A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| Aminoallyl-UTP - ATTO-612Q | Aminoallyl-UTP - ATTO-612Q is a vital tool extensively used in the biomedical industry employed to label RNA for various applications including fluorescence in situ hybridization (FISH), real-time PCR and microarray analysis. This compound facilitates the detection and identification of RNA molecules involved in gene expression and contributes to the study of diseases such as cancer, neurodegenerative disorders and viral infections. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 612Q, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 612Q (free acid). Mole weight: 1211.22 (free acid). |  |
| Aminoallyl-UTP - ATTO-620 | Aminoallyl-UTP, a derivate of uridine triphosphate, stands as a proficient option for RNA detection assays. When paired with ATTO-620, it presents itself as an invaluable aid in visualizing and quantifying RNA, facilitating a more thorough domain for biomedical research. But alas, its potential doesn't stop there. Its medicinal application in the treatment of severe ailments, such as cancer and viral infections, only magnifies its already impressive nature. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 620, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 620 (free acid). Mole weight: 1032.22 (free acid). | |
| Aminoallyl-UTP - ATTO-633 | Aminoallyl-UTP is an indispensable compound employed for the purpose of labeling and analysis, playing a crucial role in RNA research by serving as a precursor. Through its utilization, the inclusion of aminoallyl groups into RNA molecules is made possible. By virtue of its conjugation with ATTO-633 dye is aminoallyl-UTP contributes to the enhancement of fluorescence detection, thereby facilitating the tracking and examination of RNA molecules. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 633, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 633 (free acid). Mole weight: 1072.22 (free acid). | |
| Aminoallyl-UTP - ATTO-647N | Aminoallyl-UTP is a nucleotide analog commonly used in biochemical and molecular biology research. It is utilized as a precursor for the synthesis of labeled RNA, allowing for specific tracking and analysis of RNA gene expression. Additionally, it has been employed in studies investigating the mechanism of RNA splicing and alternative splicing patterns. ATTO-647N is a fluorescent dye that can be conjugated to the aminoallyl-UTP for visualization and detection purposes. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 647N, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 647N (free acid). Mole weight: 1166.22 (free acid). | |
| Aminoallyl-UTP - ATTO-655 | Aminoallyl-UTP is an essential reagent in molecular biology for RNA labeling. It is used to synthesize aminoallyl-modified RNA that can be labeled with fluorescent dyes like ATTO-655 for microarray analysis, RNA FISH, and other imaging applications. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 655, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 655 (free acid). Mole weight: 1048.22 (free acid). | |
| Aminoallyl-UTP - ATTO-665 | Aminoallyl-UTP - ATTO-665 is a compound of biomedical research, emerging as a fluorescently labeled nucleotide. Its enzymatic integration into RNA during transcription paves the path to unveil the clandestine RNA molecules. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 665, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 665 (free acid). Mole weight: 1143.22 (free acid). | |
| Aminoallyl-UTP - ATTO-680 | | |
| Aminoallyl-UTP-ATTO-680 | Aminoallyl-UTP-ATTO-680 is recommended for direct enzymatic labeling of DNA/cDNA, such as PCR and Nick Translation. It was incorporated as an alternative to its natural counterpart, dTTP. The resulting dye-labeled DNA/cDNA probes are ideal for fluorescent hybridization applications such as FISH or microarray-based gene expression profiling. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 680, Triethylammonium salt. Grades: ≥95% by HPLC. Molecular formula: C39H49N6O20P3S (free acid). Mole weight: 1046.82 (free acid). | |
| Aminoallyl-UTP - ATTO-700 | Aminoallyl-UTP, a compound indispensably used in biomedical industries, is a notable reagent used for constructing aminoallyl-modified RNA for specific gene expression analysis. Its incomparable role in identifying RNA expression patterns and studying gene regulatory mechanisms makes it a critical tool in the scientific community. ATTO-700 labeled Aminoallyl-UTP, a variant of this compound, is a popular choice for real-time PCR and microarray analysis, especially in the area of cancer research and diagnosis. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 700, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 700 (free acid). Mole weight: 1086.22 (free acid). | |
| Aminoallyl-UTP - ATTO-740 | Aminoallyl-UTP - ATTO-740 is an indispensable compound serving as a fluorescent nucleotide analog. It facilitates the annotation of RNA while cDNA is synthesized. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 740, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 740 (free acid). Mole weight: 988.22 (free acid). | |
| Aminoallyl-UTP - ATTO-MB2 | Aminoallyl-UTP, a modified nucleotide employed in biomedical research for RNA transcript labeling, acts as a vital constituent of the "Amino Allyl MessageAmp II RNA Amplification Kit". Utilized in the amplification of RNA from minute samples, it facilitates distinct downstream applications which include gene expression profiling and disease biomarker identification. ATTO-MB2 - a variant of Aminoallyl-UTP suffused with a fluorescent tag - facilitates visualization of RNA labeling and detection. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO-MB2, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C31H39N6O16P3S (free acid). Mole weight: 876.66 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho101 | Aminoallyl-UTP is an essential recompound. It is utilized for the enzymatic labeling of RNA molecules with aminoallyl moieties. This labeled RNA can then be further conjugated with fluorescent dyes like ATTO-Rho101 for applications such as in vitro diagnostics, gene expression analysis and tracking RNA localization within cells. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho101, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C49H57N6O18P3 (free acid). Mole weight: 1110.29 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho11 | Aminoallyl-UTP, a highly-valued nucleotide analog in molecular biology, serves as a crucial tool for both RNA labeling and purification. By facilitating incorporation into RNA through in vitro transcription, it enables highly-sensitive fluorescent labeling with dyes such as ATTO-Rho11. Such versatility permits unexpected benefits for gene expression profiling, mRNA localization, and splicing site analysis. Its usage markedly opens new vistas in the exploration of RNA function. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho11, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C47H57N6O18P3 (free acid). Mole weight: 1086.29 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho12 | Aminoallyl-UTP, a modified nucleotide, serves as a substrate for in vitro transcription to enable RNA probe synthesis. Effective in its role as a label substrate, Aminoallyl-UTP effectively pairs and fluoresces with dyes like ATTO-Rho12 within the context of in situ hybridization and microscopy. For its varied applications, such as RNA labeling in quantitative PCR or microarray analysis, Aminoallyl-UTP remains adaptable and multifaceted in its role within biochemical research. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho12, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C53H69N6O18P3 (free acid). Mole weight: 1170.39 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho13 | Aminoallyl-UTP, a structurally modified nucleotide harboring the potential to be integrated into RNA for the ultimate objective of tagging and disclosure of the sequence data, stands out as an indispensable tool in the scientific arena specializing in the biomedical research domain. Its applications and implications in the field of mRNA labeling, microarray analysis and RNA sequencing exhibits its noteworthy significance in comprehending the genetics and epigenetics of an organism. Its proven utility in elucidating the mechanisms underlying several complex maladies such as cancer and neurological disorders stands as a powerful testament to its potential to unravel the intricate mysteries of cell differentiation and gene expression. Its synergistic binding with the fluorescent dye, ATTO-Rho13, empowers the scientific community to gain live imaging insights into the manifestation of RNA expression across healthy and stressed cells and tissues. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho13, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C53H65N6O18P3 (free acid). Mole weight: 1166.37 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho14 | Aminoallyl-UTP, the wondrous nucleotide analog indispensable in bioassays, faithfully marks RNA molecules when used in tandem with enzymes or fluorescent dyes - think ATTO-Rho14. Yet an even brighter future awaits: potential applications as an antiviral agent against respiratory syncytial virus (RSV). Be dazzled by its versatility! Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho14, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C53H61Cl4N6O18P3 (free acid). Mole weight: 1302.20 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho6G | Aminoallyl-UTP - ATTO-Rho6G is an essential tool with remarkable significance within the realm of biomolecular investigation assuming a pivotal role in RNA labeling and crosslinking endeavors. The seamless combination with ATTO-Rho6G dye bestows upon it the power to effortlessly detect and monitor labeled RNA molecules. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho6G, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C43H53N6O18P3 (free acid). Mole weight: 1034.26 (free acid). | |
| Aminoallyl-UTP - ATTO-Thio12 | Aminoallyl-UTP - ATTO-Thio12 is emerging as a modified nucleotide of paramount importance when it comes to RNA labeling and research and development. Its unrivaled ability to functionalize RNA molecules paves the way for diverse applications, ranging from microarray analysis to fluorescence imaging. By successfully conjugating ATTO-Thio12 is a profoundly thiol-reactive fluorescent dye, with aminoallyl-UTP labeled RNA, groundbreaking advancements in gene expression profiling and molecular imaging can be achieved. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Thio12, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C41H49N6O17P3S (free acid). Mole weight: 1022.84 (free acid). | |
| Aminoallyl-UTP - Cy3 | Aminoallyl-UTP - Cy3 is a valuable tool in the biomedical industry used for fluorescent labeling of RNA enabling efficient incorporation of the modified nucleotide into RNA during transcription. Coupled with the Cy3 dye, it allows for precise detection and visualization of RNA in various research applications, including gene expression analysis, RNA quantification and mRNA localization studies. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Cy3, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C43H56N5O22P3S2 (free acid). Mole weight: 1151.97 (free acid). | |
| Aminoallyl-UTP - Cy5 | Aminoallyl-UTP - Cy5 is a highly fluorescent probe used in biomedical research for labeling RNA molecules. Aminoallyl-UTP incorporates into RNA during transcription and is subsequently labeled with Cy5 dye via a reactive amino group. This labeled RNA is ideal for fluorescence in situ hybridization (FISH) assays and microarray analysis to study gene expression, RNA localization and dynamics in various diseases and biological processes. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Cy5, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C45H58N5O22P3S2 (free acid). Mole weight: 1178.01 (free acid). | |
| Aminoallyl-UTP - DY-480XL | Aminoallyl-UTP - DY-480XL, a novel nucleotide, holds significance for the biomedicine industry as it serves as a crucial molecule for RNA labeling and detection. It plays a vital role in synthesizing fluorescently labeled RNA that not only assists in scrutinizing RNA expression levels but also sheds light on RNA localization. With its potential for investigating RNA-protein interactions and identifying RNA viruses and diseases, including cancer, Aminoallyl-UTP - DY-480XL is an invaluable asset for researchers and clinicians alike. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DY 480XL, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C38H48N5O21P3S (free acid). Mole weight: 1035.80 (free acid). | |
| Aminoallyl-UTP - DY-485XL | Aminoallyl-UTP is a modified form of uridine triphosphate that contains an amine and an allyl group. This product can be used as a substrate for RNA polymerase in an in vitro transcription reaction with incorporation into RNA. It is commonly used in the labeling of RNA for microarray analysis and RNA sequencing, as well as for site-specific RNA-protein crosslinking studies. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DY 485XL, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C37H48N5O21P3S (free acid). Mole weight: 1023.79 (free acid). | |
| Aminoallyl-UTP - DY-751 | Aminoallyl-UTP, a nucleotide that has undergone modification, is an instrumental component of RNA labeling and detection in biomedicine. It is capable of being integrated into RNA transcripts via in vitro transcription, leading to its labeling with fluorescent dye, which can then be utilized for imaging or detection through hybridization. Utilized in the detection of gene expression and the examination of mRNA localization, as well as the identification of RNA-protein interactions, Aminoallyl-UTP has been studied in various diseases, such as cancer and neurological disorders. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DY 751, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C54H70N5O23P3S2 (free acid). Mole weight: 1313.31 (free acid). | |
| Aminoallyl-UTP - DY-776 | Aminoallyl-UTP - DY-776 is an indispensable compound utilized in compound applications functioning as a modified ribonucleoside triphosphate. It assumes a critical role in labeling and detecting RNA molecules within diverse biological investigations. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DY 776, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C56H66N5O23P3S2 (free acid). Mole weight: 1334.20 (free acid). | |
| Aminoallyl-UTP - DYQ-660 | Aminoallyl-UTP, a modified nucleotide renowned for its efficiency, optimizes RNA labeling in biomedical contexts. Often utilized in microarray and fluorescence in situ hybridization (FISH), this operationalized compound enhances the yields of fluorescent dyes through its advantageous incorporation profile. With relatively reduced toxicity when compared to peer alternatives, Aminoallyl-UTP represents a highly sought after innovation in biochemical processing. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DYQ 660, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C51H62N5O20P3S (free acid). Mole weight: 1190.05 (free acid). | |
| Aminoallyl-UTP - DYQ-661 | Aminoallyl-UTP, a potent and versatile chemical reagent in the realm of biomedical research, is employed in the detection and labeling of RNA molecules. It plays a pivotal role in the analysis of microarrays and the synthesis of cDNA libraries. When used in tandem with reverse transcriptase, it is highly efficacious in labeling RNA for the purposes of Northern blotting and in situ hybridization assays. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DYQ 661, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C51H61N5O23P3S2 (Anion). Mole weight: 1269.10 (Anion). | |
| Aminoallyl-UTP - MANT | Aminoallyl-UTP, a potent product having niche importance in the biomedical industry, is used for RNA molecules synthesis, particularly to introduce aminoallyl-uridine residues to facilitate expression analysis and labeling. The remarkable potential of this molecular tool lies in its ability to help researchers gain a deeper understanding of gene expression profiles, which hold the key to unraveling complex mechanisms of diseases like Alzheimers, Parkinsons, and cancer. This has led to its wide adoption in the pharmaceutical industry for drug discovery and development. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with MANT, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C20H27N4O16P3 (free acid). Mole weight: 672.37 (free acid). | |
| Aminoallyl-UTP - OYSTER-656 | Aminoallyl-UTP is a crucial recompound widely utilized for labeling RNA during enzymatic transcription reactions. This labeled RNA plays a vital role in various applications such as microarray analysis, RNA sequencing and in situ hybridization techniques. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with OYSTER 656, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- OYSTER 656 (free acid). Mole weight: 1255.19 (free acid). | |
| Aminoallyl-UTP - solution | Aminoallyl-UTP solution is an indispensable element, finding utility in generating intricate RNA compositions. Serving as a prevalent tool across multifaceted domains, encompassing gene expression analysis, RNA sequencing and the exploration of RNA-protein interplay, this compound embodies paramount significance. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 112131-73-4. Molecular formula: C12H20N3O15P3 (free acid). Mole weight: 539.22 (free acid). | |
| Aminoallyl-UTP - Texas Red | Aminoallyl-UTP - Texas Red is a chemical entity that has been purposefully engineered and altered to allow for highly refined and exacting labeling of RNA via intricate enzymatic processes, offering unique and novel solutions to pressing scientific challenges. This multifaceted and versatile compound has been at the forefront of evocative fluorescent labeling techniques, imbuing RNA microarray analysis and in situ hybridization with incredible depth and power. Moreover, the readily detectable Texas Red molecule appended to the amino group of Aminoallyl-UTP allows for stunningly clear imaging of labeled RNA in an unparalleled variety of biological test-beds, thereby opening up new avenues of investigation and discovery into the fundamental processes of gene expression and regulation. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Texas Red, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C49H59N6O22P3S2 (free acid). Mole weight: 1241.10 (free acid). | |
| Aminoallyl-UTP-X - Cy3 | Aminoallyl-UTP-X - Cy3 is a dazzlingly vibrant fluorescent dye, predominantly finding its purpose in the intricate art of RNA sequence labeling. Its presence pervades the abyss of scientific techniques, particularly microarray analysand the enigmatic fluorescence in situ hybridization (FISH). The magnificent capabilities of Aminoallyl-UTP-X - Cy3 are harnessed to exemplify the visual manifestation and meticulous quantification of remarkable RNA molecules. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Cy3, Triethylammonium salt; UTP-X-Cy3, UTP-17-Cy3, Cy3-17-UTP. Grades: ≥ 95% by HPLC. Molecular formula: C49H67N6O23P3S2 (free acid). Mole weight: 1165.13 (free acid). | |
| Aminoallyl-UTP-X - Cy5 | Aminoallyl-UTP-X - Cy5, a highly specialized reagent, has found wide-spread use in the domain of biomedicine as an efficient tool for detection and labeling procedures. With the ability to introduce several labels such as Alexa Fluor 647, Biotin, Cy3, Cy5.5, Cy7, Digoxigenin, and Rhodamine Red into RNA via in vitro transcription, Aminoallyl-UTP-X - Cy5 plays a pivotal role in DNA-microarrays, primed in-situ labeling (PRINS), and reverse transcription-polymerase chain reaction (RT-PCR). Its applicability is vast, ranging from research fields of cancer biology to neurobiology, and immunology. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Cy5, Triethylammonium salt; UTP-X-Cy5, UTP-17-Cy5, Cy5-17-UTP. Grades: ≥ 95% by HPLC. Molecular formula: C51H69N6O23P3S2 (free acid). Mole weight: 1291.17 (free acid). | |
| aminoazanium | aminoazanium. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Hydrazinium. Product Category: Heterocyclic Organic Compound. CAS No. 18500-32-8. Molecular formula: H5N2+. Mole weight: 33.0531 g/mol. Purity: 0.96. IUPACName: aminoazanium. Product ID: ACM18500328. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Amino-BChept-5-ene-COOH HCl(R,R,S,S/S,S,R,R) | Synonyms: (1R,2R,3S,4S/1S,2S,3R,4R)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxylic acid hydrochloride. CAS No. 53623-52-2. Molecular formula: C8H11NO2·HCl. Mole weight: 189.64. | |
| Amino-BChept-5-ene-COOH(R,R,S,S/S,S,R,R) | Synonyms: (1R,2R,3S,4S/1S,2S,3R,4R)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxylic acid. Molecular formula: C8H11NO2. Mole weight: 153.18. | |
| Amino-BCheptane-COOH HCl(S,R,S,R/R,S,R,S) | Synonyms: (1S,2R,3S,4R/1R,2S,3R,4S)-3-aminobicyclo[2.2.1]heptane-2-carboxylic acid hydrochloride (1:1); (CIS)-2-AMINO-3-CARBOXYBICYCLO[2.2.1]HEPTANE HYDROCHLORIDE. CAS No. 14932-25-3. Molecular formula: C8H13NO2HCl. Mole weight: 191.66. | |
| Amino-BCheptane-COOH(S,R,S,R/R,S,R,S) | Synonyms: (1S,2R,3S,4R/1R,2S,3R,4S)-3-aminobicyclo[2.2.1]heptane-2-carboxylic acid; 3-Amino-bicyclo[2.2.1]heptane-2-carboxylic acid; 3-Amino-2-norbornanecarboxylic acid. Grades: ≥ 95%. CAS No. 76198-36-2. Molecular formula: C8H13NO2. Mole weight: 155.19. | |
| aminobenzoate decarboxylase | A pyridoxal-phosphate protein. Group: Enzymes. Enzyme Commission Number: EC 4.1.1.24. CAS No. 9024-73-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4769; aminobenzoate decarboxylase; EC 4.1.1.24; 9024-73-1. Cat No: EXWM-4769. |  |
| Aminobenzoate potassium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Aminobenzoate Potassium | Aminobenzoate Potassium is an FDA approved medication used in the protection of mammals from glucose toxicity. Widely distributed in nature as a B complex factor. BakerÂs yeast contains 5 to 6 ppm, brewerÂs yeast from 10 to 100 ppm. Group: Biochemicals. Grades: Highly Purified. CAS No. 138-84-1. Pack Sizes: 1g, 5g. Molecular Formula: C7H6KNO2, Molecular Weight: 175.23. US Biological Life Sciences. |  Worldwide |
| Aminobenzoate sodium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Aminobenzoic acid | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Aminobenzoic Acid, USP | P-aminobenzoic acid appears as colorless crystals that discolor on exposure to light and air. (NTP, 1992);Solid. Group: Liquid crystal (lc) building blocks. CAS No. 150-13-0. Product ID: 4-aminobenzoic acid. Molecular formula: 137.14g/mol. Mole weight: C7H7NO2;C7H7NO2. C1=CC(=CC=C1C(=O)O)N. InChI=1S/C7H7NO2/c8-6-3-1-5 (2-4-6)7 (9)10/h1-4H, 8H2, (H, 9, 10). ALYNCZNDIQEVRV-UHFFFAOYSA-N. |  |
| Aminobenztropine | solid. Group: Fluorescence/luminescence spectroscopy. | |
| Aminobenzyl Alcohol | Aminobenzyl Alcohol. Group: Polymers. Product ID: amino(phenyl)methanol. Molecular formula: 123.15g/mol. Mole weight: C7H9NO. C1=CC=C(C=C1)C(N)O. InChI=1S/C7H9NO/c8-7 (9)6-4-2-1-3-5-6/h1-5, 7, 9H, 8H2. QTQUJRIHTSIVOF-UHFFFAOYSA-N. | |
| Amino Blue Polystyrene Particles Crosslinked | Amino Blue Polystyrene Particles Crosslinked. Group: Polystyrene (ps). | |
| Aminobutanol | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Aminobutanol | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmacopeia & metrological institutes standards. | |
| Aminobutyl-DOTA-tris(t-butyl ester) | Aminobutyl-DOTA-tris(t-butyl ester) is a bifunctional chelating agent. Synonyms: Tri-tert-butyl 2,2',2''-(10-(2-((4-aminobutyl)amino)-2-oxoethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate; 1,4,7,10-Tetraazacyclododecane-1,4,7-tris(t-butyl acetate)-10-(4-aminobutyl)acetamide. CAS No. 1402393-59-2. Molecular formula: C32H62N6O7. Mole weight: 642.87. | |
| aminobutyraldehyde dehydrogenase | The enzyme from some species exhibits broad substrate specificity and has a marked preference for straight-chain aldehydes (up to 7 carbon atoms) as substrates. The plant enzyme also acts on 4-guanidinobutanal (cf. EC 1.2.1.54 γ-guanidinobutyraldehyde dehydrogenase). As 1-pyrroline and 4-aminobutanal are in equilibrium and can be interconverted spontaneously, 1-pyrroline may act as the starting substrate. The enzyme forms part of the arginine-catabolism pathway and belongs in the aldehyde dehydrogenase superfamily. Group: Enzymes. Synonyms: γ-guanidinobutyraldehyde dehydrogenase (ambiguous); ABAL dehydrogenase; 4-aminobutyraldehyde dehydrogenase; 4-aminobutanal dehydrogenase; γ-aminobutyraldehyde dehydroganase; 1-pyrroline dehydrogenase; ABALDH; YdcW. Enzyme Commission Number: EC 1.2.1.19. CAS No. 9028-98-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1124; aminobutyraldehyde dehydrogenase; EC 1.2.1.19; 9028-98-2; γ-guanidinobutyraldehyde dehydrogenase (ambiguous); ABAL dehydrogenase; 4-aminobutyraldehyde dehydrogenase; 4-aminobutanal dehydrogenase; γ-aminobutyraldehyde dehydroganase; 1-pyrroline dehydrogenase; ABALDH; YdcW. Cat No: EXWM-1124. | |
| Aminocaproic acid | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmacopeia & metrological institutes standards. | |
| Aminocaproic acid | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: CL 10304, Acepramine, Amikar, omega-Aminohexanoic acid, NSC 26154,Aminocaproic Acid, Acepramin, epsilon-Leucine, Ï-Aminocaproic acid, Aminokapron, Ipsilon, 177 J.D., Epsicapron, Epsilon S, Hepin, NSC 400230, Caplamin, Caprocid, Afibrin, omega-Aminocaproic acid, epsilon-Aminocaproic acid, 6-Aminohexanoic acid, Caprolisin, NSC 212532, Epsilcapramin, Respramin, Acikaprin, EACS, ACS, Epsamon, Hemocaprol, epsilon-Amino-n-hexanoic acid, 6-Amino-n-hexanoic acid, EACA, Capramol, Epsikapron, epsilon-Aminohexanoic acid, Amicar, 6-Aminocaproic acid, Hemopar, Ï-Aminohexanoic acid, CY 116, epsilon-Norleucine. | |
| Aminocaproic Nitrilotriacetic Acid (AC-NTA) | A metal chelating agent. Group: Biochemicals. Alternative Names: AC-NTA. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Aminocaproic Nitrilotriacetic Acid Tri-tert-butylester | A metal chelating agent. Group: Biochemicals. Alternative Names: N6-(6-Amino-1-oxohexyl)-N2,N2-bis[2-(1,1-dimethylethoxy)-2-oxoethyl]-L-lysine 1,1-Dimethylethyl Ester. Grades: Highly Purified. CAS No. 1218921-96-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Aminocarb | Aminocarb is a carbamate insecticide. Group: Biochemicals. Grades: Highly Purified. CAS No. 2032-59-9. Pack Sizes: 50mg, 100mg. Molecular Formula: C11H16N2O2, Molecular Weight: 208.26. US Biological Life Sciences. | Worldwide |
| aminocarboxymuconate-semialdehyde decarboxylase | Product rearranges non-enzymically to picolinate. Group: Enzymes. Synonyms: picolinic acid carboxylase; picolinic acid decarboxylase; α-amino-β-carboxymuconate-ε-semialdehade decarboxylase; α-amino-β-carboxymuconate-ε-semialdehyde β-decarboxylase; 2-amino-3-(3-oxoprop-2-enyl)but-2-enedioate carboxy-lyase; 2-amino-3-(3-oxoprop-1-en-1-yl)but-2-enedioate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.45. CAS No. 37289-47-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4790; aminocarboxymuconate-semialdehyde decarboxylase; EC 4.1.1.45; 37289-47-7; picolinic acid carboxylase; picolinic acid decarboxylase; α-amino-β-carboxymuconate-ε-semialdehade decarboxylase; α-amino-β-carboxymuconate-ε-semialdehyde β-decarboxylase; 2-amino-3-(3-oxoprop-2-enyl)but-2-enedioate carboxy-lyase; 2-amino-3-(3-oxoprop-1-en-1-yl)but-2-enedioate carboxy-lyase. Cat No: EXWM-4790. | |
| Aminocardiolipin | Amino-CL can be modified with or attached to amine reactive probes/surfaces. Cardiolipin (CL) is an important component in prokaryotic and in eukaryotic inner mitochondrial membranes. Monolysocardiolipin is an intermediate in CL remodeling, and acetyl transferase tafazzin mutations impairing linoleic acid transfer to MCL are considered the main reason of Barth syndrome. Synonyms: Amino-CL. Molecular formula: C69H135NO17P2. Mole weight: 1312.78. | |
| Aminocarpoic Acid | Aminocarpoic Acid. CAS No. 60-32-2. |  CA, FL & NJ |
| Aminocatechol | A phenol derivative with inhibitory activity against matrix metalloproteinase (MMP). Group: Biochemicals. Alternative Names: 4-Aminopyrocatechol; 1-Amino-3,4-dihydroxybenzene; 3,4-Dihydroxyaniline; 3,4-Dihydroxyphenylamine; 4-Amino-1,2-benzenediol; 4-Aminocatechol; A 3253; KYJ 3-018. Grades: Highly Purified. CAS No. 13047-04-6. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Aminochloropentenedioic acid | It is produced by the strain of Streptomyces viridogenes MA5450. It has the activity of resisting gambogic micrococcus. Synonyms: [R-(Z)]-4-Amino-3-chloro-2-pentenedioic acid; 3-Acpa; 2-Amino-3-chloro-3-pentenedioic; 4-Amino-3-chloro-2-pentenedioic acid; 2-Pentenedioic acid, 4-amino-3-chloro-, (R-(Z))-. CAS No. 90288-29-2. Molecular formula: C5H6ClNO4. Mole weight: 179.56. | |
| Aminocoumarin dextran | Fluorescein a-cyclodextrin. Product ID: 9-01398. Mole weight: Mw 40,000. |  |
| Aminocoumarin heparin | a-amylase substrate for colorimetric assay. Product ID: 9-01088. Mole weight: Av. Mw ~15,000. Purity: ~5 mol% Dansyl. | |
| Aminocoumarin pectin | Dextran labeled with fluorescein isothiocyanate. Product ID: 9-01093. Purity: ~5 mol%. Reference: Experientia, 23, 805, 1967. | |
| Aminocoumarin pullulan | . dextran labeled with fluorescein isothiocyanate. Product ID: 9-01094. Purity: dye content ~5-7 mol%. | |
| aminocyclopropanecarboxylate oxidase | A nonheme iron enzyme. Requires CO2 for activity. In the enzyme from plants, the ethylene has signalling functions such as stimulation of fruit-ripening. Group: Enzymes. Synonyms: ACC oxidase; ethylene-forming enzyme. Enzyme Commission Number: EC 1.14.17.4. CAS No. 98668-53-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0962; aminocyclopropanecarboxylate oxidase; EC 1.14.17.4; 98668-53-2; ACC oxidase; ethylene-forming enzyme. Cat No: EXWM-0962. | |
| aminodeoxychorismate lyase | A pyridoxal-phosphate protein. Forms part of the folate biosynthesis pathway. Acts on 4-amino-4-deoxychorismate, the product of EC 2.6.1.85, aminodeoxychorismate synthase, to form p-aminobenzoate. Group: Enzymes. Synonyms: enzyme X; 4-amino-4-deoxychorismate lyase; 4-amino-4-deoxychorismate pyruvate-lyase. Enzyme Commission Number: EC 4.1.3.38. CAS No. 132264-33-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4914; aminodeoxychorismate lyase; EC 4.1.3.38; 132264-33-6; enzyme X; 4-amino-4-deoxychorismate lyase; 4-amino-4-deoxychorismate pyruvate-lyase. Cat No: EXWM-4914. | |
| aminodeoxychorismate synthase | The enzyme is composed of two parts, PabA and PabB. In the absence of PabA and glutamine, PabB converts ammonia and chorismate into 4-amino-4-deoxychorismate (in the presence of Mg2+). PabA converts glutamine into glutamate only in the presence of stoichiometric amounts of PabB. This enzyme is coupled with EC 4.1.3.38, aminodeoxychorismate lyase, to form 4-aminobenzoate. Group: Enzymes. Synonyms: ADC synthase; 4-amino-4-deoxychorismate synthase; PabB; chorismate:L-glutamine amido-ligase (incorrect). Enzyme Commission Number: EC 2.6.1.85. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2926; aminodeoxychorismate synthase; EC 2.6.1.85; ADC synthase; 4-amino-4-deoxychorismate synthase; PabB; chorismate:L-glutamine amido-ligase (incorrect). Cat No: EXWM-2926. | |
| aminodeoxyfutalosine deaminase | The enzyme, found in several bacterial species, is part of the futalosine pathway for menaquinone biosynthesis. Group: Enzymes. Synonyms: AFL deaminase; aminofutalosine deaminase; mqnX (gene name). Enzyme Commission Number: EC 3.5.4.40. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4569; aminodeoxyfutalosine deaminase; EC 3.5.4.40; AFL deaminase; aminofutalosine deaminase; mqnX (gene name). Cat No: EXWM-4569. | |
| aminodeoxyfutalosine nucleosidase | The enzyme, found in several bacterial species, catalyses a step in a modified futalosine pathway for menaquinone biosynthesis. While the enzyme from some organisms also has the activity of EC 3.2.2.9, adenosylhomocysteine nucleosidase, the enzyme from Chlamydia trachomatis is specific for 6-amino-6-deoxyfutalosine. Group: Enzymes. Synonyms: AFL nucleosidase; aminofutalosine nucleosidase; methylthioadenosine nucleosidase; MqnB. Enzyme Commission Number: EC 3.2.2.30. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3985; aminodeoxyfutalosine nucleosidase; EC 3.2.2.30; AFL nucleosidase; aminofutalosine nucleosidase; methylthioadenosine nucleosidase; MqnB. Cat No: EXWM-3985. | |
| aminodeoxyfutalosine synthase | This enzyme is a member of the 'AdoMet radical' (radical SAM) family. S-Adenosyl-L-methionine acts as both a radical generator and as the source of the transferred adenosyl group. The enzyme, found in several bacterial species, is part of the futalosine pathway for menaquinone biosynthesis. Group: Enzymes. Synonyms: MqnE; AFL synthase; aminofutalosine synthase; S-adenosyl-L-methionine:3-[(1-carboxyvinyl)-oxy]benzoate adenosyltransferase (bicarbonate-hydrolysing, 6-amino-6-deoxyfutalosine-forming). Enzyme Commission Number: EC 2.5.1.120. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2736; aminodeoxyfutalosine synthase; EC 2.5.1.120; MqnE; AFL synthase; aminofutalosine synthase; S-adenosyl-L-methionine:3-[(1-carboxyvinyl)-oxy]benzoate adenosyltransferase (bicarbonate-hydrolysing, 6-amino-6-deoxyfutalosine-forming). Cat No: EXWM-2736. | |
Our database is helping our users find suppliers everyday.
