally, the process is conducted in a closed system. 【Product Overview】 ■Molecular Weight (M): ~66000g/mol ■Storage Temperature: +4℃ ■WGK1 ■CAS Number: 9048-46-8 ■EG-Nr. 232-936-2 ※Other variations are also available. Biotin-free, fatty acid-free, protease-free. Origin: USA, Europe. For cell biology, protein analysis, and molecular biology, etc. ※For more details, please refer to the PDF document or feel free to contact us.

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[Case Study] On the Use of PNA in Amplicon Sample Preparation

It is possible to estimate higher resolution feed organisms! Introduction of next-generation sequencing analysis examples *Analysis case collection is being distributed.

In our company, when preparing amplicon samples aimed at analyzing the microbial community structure present in plant leaves, we add PNA to suppress amplification from plant mitochondrial and chloroplast origins, resulting in favorable outcomes. Without the addition of PNA, approximately 90% of the acquired data consists of amplification products derived from the host. By adding PNA, we can reduce this to about 10%, allowing for a higher resolution estimation of the target organisms. [Results of condition testing with 4 sample units] ■ Ct1-Ct4: No PNA added ■ Mt1-Mt4: PNA added for mitochondrial blocking ■ Pl1-Pl4: PNA added for chloroplast blocking ■ PM1-PM4: PNA added for both mitochondrial and chloroplast blocking *For more details, please refer to the PDF document or feel free to contact us.

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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.

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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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GenCheckⓇ qPCR Probe Master

No need for complicated reagent preparation! 2× premix type reagents for real-time PCR.

This product is a 2× premix type reagent for real-time PCR. It contains heat-stable DNA polymerase, Mg2+, Passive Reference Dye, and optimized buffers necessary for real-time PCR (fluorescent probe method), allowing it to be used simply by adding template DNA, primer pairs, and probes. The heat-stable DNA polymerase included in this product is prepared for hot start PCR and is activated by a heat treatment of 95°C for 10 minutes. 【Features】 ■ Enables highly specific real-time PCR ■ No complicated reagent preparation required ■ Compatible with various real-time PCR devices (plate type) ■ Passive reference dye is pre-added ■ By adding UNG (Uracil-N-Glycosylase) separately, carryover prevention treatment is possible (UNG is not included in this product) *For more details, please refer to the PDF document or feel free to contact us.

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

≥98%, for biochemical and molecular biology use! The process is conducted 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. Additionally, the process is conducted in a closed system. 【Features】 ■ Biotin-free ■ NZ-origin ■ Extensive heat shock/diafiltration methods are used for albumin purification ■ The process is conducted in a closed system *There are many other variations available, including fatty acid-free, IgG-free, protease-free, and of US or European origin, suitable for cell biology, protein analysis, and molecular biology, etc. *For more details, please refer to the PDF document or feel free to contact us.

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Fasmac: Artificial Gene Synthesis

Everything from order receipt to manufacturing is done within Japan! We significantly reduce the time and effort our customers spend on complicated tasks.

We would like to introduce the artificial gene synthesis from Fasmac Co., Ltd., which we handle. The synthesized sequences will be delivered in a plasmid form after being introduced into a vector as double-stranded DNA. In addition to the standard pUC series vectors from the company, we can also accommodate cloning into specified vectors provided by you. All processes from order to manufacturing are conducted domestically in Japan, and our specialized staff will respond quickly and meticulously. This significantly reduces the time and effort our customers spend on complicated tasks such as PCR, cloning, and sequencing analysis. 【Service Items】 ■ Express Course - Up to 1,500 bp / 1,501 to 3,000 bp / 3,001 to 4,000 bp ■ Standard Course - Up to 1,500 bp / 1,501 to 3,000 bp / 3,001 to 4,000 bp - 4,001 to 6,000 bp / 6,001 to 10,000 bp *For more details, please refer to the PDF document or feel free to contact us.

  • Analytical Equipment and Devices
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Molecular biology-related reagent "Protease K solution"

Perfect for genetic engineering experiments! Easy to prepare in solution form! Long-term stability with refrigeration!

"Protease K solution" is a reagent that efficiently breaks down proteins due to its broad cleavage activity as a type of endopeptidase. 【Features】 ■ Optimal for nucleic acid purification with DNase and RNase below detection limits ■ Recombinant enzyme with minimal lot-to-lot variation ■ Solution type that is easy to dilute ■ Guaranteed enzyme activity of ≧600 U/mL (37 °C, hemoglobin) ■ Long-term storage possible even in refrigeration (2–8 °C) *For more details, please refer to the catalog or feel free to contact us.

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Influenza virus-related reagents

Sino Biological's influenza virus research reagents

The influenza virus is an RNA virus that causes acute respiratory diseases and outbreaks in human populations due to its strong infectivity. According to the WHO, influenza results in approximately 1 billion infections and about 290,000 to 650,000 deaths worldwide each year. Vaccination is the most effective strategy to prevent influenza virus infection and its severe complications. However, the influenza virus is prone to mutation, and the circulating strains vary from year to year. Each year, vaccine manufacturers develop and produce influenza vaccines based on the strains recommended by the WHO. Our company provides comprehensive influenza vaccine development services and production solutions to vaccine manufacturers. We offer a wide range of research reagents for influenza viruses, including influenza vaccine antigens, antibody pairs, neutralizing antibodies, and kits. Additionally, we provide high-quality technical services such as kit development, antigen expression, and antibody development. These products and services are suitable for various vaccine development scenarios, including screening of vaccine candidate strains, preparation of virus seed batches, evaluation of vaccine safety and immunogenicity, and assessment of vaccine protective effects.

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Introduction to Custom Monoclonal Antibody Production Service Case Studies vol. 1

Thanks to our unique antibody production technology, antigens can be set with high flexibility! We will introduce examples of monoclonal antibody production in our article.

This article introduces examples of monoclonal antibody production. The antibody craftsman's monoclonal antibody production service utilizes a unique antibody production technology that does not rely on animals, allowing for a high degree of flexibility in setting antigens. This enables the production of antibodies that can recognize slight differences in antigens or have specific binding sites tailored to the purpose, resulting in antibodies with special specificities that meet specific needs. HuCAL technology has over 10 years of proven results worldwide, having produced 14,000 antibodies. Its success rate over the past three years boasts over 90%, and it is adopted by many pharmaceutical companies and others. [Contents] ■ Examples of monoclonal antibody production (with work overview) ■ Other antibody production examples *Detailed content of the article can be viewed via the related links. *For detailed specifications, please refer to the PDF materials or feel free to contact us.

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Dioxin Rapid Method (Bioassay) "Keilax Assay"

Ideal for self-management of facilities! A globally recognized high-precision, low-cost dioxin measurement method.

The "Kailax Assay" is a groundbreaking and pioneering analytical method for the simple and rapid measurement of dioxins (PCDDs, PCDFs, DL-PCBs). Compared to conventional analytical methods, it provides results more quickly and at a lower cost. It can be used for various purposes, including as an official method, for self-testing, research and development, and screening investigations. Due to its high sensitivity, it is applicable not only to environmental media but also to low-concentration media such as food and biological samples. If necessary, we can provide the results of our validated tests or conduct investigations and tests together. We reduce costs through process shortening using our unique technology. 【Benefits】 - Reduction of waste stockyards - Cost savings - Implementation of sampling inspections - Early detection of abnormalities in plant equipment - Ability to provide three times the analytical data due to its speed and low cost For more details, please contact us or download the catalog.

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Human DNA removal tool 'MolYsis'

Selective enrichment of bacterial and fungal DNA! Human DNA can be removed regardless of sample volume. [Trial campaign in progress]

"MolYsis" is a tool that removes human DNA and concentrates bacterial and fungal DNA from liquid samples. Technically, it is effective in a short series of steps for the selective lysis of blood cells and the quantitative degradation of released human DNA (>99%). After the lysis solution is concentrated by centrifugation, the microorganisms are treated with reagents that break down the cell walls of gram-positive bacteria, gram-negative bacteria, and fungi. It has been clinically evaluated for a wide range of microbial lysis, demonstrating effectiveness against over 200 species of bacteria and 65 species of fungi. From December 1, 2021, to March 31, 2022, Jumatsu Trading will offer a trial kit of "MolYsis Complete5" from this series at a special price. For more details, please check our website's news section (December 1, 2021: Announcement). [Features] - Removes human DNA - Selectively concentrates bacterial and fungal DNA - Removes PCR inhibitors - Dissolves a wide range of bacteria and fungi *For more details, please refer to the PDF materials or feel free to contact us.

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  • Real-time PCR
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Environmental allergen-related reagent "Dust Mite Allergen Measurement ELISA Kit"

For trace measurement of dust mite allergens! A kit for measuring allergen concentration, capable of measuring from flour as well.

The "Dust Mite Allergen Measurement ELISA Kit" is a kit designed to measure the concentrations of the major allergens Der p 1 and Der f 1 or Der 2 from house dust mites and storage mites. By using this kit, you can sensitively detect allergens derived from dust mite bodies or feces, which serve as indicators when assessing contamination levels of dust mite allergens in indoor environments. <NEW> By using the dilution solution (flour) for the dust mite allergen kit, it has become possible to efficiently extract and measure dust mite allergens (Der p 1, Der f 1, Der 2) contained in flour, which was difficult to extract with conventional dilution solutions. 【Features】 - Detection of allergens from dust mite bodies or feces - High-sensitivity quantification using ELISA - High reproducibility with an average C.V. value of less than 5% - All necessary reagents included - Uses a separate plate that can be used in multiple sessions *For more details, please refer to the catalog or feel free to contact us.

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Standard Protocol for Inducing Atopic Dermatitis by "Biosta AD"

This is an introduction to the standard protocol for inducing atopic dermatitis using BioSta AD.

In the atopic dermatitis model using Biosta AD, after destroying the skin barrier with 4% SDS, the product is applied to the back and ear area of the mice at a dose of 100 mg/mouse twice a week. The induction period is approximately 3 weeks (for a total of 6 applications). Ultimately, a total of 600 mg of the product will be applied. In this model, symptoms begin to appear from 1 to 2 weeks after the start of application, with an incidence rate of about 80% observed at 3 to 4 weeks. 【Initial Induction Method】 ○(1) NC/Nga mice (female, from Charles River Japan, aged 10 weeks or older) are anesthetized (with ether), and the back and ear areas are shaved with clippers, followed by the application of an appropriate amount of depilatory agent to remove hair. ○(2) After wiping off the depilatory agent, 100 mg of Biosta AD is evenly applied to the back and ear areas. ○(3) After application, the mice are returned to their breeding cages. For more details, please contact us or download the catalog.

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Sterile Test Reagent BactFinder/FungiFinder

Contributing to cell safety!

Aseptic testing is generally required to be conducted using the final processed product as the test specimen, based on the aseptic testing method specified in the Japanese Pharmacopoeia General Test Method (4.06). This testing method requires a culture period of more than 14 days to obtain results. On the other hand, for specific cell processing products, it is desirable to obtain the results of the aseptic test before administration to the patient. However, due to the time required to obtain results from the pharmacopoeia-compliant aseptic test, it is often the case that test results are determined after administration. Additionally, for specific cell processing products, due to limitations such as the amount of specimen available and the time required for testing, it may not be possible to apply the aseptic testing method compliant with the pharmacopoeia. In such cases, consideration may be given to the "Rapid Microbial Testing Method" (as referenced in the 18th revision of the Japanese Pharmacopoeia). Our company has developed a rapid aseptic testing method using PCR that covers a wide range of microorganisms, including not only those listed in the pharmacopoeia but also environmental bacteria and human-derived bacteria, allowing for detection in a short time.

  • Real-time PCR
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Reagents for Luminex 100/200

Solution for sending samples to the optical system of the system! Each has a capacity of 25 doses.

We would like to introduce the "Reagents for Luminex 100/200" used for the xMAP system that we handle. When using the "Luminex 100/200 System," sheath fluid PLUS is required as the solution to send samples into the system's optical system. Dedicated "Calibration Kit" and "Performance Verification Kit" are used, with each kit providing enough for 25 tests. 【Features】 ■ Uses dedicated "Calibration Kit" and "Performance Verification Kit" ■ Each kit provides enough for 25 tests *For more details, please download the PDF or feel free to contact us.

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Introduction to Custom Monoclonal Antibody Production Service Case Studies vol. 9

Not mediated by animal immunity! An article introducing successful cases of antibodies that distinguish specific oxidized Cys.

DJ-1 is a 21 kDa protein, and we present a successful case of producing antibodies that specifically recognize the oxidized form of the Cys residue at position 106 (C106) of DJ-1. We have attempted to obtain antibodies that specifically recognize the oxidized C106 through the production of polyclonal antibodies via immunization in rabbits and monoclonal antibodies via immunization in mice, but we were unable to obtain the desired antibodies in either case. Here, we introduce a method for producing antibodies that do not involve animal immunization and are selected entirely in vitro, along with the results of verifying the specificity of the obtained antibodies. 【Contents】 ■1. What is DJ-1 ■2. Strategic Screening  ・2-1. Antigen Design  ・2-2. Panning and ELISA Screening  ・2-3. Cross-reactivity Confirmation by ELISA ■3. Western Blotting and Immunoprecipitation ■4. Summary *For detailed content of the article, please refer to the related links. *For detailed specifications, please refer to the PDF document or feel free to contact us.

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Announcement of the Establishment of the Nucleic Acid Medicine API Development Center

[Announcement of New Base Establishment] Opening of a new GMP manufacturing facility for oligonucleotides.

Ajinomoto Bio-Pharma Services and Gene Design will strengthen its contract development and production system from the early stages of development to late stages and market launch by introducing large-scale production facilities. With the establishment of the new site, the production volume per lot will expand to the kilogram level. By combining our production capacity with the mass production technology of the Ajinomoto Group, a flexible and seamless supply system will be established, transitioning from conventional μg manufacturing to over 100 kg. [Overview] - Newly established within the research facility in Ibaraki City, Osaka Prefecture - Combined with the mass production technology of the Ajinomoto Group (AJIPHASE technology) - Establishing a supply system from conventional μg to over 100 kg *For more details, please refer to the PDF document or feel free to contact us.

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Palladium(II) chloride

Introduction of raw materials such as conductive paste, electronic components, and palladium plating!

Palladium(II) chloride is a dark red or dark brown hygroscopic powder. It is slightly soluble in water and ether, and dissolves in water with hydrochloric acid to form a yellow-brown clear solution. Manufactured using high-purity palladium metal with a purity of 99.95% or higher, through a unique method in fully sealed equipment. It maintains a quality that sufficiently meets the standards of Japanese Industrial Standards (JIS-K8154) for reagent grade and has received high evaluations. 【Applications】 ■ Conductive paste ■ Electronic component plating ■ Plating ■ Catalyst ■ Reagent *For more details, please refer to the PDF document or feel free to contact us.

  • Other polymer materials
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Polymer pullulan (standard reagent)

In the field of high polymers with a molecular weight of 1.6 million, we offer a variety of "polymer pullulan (standard reagent)" with a sharp molecular weight distribution! (Newly released in June 2022)

【Features】 ■ Optimal as a molecular weight marker for the polymer field (for aqueous SEC) ■ A variety of standard reagents are available to meet more specific needs within the polymer field (equivalent to molecular weights of 1.2 million, 1.6 million, and 2 million) We also have stock of molecular weight standards that can accommodate smaller quantities beyond these. Please feel free to contact us. ■ The molecular weight distribution is very sharp. ■ Soluble in water, and the aqueous solution is stable.

  • Other analytical and testing equipment
  • Other pharmaceutical intermediates and cosmetic ingredients
  • Fine chemicals (compounds, derivatives, catalysts, etc.)
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n-Butyllithium

When storing, keep it under inert gas! Avoid contact with water and air.

"Normal butyllithium" is a mixture with aliphatic hydrocarbon solvents. Therefore, it falls under the category of hazardous materials, Class 4, Category 1, non-water-soluble petroleum products. Additionally, butyllithium itself has a property of reacting violently with water. We recommend using it within three months. When using, please refer to the SDS and handle it after thorough investigation. 【Properties】 ■Molecular weight: 64.06 ■Solubility: Easily mixes with aliphatic hydrocarbons ■Stability: Stable below room temperature under an inert gas atmosphere *For more details, please refer to the PDF document or feel free to contact us.

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Hirosaki University Technology: Triptansulin Derivative: K23-010

Fluorescent dyes that can be widely used from biological systems to metals.

Triptanslin is known as an antibacterial agent extracted from the plant indigo. The inventors of this invention chemically synthesized triptanslin derivatives that cannot be obtained from natural sources and were investigating the structure-activity relationship regarding antibacterial properties when they discovered that introducing an amino group at the 2-position of triptanslin resulted in strong fluorescence. This invention relates to fluorescent reagents of triptanslin. **Characteristics of Triptanslin Derivatives** - 2-Aminotryptanslin (T2NH2) can be excited at wavelengths in the visible light range with minimal damage to cells and changes its fluorescence color in response to the surrounding environment (polarity). Additionally, through fluorescence resonance energy transfer (FRET) with pyrene, red fluorescence derived from T2NH2 is observed when FRET is on, but in the presence of certain metal ions such as mercury, it becomes FRET-off and changes to blue fluorescence derived from pyrene. - 2-Hydroxytriptanslin emits light in the wavelength range of the biological window (650–900 nm), which has excellent biocompatibility and is less affected by proton dissociation in the excited state and by the absorption of water or biological substances.

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Tohoku Univ. Technology : External stimulus responsive click reaction technology : T21-077

Controling Inverse-Electron-Demand Diels–Alder Reaction with macrocyclic tetrazine

Inverse-Electron-Demand Diels–Alder Reaction(IEDDA), a cyclization reaction between tetrazine and dienophile, is used in various fields from materials science to biological applications due to its fast reactivity and high selectivity. If this reactivity can be controlled, the application range is expected to expand dramatically. A method for controlling the reaction by oxidizing dihydrotetrazine to tetrazine, which is less reactive, has been reported, but there are problems such as the effect of natural oxidation and the inability to respond to stimuli other than oxidation.   The inventors found that the IEDDA reaction can be completely suppressed by derivatizing tetrazine to a macrocyclic structure, and that the reaction proceeds rapidly when the reaction is converted from a cyclic to an acyclic structure by stimulation. The stimuli in the present invention can be selected according to the application, such as light, heat, pH, enzymatic reaction, redox, etc. By using the present invention, it is expected to be applied to the in vivo synthesis of active pharmaceuticals, environmentally responsive drug delivery systems, chemical sensors, nuclear medicine diagnostics, etc.

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Virus denial test reagent "VirFinder"

It is possible to achieve high sensitivity and rapid detection of viruses as described in the law concerning the assurance of safety in regenerative medicine and other related fields!

The gene detection kit VirFinder for virus denial testing can detect eight types of viruses listed in the law concerning the assurance of safety in regenerative medicine and other fields.

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New fixing solution "Artefix" that does not contain formaldehyde.

Non-toxic and not classified as hazardous! Free from irritating odors and tear-inducing effects!

- Lower toxicity compared to formalin. - The mechanism of protein fixation is similar to that of formalin. - Using it as a storage solution after formalin fixation reduces exposure. - The use of formalin can be limited to specific areas. *For more details, please contact us at the URL below (or visit the website of Falma Co., Ltd.). Sample provision is also available. http://www.falma.co.jp/07question/index.html

  • Other experimental consumables
  • reagent

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[Sample available] Nucleic acid extraction reagent / CellEase Plant

[Sample available] It is possible to extract genes from plants and prepare DNA samples in just 9 minutes.

The CellEase(R) Plant nucleic acid extraction reagent for plants enables gene extraction from plants, which was difficult with the conventional CellEase and CellEase II. The protocol is the same as that of the conventional CellEase, and there is no need for complicated purification and separation processes. As a result, DNA samples that can be directly added to the gene amplification reaction (PCR) can be prepared in just 9 minutes. 【Features】 ○ For plants ○ Only 9 minutes ○ No purification required ○ Only temperature control Please contact us for more details.

  • Other research reagents
  • reagent
  • Other purification and extraction
  • reagent

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[Sample available] Nucleic acid extraction reagent / CellEase Blood

[Sample available] Gene extraction from whole blood is possible, and DNA samples can be prepared in just 9 minutes.

The CellEase(R) Blood nucleic acid extraction reagent for whole blood enables gene extraction from whole blood, which was difficult with the conventional CellEase and CellEase II. The protocol is the same as that of the conventional CellEase, eliminating the need for complicated purification and separation processes. As a result, DNA samples that can be directly added to the gene amplification reaction (PCR) can be prepared in just 9 minutes. 【Features】 ○ For whole blood ○ Only 9 minutes ○ No purification required ○ Only temperature control Please contact us for more details.

  • Other research reagents
  • reagent
  • Other purification and extraction
  • reagent

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