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Basic Red 46 Basic Red 46. Group: Biochemicals. Alternative Names: 5-[ (e) -{4-[Benzyl (methyl) amino]phenyl}diazenyl]-1, 4-dimethyl-4, 5-dihydro-1h-1, 2, 4-triazol-1-ium bromide. Grades: Highly Purified. CAS No. 12221-69-1. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C18H23N6·Br. US Biological Life Sciences. USBiological 6
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BASIC RED 46 BASIC RED 46. Uses: Designed for use in research and industrial production. Additional or Alternative Names: C.I. BASIC RED 46. Appearance: Dark red powder. CAS No. 12221-69-1. Molecular formula: C18H21BrN6. Mole weight: 401.3. Product ID: ACM12221691. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry. 2
Acridine Orange Acridine Orange hydrochloride is the hydrocloride salt of Acridine Orange Stain, which is a cell and organelle membrane-permeable fluorescent dye that binds to nucleic acids and results in an altered spectral emission. It interacts with both DNA and RNA, emits green fluorescence when binds to DNA, and emits red fluorescence when binds to RNA. It is used in cell cycle and apoptosis studies and used as a lysosomal dye. It could distinguish cell death by apoptosis and necroptosis in human oligodendrocytes and mouse models. It is also used to analyze autophagy. Uses: A coloring agent. Synonyms: Acridine Orange hydrochloride;N,N,N',N'-Tetramethyl-3,6-acridinediamine hydrochloride; Rhoduline Orange; Acridine orange hydrochloride; Acridine Orange N; Acridine Orange Hydrochloride; 3,6-Acridinediamine, N3,N3,N6,N6-tetramethyl-, hydrochloride (1:1); 3,6-Acridinediamine, N,N,N',N'-tetramethyl-, monohydrochloride; Acridine Orange R; Acridine, 3,6-bis(dimethylamino)-, hydrochloride; Acridine, 3,6-bis(dimethylamino)-, monohydrochloride; 3,6-Bis(dimethylamino)acridine hydrochloride; Acridine Orange N; Acridine Orange NO; Acridine Orange NS; Basic Orange 14; Basic Orange 3RN; C.I. 46005; C.I. Basic Orange 14; Rhoduline Orange NO; Sumitomo Acridine Orange NO; Sumitomo Acridine Orange RK conc. Grades: ≥99% by HPLC. CAS No. 65-61-2. Molecular formula: C17H19N3.HCl. Mole weight: 301.81. BOC Sciences
Basic Red 1:1 Basic Red 1:1. Uses: Designed for use in research and industrial production. Additional or Alternative Names: BASIC RED;3,6-bis(ethylamino)-9-[2-(methoxycarbonyl)phenyl]-2,7-dimethyl-xanthyliuch;basicred1:1;Xanthylium,3,6-bis(ethylamino)-9-[2-(methoxycarbonyl)phenyl]-2,7-dimethyl-,chloride;3,6-bis(ethylamino)-9-[2-(methoxycarbonyl)phenyl]-2,7-dimethylxanthylium. Product Category: Basic Dyes. CAS No. 3068-39-1. Molecular formula: C27H29N2O3?Cl. Mole weight: 464.98. Density: g/cm³. Product ID: ACM3068391. Alfa Chemistry — ISO 9001:2015 Certified. Categories: Basic Red 18. Alfa Chemistry. 2
S-adenosylmethionine synthetase, Recombinant S-adenosylmethionine synthetase (EC 2.5.1.6) (also known as methionine adenosyltransferase (MAT)) is an enzyme that creates S-adenosylmethionine (AdoMet) by reacting methionine (a non-polar amino acid) and ATP (the basic currency of energy). AdoMet is a methyl donor for transmethylation. It gives away its methyl group and is also the propylamino donor in polyamine biosynthesis. S-adenosylmethionine synthetasecan be considered the rate-limiting step of the methionine cycle. S-adenosylmethionine (sam) is a methyl donor and allows dna methylation. once dna is methylated, it switches the genes off and therefore, s-adenosylmethionine can be considered tocontrol gene expressi...denosylmethioninesynthase isoform type-1; AdoMet synthase 1; MAT 1; Methionineadenosyltransferase I/III; MAT-I/III; MAT1A; AMS1. Enzyme Commission Number: EC 2.5.1.6. Purity: >90% (SDS-PAGE test). Mole weight: About 46kDa (SDS-PAGE detection). Activity: >700U/mg. Appearance: White powder, lyophilized. Storage: Redissolved in 30% glycerol, 4°C, store at -20°C/-80°C for long-term preservation, Avoid multiple freeze-thaw cycles. Form: Freeze dried powder. EC 2.5.1.6; MAT; MATA1; SAMS; SAMS1; Methionine adenosyltransferase 1; S-adenosylmethioninesynthase isoform type-1; AdoMet synthase 1; MAT 1; Methionineadenosyltransferase I/III; MAT-I/III; MAT1A; AMS1. Cat No: NATE-1151. Creative Enzymes

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