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enzyme Product List and Ranking from 26 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.

enzyme 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. 重松貿易 大阪本社 Osaka//others
  2. 三和メック Tochigi//others
  3. 合同酒精 酵素医薬品本部 Chiba//Manufacturing and processing contract
  4. 日本酵研 本社 Osaka//others
  5. 5 ニッポンジーン Toyama//others
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enzyme 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. Yeast Neutral Lactase 'GODO-YNL' 合同酒精 酵素医薬品本部
  2. Cysteine protease 'FabRICATOR Z (IdeZ)' 重松貿易 大阪本社
  3. Decomposing enzyme "Bacillus molasses liquid" 三和メック
  4. 4 Mass Spectrometry (MS) Grade Trypsin RapiZyme 日本ウォーターズ（米国本社 Waters Corporation）　
  5. 5 Enzymes useful for the characterization and analysis of antibody-drug conjugates (ADCs). 重松貿易 大阪本社

enzyme Product List

31～60 item / All 64 items

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Genovis Inc. Immobilized PNGase F

Genovis Inc. Immobilized PNGase F

Rapid and easy removal of N-glycans from antibodies and proteins using a spin column.

Immobilized PNGase F is a product in which the enzyme PNGase F (Peptide N-glycosidase F) is covalently bonded to agarose beads in a spin column format, allowing for the easy removal of N-glycans from antibodies, fusion proteins, and other N-glycosylated proteins. This enzyme is produced by expressing a gene derived from Elizabethkingia meningoseptica in E. coli through recombinant methods. Samples of glycoproteins are incubated with Immobilized PNGase F under standard reaction conditions for 1 hour to overnight, or under denaturing reaction conditions (using RapiGest SF Surfactant) for 15 to 60 minutes. The deglycosylated glycoproteins can then be easily collected by centrifugation. The activity of PNGase F on some glycoproteins may be reduced or inhibited due to steric hindrance. In such cases, longer incubation times or denaturation of the glycoproteins may be necessary.

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  • Other protein analysis
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Cysteine protease "GingisKHAN (Kgp)"

Cysteine protease "GingisKHAN (Kgp)"

Cleavage of the upper region of the human IgG1 hinge! Produces intact and homogeneous Fab and Fc fragments.

"GingisKHAN (Kgp)" is a cysteine protease that cleaves human IgG1 at a specific site upstream of the hinge region, producing intact and homogeneous Fab and Fc fragments. This enzyme is used for the characterization of antibody-based biological therapies using LC-MS, Fc glycan analysis, studies on the effects of bispecific antibodies, affinity and binding strength, as well as the identification of post-translational modifications. [Features] - Cleaves human IgG1 at a specific site upstream of the hinge region - Produces intact and homogeneous Fab and Fc fragments - Used for the characterization of antibody-based biological therapies using LC-MS, Fc glycan analysis, studies on the effects of bispecific antibodies, affinity and binding strength, and the identification of post-translational modifications *For more details, please refer to the PDF document or feel free to contact us.

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  • Other restriction enzymes
  • Research Antibodies
  • Other protein analysis
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Protease 'GingisREX (RgpB)'

Protease 'GingisREX (RgpB)'

Specifically cleaves proteins at arginine! It also cleaves when the adjacent amino acid is proline!

"GingisREX (RgpB)" is an arginine-specific protease that cleaves proteins at the C-terminal of arginine residues. It is capable of cleaving arginine-proline sequences, which are difficult to cleave with other enzymes. This enzyme is useful for peptide mapping, de novo peptide sequencing, and the analysis of post-translational modifications. 【Features】 - Cleavage is possible even when the adjacent amino acid is proline. - Compared to cleavage by trypsin, longer peptides are generated, allowing for separation and identification using high-resolution MS. - Increases options for sample preparation for bottom-up approaches, improving degradation profiles and sequence coverage. - Shows activity over a wide pH range of 5.0-9.0, requires cysteine, but is inhibited by guanidine hydrochloride. *For more details, please refer to the PDF document or feel free to contact us.*

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  • Other restriction enzymes
  • Research Antibodies
  • Other protein analysis
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Protease "OpeRATOR"

Protease "OpeRATOR"

Specifically cleave proteins with O-glycans! Intermediate-level approaches using MS analysis are also possible!

"OpeRATOR" is a specific protease that cleaves the N-terminal residues of Ser and Thr in glycan residues of proteins with mucin-type O-linked glycans. O-linked glycopeptides are generated, allowing for O-linked glycan profiling, peptide mapping, determination of site occupancy, and intermediate-level approaches through MS analysis. 【Features】 ■ Specifically cleaves proteins with O-linked glycans ■ Generates O-linked glycopeptides ■ Enables O-linked glycan profiling, peptide mapping, determination of site occupancy, and intermediate-level approaches through MS analysis ■ Does not digest glycoproteins at N-linked glycan sites *For more details, please refer to the PDF document or feel free to contact us.

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  • Other restriction enzymes
  • Research Antibodies
  • Other protein analysis
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High-accuracy enzyme 'Go-to DNA Polymerase'

High-accuracy enzyme 'Go-to DNA Polymerase'

A "highly reliable (Go-to)" PCR enzyme that combines excellent extensibility while maintaining high accuracy!

The "Go-to DNA Polymerase" we handle is a PCR enzyme that combines α-type DNA polymerase derived from Pyrococcus sp. with a modified elongation enhancer. It possesses 3’→ 5’ exonuclease activity, which allows it to remove incorrectly incorporated nucleotides during the polymerase reaction, making it suitable for applications requiring high accuracy in DNA fragments, such as cloning. Additionally, the modified elongation enhancer improves the shortcomings of α-type DNA polymerase, such as low elongation speed and amplification efficiency. 【Features】 ■ Mixture of α-type DNA polymerase and modified elongation enhancer ■ Faster elongation speed and better DNA amplification efficiency due to the modified elongation enhancer ■ Has proofreading activity, ensuring high accuracy *For more details, please refer to the related links or feel free to contact us.

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High-purity TEV protease suitable for tag cleavage of tag-fused proteins.

High-purity TEV protease suitable for tag cleavage of tag-fused proteins.

Highly pure, array-specific protease is optimal for tag cleavage of fusion proteins!

Tobacco Etch Virus-derived protease (TEV Protease) recognizes a specific 7-amino acid sequence Glu-Asn-Leu-Tyr-Phe-Gln-Gly/Ser and cleaves between Gln and Gly (or between Gln and Ser). This product does not contain glycerol. Additionally, due to its minimal buffer composition that does not include additives such as surfactants, it is suitable for the preparation of samples used in protein science research, such as protein crystallography. 【Features】 - Cleaves tags from target proteins containing the TEV protease recognition sequence - Affinity purification tags (8×His, 6×HN) are added, allowing for easy removal of the enzyme after the reaction - Glycerol-free - Minimal buffer composition without additives such as surfactants - Ideal for sample preparation in protein science research

  • Other Protein Research
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Enzyme 'Bst DNA Polymerase' for isothermal gene amplification technology LAMP method

Enzyme 'Bst DNA Polymerase' for isothermal gene amplification technology LAMP method

Bst DNA polymerase is an enzyme that can be used in the LAMP method. The LAMP method is a technique for amplifying and detecting target DNA or RNA in a short period of time.

This product is an enzyme that has 5'→3' DNA polymerase activity and strand displacement activity, capable of synthesizing new DNA strands while dissociating the hydrogen bonds of the double-stranded DNA template. The heat-stable strand-displacing DNA polymerase does not require the dissociation of double-stranded DNA due to its characteristics, allowing DNA synthesis at a constant temperature, and it is not affected by synthesis inhibition caused by the secondary structure of DNA. 【Features】 ■ Has 5'→3' DNA polymerase activity and strand displacement activity ■ Capable of DNA synthesis at a constant temperature ■ Suitable for synthesizing DNA strands with high GC content ■ Not inhibited by the secondary structure of DNA 【Optimal Reaction Temperature】 60°C to 65°C 【Inactivation Time】*1 80°C for 5 minutes *1 Inactivation temperature when the enzyme stock solution is directly heat-denatured 【Applications】 Applications utilizing strand displacement activity (such as isothermal gene amplification methods)

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Morning Jelly Medical Enzyme Enzyme Jelly

Morning Jelly Medical Enzyme Enzyme Jelly

"Fasting Professionals" × "Doctors" × "Pharmacists Team" jointly developed food enzyme fermented extract jelly, Asa-Jure.

Medical Enzyme Enzyme Jelly Product Name: Asa-Jure Contents: 520g (130g x 4 packs) 4 pouches included: ¥7,800 (tax included) The JAN code is 4573568370077. The manufacturing facility is located in Chiba Prefecture, and the expiration date is 2 years. 1 case contains 20 units. Wholesale sales are now open. Based on a grain fermentation enzyme extract using over 150 types of ingredients, it includes zinc and date syrup (iron and magnesium), which are often lacking in women's diets. Asa-Jure supports "you" looking towards the future. Please enjoy it as a replacement for breakfast.

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Coenzyme Q10 (Coenzyme Q10) High Purity API Health Maintenance Support

Coenzyme Q10 (Coenzyme Q10) High Purity API Health Maintenance Support

Coenzyme Q10 API that helps in the energy production of cells. A natural ingredient that is highly pure and can be supplied stably, making it ideal for health foods and beauty supplements.

Coenzyme Q10 (CoQ10) is an essential coenzyme for energy production in the mitochondria of human cells and is also a powerful antioxidant. It decreases with age, which is why it is widely used in supplements and functional foods aimed at maintaining health, beauty, and fatigue recovery. Our Coenzyme Q10 API is produced in a high-purity and well-controlled manufacturing environment, ensuring a stable supply. It is made from naturally derived raw materials and manufactured in a GMP-certified facility to ensure safety and reliability. Its applications are diverse, including health foods, beauty products, and pharmaceutical ingredients, making it an optimal component for supporting energy metabolism.

  • Cosmetic materials and raw materials
  • Food/beverage functional materials
  • Pharmaceutical materials and carriers
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Superoxide dismutase (SOD) for antioxidant and anti-aging use.

Superoxide dismutase (SOD) for antioxidant and anti-aging use.

Reduces oxidative stress in cells, making it ideal for anti-aging and wrinkle prevention. High-purity SOD powder for beauty and health foods, cosmetics, and functional supplements.

Superoxide dismutase (SOD) is an antioxidant enzyme that efficiently removes superoxide radicals generated within cells, possessing strong antioxidant properties that contribute to aging prevention and cell protection. It is available in light pink to reddish-purple granules or powder form, making it ideal for use in food, cosmetics, and dietary supplements. SOD is expected to suppress oxidative stress in cells and provide various effects such as maintaining skin elasticity, reducing wrinkles, and supporting immune function, making it an essential ingredient in the development of anti-aging related products. Our SOD is of high purity and stability, manufactured in compliance with ISO9001, FSSC22000, and HACCP standards, and serves as a reliable raw material for B2B products. It can be utilized in a wide range of applications, including cosmetics, beauty supplements, functional beverages, and health foods, and flexibly meets customer product development needs.

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Decomposing enzyme "Amino enzyme"

Decomposing enzyme "Amino enzyme"

It enhances nutrient absorption and contributes to increased yields!

"Amino Enzyme" is a decomposing enzyme that has been long-aged and fermented in an optimized environment using Okinawa sugar molasses, fish broth extract, corn fermentation liquid, bamboo shoot fermentation liquid, seaweed extract, bubble water, photosynthetic bacteria, yeast, and lactic acid bacteria. It can balance the proliferation of soil microorganisms and promote the decomposition of organic matter, achieving an increase in fertilizer absorption. 【Features】 ■ Balances the proliferation of soil microorganisms ■ Promotes the decomposition of organic matter ■ Increases fertilizer absorption ■ Quickly absorbs amino acids and trace elements necessary for strawberry cultivation ■ Contributes to increased yield by enhancing fruit size *For more details, please download the PDF or feel free to contact us.

  • Biofertilizer for Agriculture
  • Biofertilizer for Horticulture
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QIAGEN OneStep RT-PCR Kit

QIAGEN OneStep RT-PCR Kit

Reverse Transcriptase | Rapid cDNA Synthesis by High-Sensitivity and Specific One-Step RT-PCR

■Rapid cDNA synthesis using high-sensitivity and specific one-step RT-PCR ■Q-Solution included to improve amplification for QC-rich targets and templates with secondary structures *For more details, please download the PDF or feel free to contact us.*

  • Real-time PCR
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【Did You Know】Sugar-Decomposing Enzymes <Enzyme Function Series>

【Did You Know】Sugar-Decomposing Enzymes <Enzyme Function Series>

Introducing maltase, sucrase, and lactase! An explanation of the absorption mechanism of monosaccharides.

This article introduces "sugar-decomposing enzymes - maltase, sucrase, and lactase." Many enzymes are known to break down carbohydrates, starting with amylase. Maltase, sucrase, and lactase are enzymes involved in the decomposition of carbohydrates. For details on the decomposition reactions and activity measurement methods of each enzyme, please refer to the sections on maltase, sucrase, and lactase. *You can view the detailed content of the article through related links and catalogs. For more information, please feel free to contact us.*

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We will explore the mechanisms and applications of enzymes!

We will explore the mechanisms and applications of enzymes!

Keywords: metal, enzyme, cofactor, X-ray crystallography, PLP, porphyrin, cluster, catalyst, redox

Enzymes are said to be excellent catalysts that enable highly active and regio- and stereoselective transformations under mild conditions of normal temperature and pressure. However, what kinds of enzyme reactions can be realistically utilized? To effectively harness enzymes for targeted reactions, it is important to understand their characteristics from a molecular perspective. We are conducting research focused on understanding enzymes and enzyme reactions from a chemical viewpoint, as well as exploring the utilization of enzymes with non-natural substrates. In particular, we are creating new added value in "metalloenzymes" and "PLP enzymes," which are expected to be utilized due to their ability to perform complex reactions.

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Universal enzyme "Cleanerase AP-100PCW"

Universal enzyme "Cleanerase AP-100PCW"

Granular size of 20 to 50 mesh! Easy to mix with regular powdered detergent.

"Cleanerase AP-100PCW" is a granular general-purpose enzyme primarily composed of an alkali-resistant protease produced by Bacillus subtilis, developed for use in detergents. The product's features include excellent stability, particularly on the alkaline side, across a wide pH range, and it hydrolyzes insoluble and denatured proteins into soluble peptides and amino acids, making it suitable for cleaning protein-based stains and dirt adhered to fabrics. [Features] - Alkali-resistant protease as the main component - Granular form with a size of 20 to 50 mesh - Easy to mix with regular powdered detergents - Sturdy granules with minimal dusting - Easily soluble in water and stable against external denaturing factors *For more details, please refer to the PDF document or feel free to contact us.*

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Universal enzyme "Klinase AP-200L"

Universal enzyme "Klinase AP-200L"

It is primarily composed of refined high-unit alkaline protease and has a proven track record of numerous applications.

"Cleanerze AP-200L" is an alkaline-stable protease enzyme produced by Bacillus subtilis. Its greatest feature is its excellent heat resistance and particularly outstanding stability in alkaline conditions. Additionally, this product is primarily composed of purified high-activity alkaline protease and has a proven track record of numerous applications. [Features] ■ Works across a wide pH range of 6.0 to 11.0 ■ Excellent heat resistance ■ Outstanding stability in alkaline conditions *For more details, please refer to the PDF document or feel free to contact us.

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Universal enzyme "Krinase APSL-1311N"

Universal enzyme "Krinase APSL-1311N"

By combining three types of enzymes, the effect of breaking down and removing dirt, regardless of its type, is achieved.

The "Kurinase APSL-1311N" is a versatile enzyme that contains three types of enzymes: protease (protein-decomposing enzyme), amylase (starch-decomposing enzyme), and lipase (fat-decomposing enzyme). Dirt is made up of various components, but by incorporating these three types of enzymes—lipase for grease and oil, amylase for sticky substances like rice and polysaccharides found in ketchup, and protease for blood and meat juice stains—it effectively breaks down and removes all types of dirt. 【Features】 ■ Granular ■ Selected and blended enzymes with high activity in neutral to weak alkaline conditions *For more details, please refer to the PDF document or feel free to contact us.

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Standard PCR enzyme "Gene Taq NT"

Standard PCR enzyme "Gene Taq NT"

Test research reagents that can be used for standard PCR! Retains the same functionality as natural Taq DNA polymerase.

"Gene Taq NT" is a heat-stable DNA polymerase that is cloned from the DNA polymerase gene of Thermus aquaticus YT1, expressed in E. coli, and isolated and purified. It has the same function as the natural Taq DNA polymerase and can be used for standard PCR. Additionally, it possesses terminal transferase activity, allowing the resulting PCR products to be used for TA cloning. 【Features】 ■ Has the same function as natural Taq DNA polymerase ■ PCR products can be used for TA cloning ■ Possesses terminal transferase activity *For more details, please refer to the related links or feel free to contact us.

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Standard PCR enzyme "Gene Taq FP"

Standard PCR enzyme "Gene Taq FP"

Introducing test research reagents for RAPD PCR, which is greatly affected by contamination of genomic DNA!

The "Gene Taq FP" that we handle is a Taq DNA polymerase that has been purified to a higher degree using our unique technique, minimizing contamination from host bacterial genomic DNA. This product has the same functionality as Gene Taq, with a high amplification efficiency for DNA fragments of 1 kbp or less, and it features the absence of 5'→3' exonuclease activity. Additionally, it possesses terminal transferase activity, allowing the obtained PCR products to be used for TA cloning. 【Features】 ■ Further purified Gene Taq ■ Taq DNA polymerase with minimal contamination from host bacterial DNA ■ PCR products can be used for TA cloning *For more details, please refer to the related links or feel free to contact us.

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96-7 DNA polymerase for isothermal gene amplification technology LAMP method

96-7 DNA polymerase for isothermal gene amplification technology LAMP method

DNA polymerase 96-7 is an enzyme that can be used in the LAMP method. The LAMP method is a technique for rapidly amplifying and detecting target DNA or RNA.

This product is an enzyme that possesses 5'→3' DNA polymerase activity and strand displacement activity, capable of synthesizing new DNA strands while dissociating the hydrogen bonds of the double-stranded DNA template. The heat-stable strand-displacing DNA polymerase does not require the dissociation of double-stranded DNA due to its characteristics, allowing DNA synthesis at a constant temperature and making it resistant to synthesis inhibition caused by the secondary structure of DNA. **Features** - Has 5'→3' DNA polymerase activity and strand displacement activity - Enables DNA synthesis at a constant temperature - Suitable for synthesizing DNA strands with high GC content - Not affected by inhibition due to DNA secondary structures **Optimal Reaction Temperature** 50°C to 55°C **Inactivation Time** *1 70°C for 5 minutes *1 Inactivation temperature when the enzyme stock solution is directly heat-denatured **Applications** Applications utilizing strand displacement activity (such as isothermal gene amplification methods)

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Enzyme

Enzyme

We accept custom manufacturing of enzymes.

Currently, our company handles products from various countries of origin, including Japan, Europe, India, and China, and both the volume and variety of our offerings have been increasing year by year. Additionally, we have developed, improved, formulated, and manufactured our own products independently. Through stable supply of raw materials for domestic sales, exports, and imports, we believe we are able to contribute to your needs. We also offer small quantity responses and contract manufacturing, so please feel free to contact us.

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[Research Material] The Global Market for Genome Editing Technology

[Research Material] The Global Market for Genome Editing Technology

Global Market for Genome Editing Technologies: Zinc Finger Nucleases (ZFN), Transcription Activator-Like Effector Nucleases, Clustered Regularly Interspaced Short Palindromic Repeats ...

This research report (Global Genome Editing Techniques Market) investigates and analyzes the current state and future outlook of the global genome editing technology market over the next five years. It includes information on the overview of the global genome editing technology market, trends of major companies (sales, selling prices, market share), market size by segment, market size by major regions, and distribution channel analysis. The segments by type in the genome editing technology market include Zinc Finger Nucleases (ZFN), Transcription Activator-Like Effector Nucleases, Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR), and others. The segments by application focus on hospitals and laboratories. The regional segments are divided into North America, the United States, Europe, Asia-Pacific, Japan, China, India, South Korea, Southeast Asia, South America, the Middle East, and Africa to calculate the market size of genome editing technology. It also includes the market share of major companies in genome editing technology, product and business overviews, and sales performance.

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[Research Material] The Global Market for Restriction Enzymes

[Research Material] The Global Market for Restriction Enzymes

World Market for Restriction Enzymes: 5KU, 50KU, 500KU, 5000KU, Biopharmaceutical Companies, Academic/Research Institutions, Contract Research Organizations

This research report (Global Restriction Enzyme Market) investigates and analyzes the current state and future outlook of the global restriction enzyme market over the next five years. It includes information on the overview of the global restriction enzyme market, trends of major companies (sales, selling prices, market share), market size by segment, market size by major regions, and distribution channel analysis. The market segments by type focus on 5KU, 50KU, 500KU, and 5000KU, while the segments by application target biopharmaceutical companies, academic/research institutions, and contract research organizations. The regional segments are categorized into North America, the United States, Europe, Asia-Pacific, Japan, China, India, South Korea, Southeast Asia, South America, the Middle East, and Africa to calculate the market size of restriction enzymes. It also includes the market share of major companies in the restriction enzyme sector, product and business overviews, and sales performance.

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[Research Material] World Market for Biocatalysts

[Research Material] World Market for Biocatalysts

World Market for Biocatalysts: Hydrolytic Enzymes, Oxidoreductases, Transferases, Others, Food and Beverages, Cleaning Agents, Biofuel Production, Agriculture, and ...

This research report (Global Biocatalysis & Biocatalysts Market) investigates and analyzes the current state of the global biocatalyst market and its outlook for the next five years. It includes information on the overview of the global biocatalyst market, trends of major companies (sales, selling prices, market share), market size by segment, market size by major regions, and distribution channel analysis. The segments by type in the biocatalyst market include hydrolytic enzymes, oxidoreductases, transferases, and others, while the segments by application cover food and beverages, detergents, biofuel production, agriculture and feed, biopharmaceuticals, and others. The regional segments are categorized into North America, the United States, Europe, Asia-Pacific, Japan, China, India, South Korea, Southeast Asia, South America, the Middle East, and Africa, to calculate the market size of biocatalysts. It also includes the market share of major companies in the biocatalyst sector, product and business overviews, and sales performance.

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[Research Material] World Market for Liquid Bakery Enzymes

[Research Material] World Market for Liquid Bakery Enzymes

World Market for Liquid Bakery Enzymes: Bakery Protease Enzymes, Bakery Carbohydrase Enzymes, Bakery Lipase Enzymes, Cookies ...

This research report (Global Liquid Bakery Enzyme Market) investigates and analyzes the current state and outlook for the global liquid bakery enzyme market over the next five years. It includes information on the overview of the global liquid bakery enzyme market, trends of major companies (sales, selling prices, market share), market size by segment, market size by major regions, and distribution channel analysis. The segments by type in the liquid bakery enzyme market focus on bakery protease enzymes, bakery carbohydrase enzymes, and bakery lipase enzymes, while the segments by application target cookies & biscuits, cakes & pastries, and bread. The regional segments calculate the market size of liquid bakery enzymes by dividing them into North America, the United States, Europe, Asia-Pacific, Japan, China, India, South Korea, Southeast Asia, South America, the Middle East, and Africa. It also includes the market share of major companies in the liquid bakery enzyme sector, product and business overviews, and sales performance.

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[Market Report] Global Digestive Enzyme Market

[Market Report] Global Digestive Enzyme Market

The global digestive enzyme market is thriving and is expected to reach 1.6107 billion US dollars by 2031.

The global digestive enzyme market is poised for significant growth, with revenues expected to surge from approximately $760.24 million in 2022 to an estimated $1.6107 billion by 2031, reflecting a remarkable expansion during the forecast period from 2023 to 2031 at a rate of 8.7%. Digestive enzymes, which are essential proteins, play a crucial role in the human digestive system by helping to break down food substances such as proteins, fats, and carbohydrates into smaller, more easily absorbable molecules. This complex digestive process generates essential components like glycerol, amino acids, fatty acids, and monosaccharides, promoting efficient nutrient absorption and digestion within the body. For application methods, please check the [PDF download] button or apply directly through the related links.

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Proteins and Enzymes: Innovation and Development through Precision Fermentation

Proteins and Enzymes: Innovation and Development through Precision Fermentation

Recombinant bovine serum albumin (rBSA), bovine-derived DNase 1, thermolabile dsDNase 1, Taq DNA polymerase, and Brazein.

The current protein portfolio and technology of the Spanish company LEVPROT BIOSCIENCE are used in three major industries: food, IVD, and biopharmaceuticals. 【Brazain】 - A protein that is 1600 times sweeter than sugar - Provides the same sweetness with fewer calories consumed - Heat stability: can withstand low-temperature pasteurization 【Recombinant Bovine Serum Albumin (rBSA)】 - Contains no E. coli DNA - An ideal blocking solution for various immunoassays such as ELISA - Improved sensitivity with minimized non-specific binding - 20 to 100 times higher blocking efficiency than BSA 【Bovine-derived DNase 1 and Thermolabile dsDNase1】 - DNase I derived from Bos taurus (bovine) fermented in yeast: widely used for DNA removal and nucleic acid analysis in laboratories - Thermolabile dsDNase1 is inactivated by heat treatment (55°C) 【Taq DNA Polymerase】 - Contains no E. coli DNA - Contains no glycerol *For more details, please refer to the PDF document or feel free to contact us.

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Universal enzyme "Klinase SAP-200L"

Universal enzyme "Klinase SAP-200L"

I will introduce the alkaline-resistant protease enzyme produced by Bacillus subtilis.

The "Kurināze SAP-200L" is a versatile enzyme that works across a wide pH range of 6.0 to 12.0. This product is primarily composed of a purified high-activity alkaline protease, and its greatest feature is its superior heat resistance compared to conventional proteases, as well as its excellent stability over a wide pH range, particularly on the alkaline side. Additionally, it is a practical product that exhibits activity even in the presence of calcium chelators such as EDTA and tripolyphosphate. 【Features】 ■ Works across a wide pH range of 6.0 to 12.0 ■ Purified high-activity alkaline protease as the main component ■ Excellent heat resistance ■ Superior stability over a wide pH range, particularly on the alkaline side ■ Exhibits activity even in the presence of calcium chelators such as EDTA and tripolyphosphate *For more details, please refer to the PDF document or feel free to contact us.

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Enzyme 'Csa DNA Polymerase' for isothermal gene amplification technology LAMP method

Enzyme 'Csa DNA Polymerase' for isothermal gene amplification technology LAMP method

Csa DNA polymerase is an enzyme that can be used in the LAMP method. The LAMP method is a technique for amplifying and detecting target DNA or RNA in a short period of time.

This product is an enzyme that possesses 5’→ 3’ DNA polymerase activity and strand displacement activity, capable of synthesizing new DNA strands while dissociating the hydrogen bonds of the double-stranded DNA template. The heat-stable strand displacement type DNA polymerase does not require the dissociation of double-stranded DNA due to its characteristics, allowing DNA synthesis at a constant temperature, and it is not affected by synthesis inhibition caused by the secondary structure of DNA. 【Features】 ■ Has 5’→ 3’ DNA polymerase activity and strand displacement activity ■ Capable of DNA synthesis at a constant temperature ■ Suitable for synthesizing DNA strands with high GC content ■ Not inhibited by the secondary structure of DNA 【Optimal Reaction Temperature】 60°C to 70°C 【Inactivation Time】*1 85°C for 5 minutes *1 Inactivation temperature when the enzyme stock solution is directly heat-denatured 【Applications】 Applications utilizing strand displacement activity (such as isothermal gene amplification methods)

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Yeast Neutral Lactase 'GODO-YNL'

Yeast Neutral Lactase 'GODO-YNL'

Various applications using raw milk, skim milk powder (reconstituted milk), and whey as raw materials!

"GODO-YNL" is a yeast neutral lactase (lactose-decomposing enzyme) produced from yeast (Kluyveromyces lactis). It can be safely used as it is derived from microorganisms found in fermented dairy products such as cheese. It can hydrolyze the non-reducing terminal β-D-galactose residues of sugars that have β-D-galactoside bonds. 【Effects】 ■ Reduces stomach discomfort (lactose intolerance): Suitable for lactose-free dairy drinks and fermented dairy products. ■ Enhances sweetness: Suitable for sugar-free or low-sugar dairy drinks and fermented dairy products. ■ Prevents lactose crystallization: Suitable for smooth ice cream and milk jam. ■ Imparts caramel color (Maillard reaction): Suitable for aromatic milk coffee and milk jam. *For more details, please download the PDF or feel free to contact us.

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