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Reference: BLA-1X
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Blasticidin S is used as a selection antibiotic that inhibits protein synthesis in bacteria and eukaryotes. Transformed cells containing the resistance genes bls, bsr, or BSD can be selected.
Reference: BLA-5X
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Blasticidin S is used as a selection antibiotic that inhibits protein synthesis in bacteria and eukaryotes. Transformed cells containing the resistance genes bls, bsr, or BSD can be selected.
Reference: G418-B
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G-418 Solution is used as a selection antibiotic in cell culture. It blocks polypeptide synthesis. Transformed cells containing the neomycin resistance genes neo can be selected.
Reference: G418-H
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G-418 Solution is used as a selection antibiotic in cell culture. It blocks polypeptide synthesis. Transformed cells containing the neomycin resistance genes neo can be selected.
Reference: G418-Q
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G-418 is used as a selection antibiotic in cell culture. It blocks polypeptide synthesis. Transformed cells containing the neomycin resistance genes neo can be selected.
Reference: G418-R
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G-418 is used as a selection antibiotic in cell culture. It blocks polypeptide synthesis. Transformed cells containing the neomycin resistance genes neo can be selected.
Reference: HYG-H
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Hygromycin B solution is a selection antibiotic that inhibits protein synthesis in prokaryotes and eukaryotes. Transformed cells containing the hygromycin resistance gene (hyg or hph) can be selected.
Reference: PUR-1X
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Puromycin is a selection antibiotic that inhibits protein synthesis in prokaryotes and eukaryotes. Transformed cells containing the puromycin N-acetyl-transferase gene (pac) can be selected.
Reference: 4K-1000
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FuGENE® 4K is our newest and most advanced, 100% synthetic, multi-component transfection reagent designed for the delivery of DNA into both challenging and routine mammalian cell lines. FuGENE® 4K was developed to...
Reference: 21576-10
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A bicyclic monoterpene with diverse biological activities; reduces the growth of a panel of seven Gram-positive bacteria, seven Gram-negative bacteria, and eight yeast strains (MICs = 0.75-1.29, 1.05-1.59, and...
Reference: 4K-5000
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FuGENE® 4K is our newest and most advanced, 100% synthetic, multi-component transfection reagent designed for the delivery of DNA into both challenging and routine mammalian cell lines. FuGENE® 4K was developed to...
Reference: 21576-50
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A bicyclic monoterpene with diverse biological activities; reduces the growth of a panel of seven Gram-positive bacteria, seven Gram-negative bacteria, and eight yeast strains (MICs = 0.75-1.29, 1.05-1.59, and...
Reference: HD-1000
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FuGENE® HD is a 100% synthetic, multi-component, non-liposomal transfection reagent designed for the delivery of DNA into more challenging eukaryotic and insect cell lines. FuGENE® HD interacts with nucleic acids &...
Reference: 21719-1
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A monocyclic monoterpene with diverse biological activities; inhibits the growth of bacteria including S. aureus, B. cereus, E. faecalis, E. coli, P. aeruginosa, K. pneumoniae, M. catarrhalis, and C. neoformans (MICs...
Reference: HD-5000
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FuGENE® HD is a 100% synthetic, multi-component, non-liposomal transfection reagent designed for the delivery of DNA into more challenging eukaryotic and insect cell lines. FuGENE® HD interacts with nucleic acids &...
Reference: 21719-5
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A monocyclic monoterpene with diverse biological activities; inhibits the growth of bacteria including S. aureus, B. cereus, E. faecalis, E. coli, P. aeruginosa, K. pneumoniae, M. catarrhalis, and C. neoformans (MICs...
Reference: F6-1000
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FuGENE® 6 is a multi-component lipid-based transfection reagent that allows for the efficient delivery of all sizes of DNA into a broad range of cell types with extremely low cytotoxicity. FuGENE® 6 saves time and...
Reference: 22184-1
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A monoterpene with diverse biological activities; reduces compound action potential (CAP) peak amplitude in isolated frog sciatic nerves (IC50 = 0.51 mM); inhibits the radial growth of M. gypsum, T. vercossum, and C....
Reference: F6-5000
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FuGENE® 6 is a multi-component lipid-based transfection reagent that allows for the efficient delivery of all sizes of DNA into a broad range of cell types with extremely low cytotoxicity. FuGENE® 6 saves time and...
Reference: 22184-10
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A monoterpene with diverse biological activities; reduces compound action potential (CAP) peak amplitude in isolated frog sciatic nerves (IC50 = 0.51 mM); inhibits the radial growth of M. gypsum, T. vercossum, and C....
Reference: SI-1000
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Harnessing the same gentle reliability as our market-leading DNA Transfection Reagents, we are proud to introduce to you FuGENE® SI, an innovative RNA Transfection reagent engineered for the delivery of siRNA. FuGENE®...
Reference: 22184-5
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A monoterpene with diverse biological activities; reduces compound action potential (CAP) peak amplitude in isolated frog sciatic nerves (IC50 = 0.51 mM); inhibits the radial growth of M. gypsum, T. vercossum, and C....
Reference: SI-5000
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Harnessing the same gentle reliability as our market-leading DNA Transfection Reagents, we are proud to introduce to you FuGENE® SI, an innovative RNA Transfection reagent engineered for the delivery of siRNA. FuGENE®...
Reference: 23159-100
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A monoterpene with diverse biological activities; inhibits the growth of S. typhimurium, E. coli, L. monocytogenes, S. epidermidis, and S. aureus (MICs = 0.266-0.608% v/v); decreases the invasive activity of HT-1080...
Reference: LJU-CIN-5
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Actiflash is a photo-inducible tamoxifen analogue. Upon UV-light irradiation, the compound activates your chosen ERT2 protein fusion. It can be used to control transcription (using Gal4-UAS) or induce recombination...
Reference: 23161-100
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A monoterpene with diverse biological activities; antibacterial activity against S. aureus, E. faecium, E. coli, and M. smegmatis (MICs = 0.78, 12.5, 0.78, and 1.56 μl/ml, respectively, in an agar diffusion assay) and...
Reference: LJU-CIN-50
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Actiflash is a photo-inducible tamoxifen analogue. Upon UV-light irradiation, the compound activates your chosen ERT2 protein fusion. It can be used to control transcription (using Gal4-UAS) or induce recombination...
Reference: 23161-25
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A monoterpene with diverse biological activities; antibacterial activity against S. aureus, E. faecium, E. coli, and M. smegmatis (MICs = 0.78, 12.5, 0.78, and 1.56 μl/ml, respectively, in an agar diffusion assay) and...
Reference: EXP-711-11-1ml
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293 Expression MAX-1 is expressed from - -.
Reference: 23161-250
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A monoterpene with diverse biological activities; antibacterial activity against S. aureus, E. faecium, E. coli, and M. smegmatis (MICs = 0.78, 12.5, 0.78, and 1.56 μl/ml, respectively, in an agar diffusion assay) and...
Reference: 23161-50
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A monoterpene with diverse biological activities; antibacterial activity against S. aureus, E. faecium, E. coli, and M. smegmatis (MICs = 0.78, 12.5, 0.78, and 1.56 μl/ml, respectively, in an agar diffusion assay) and...
Reference: DIV000F1
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These fluorescent nanoparticles are designed for efficient cellular uptake, a key aspect in cellular biology and drug delivery research. Ideal for live cell imaging and therapeutic applications, this reagent ensures...
Reference: 23722-100
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A monoterpene with diverse biological activities; scavenges DPPH and ABTS+ free radicals (IC50s = 2.8 and 30 mM, respectively); reduces APPH-induced hemolysis in isolated human erythrocytes; reduces the growth of T....
Reference: DIV010
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Our Nanoparticle Reagent for Small Molecule Delivery revolutionizes drug delivery systems, increasing solubility of hydrophobic compounds and catering amphiphilic and hydrophilic drugs. This lipid nanoparticles...
Reference: 23722-250
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A monoterpene with diverse biological activities; scavenges DPPH and ABTS+ free radicals (IC50s = 2.8 and 30 mM, respectively); reduces APPH-induced hemolysis in isolated human erythrocytes; reduces the growth of T....
Reference: DIV010F1
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The Fluorescent Nanoparticle Reagent for Small Molecule Delivery is a groundbreaking tool in molecular biology and pharmacology. Its utilization of lipid nanoemulsions allows for high fluorescence and non-toxic...
Reference: 23722-500
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A monoterpene with diverse biological activities; scavenges DPPH and ABTS+ free radicals (IC50s = 2.8 and 30 mM, respectively); reduces APPH-induced hemolysis in isolated human erythrocytes; reduces the growth of T....
Reference: DIV042
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Our Nanoparticle Reagent for Peptide Delivery, based on biocompatible lipids that ensure an efficient interaction with anionic peptides, is essential for advanced peptide therapeutics and for the development of...
Reference: AG-CN2-0001-M001
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Non-peptidic anti-diabetic agent. Receptor-selective glucagon antagonist. Free radical species (·OH, R·) and singlet oxygen (1O2) scavenger. Mycotoxin. Cytotoxic. Antioxidant. Inhibitor of botulinum neurotoxin...
Reference: DIV042F1
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The Fluorescent Nanoparticle Reagent for Peptide Delivery (anionic and negatively charged) utilizing lipid nanoemulsions, emerges as a key asset in biomolecular engineering and peptide therapeutics. With its high...
Reference: AG-CN2-0011-M001
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Prenylated 4-hydroxycoumarin. Anti-tumor compound. Cytotoxic. Stimulator of tubulin polymerization in vitro. Inhibitor of colchicine binding to tubulin. Antitubercular antibiotic with potent antibacterial activity....
Reference: DIV031
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Our Nanoparticle Reagent for Protein Targeted Delivery, leveraging lipid nanoemulsions, is a cornerstone in protein cell internalization. Designed for precision biomedicine and therapeutic evaluation, it facilitates...
Reference: AG-CN2-0011-M005
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Prenylated 4-hydroxycoumarin. Anti-tumor compound. Cytotoxic. Stimulator of tubulin polymerization in vitro. Inhibitor of colchicine binding to tubulin. Antitubercular antibiotic with potent antibacterial activity....
Reference: DIV031F1
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The Fluorescent Nanoparticle Reagent for Protein Delivery is a breakthrough in protein therapeutics and fluorescence imaging. It ensures effective delivery of protein-loaded nanoemulsions, pivotal for research in...
Reference: AG-CN2-0011-M010
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Prenylated 4-hydroxycoumarin. Anti-tumor compound. Cytotoxic. Stimulator of tubulin polymerization in vitro. Inhibitor of colchicine binding to tubulin. Antitubercular antibiotic with potent antibacterial activity....
Reference: DIV053
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Our Nanoparticle Reagent for Precision RNA Therapy Delivery is a cornerstone in gene therapy and molecular biology. It enables efficient mRNA transfection in cells, including primary cultures and organoids....
Reference: AG-CN2-0018-M005
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Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
Reference: DIV053F1
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The Fluorescent Nanoparticle Reagent for RNA Therapy Delivery is a key tool in RNA-based therapeutics and cellular imaging. With a high transfection efficiency, it allows for the tracking of mRNA delivery in live and...
Reference: AG-CN2-0018-M010
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Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
Reference: AG-CN2-0018-M025
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Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
Reference: AG-CN2-0019-C100
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Antibiotic. PKC, PKA and PKG inhibitor. Shows neurotropic activity by inducing neurite outgrowth. Highly potent cell permeable CaM kinase and phosphorylase inhibitor. Tyrosine protein kinase inhibitor of the TRK...
Reference: AG-CN2-0019-M001
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Antibiotic. PKC, PKA and PKG inhibitor. Shows neurotropic activity by inducing neurite outgrowth. Highly potent cell permeable CaM kinase and phosphorylase inhibitor. Tyrosine protein kinase inhibitor of the TRK...
Reference: AG-CN2-0020-M005
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Antibiotic. High affinity ionophore for monovalent cations such as H+, K+, Na+, Pb2+. Shows antibacterial (Gram-positive), antifungal, antitumor and antiviral activity. Disrupts membrane potential of mitochondria....
Reference: AG-CN2-0020-M025
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Antibiotic. High affinity ionophore for monovalent cations such as H+, K+, Na+, Pb2+. Shows antibacterial (Gram-positive), antifungal, antitumor and antiviral activity. Disrupts membrane potential of mitochondria....
Reference: AG-CN2-0021-M001
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Antibiotic. Protein tyrosine kinase inhibitor. Has antifungal, antimalarial, antiangiogenic (in vivo), anti-inflammatory and antiviral activity. Cyclooxygenase-2 (COX-2) expression inhibitor without affecting COX-1...
Reference: AG-CN2-0021-M005
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Antibiotic. Protein tyrosine kinase inhibitor. Has antifungal, antimalarial, antiangiogenic (in vivo), anti-inflammatory and antiviral activity. Cyclooxygenase-2 (COX-2) expression inhibitor without affecting COX-1...
Reference: AG-CN2-0022-C100
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Antibiotic. Antifungal and anti-yeast activity. Inhibits platelet aggregation induced by collagen or ADP. Has no effect on thrombin-induced platelet aggregation. Potent, cell permeable, reversible, ATP-competitive and...
Reference: AG-CN2-0022-C500
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Antibiotic. Antifungal and anti-yeast activity. Inhibits platelet aggregation induced by collagen or ADP. Has no effect on thrombin-induced platelet aggregation. Potent, cell permeable, reversible, ATP-competitive and...
Reference: AG-CN2-0022-M001
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Antibiotic. Antifungal and anti-yeast activity. Inhibits platelet aggregation induced by collagen or ADP. Has no effect on thrombin-induced platelet aggregation. Potent, cell permeable, reversible, ATP-competitive and...
Reference: AG-CN2-0022-M005
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Antibiotic. Antifungal and anti-yeast activity. Inhibits platelet aggregation induced by collagen or ADP. Has no effect on thrombin-induced platelet aggregation. Potent, cell permeable, reversible, ATP-competitive and...
Reference: AG-CN2-0023-M001
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Antibiotic. Potent anti-neutrophil agent with cardioprotective effects. mTOR, DNA-PK, phosphatidylinositol 4-kinases, myosin light chain kinase (MLCK) and mitogen-activated protein kinase (MAPK) inhibitor at high...
Reference: AG-CN2-0023-M005
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Antibiotic. Potent anti-neutrophil agent with cardioprotective effects. mTOR, DNA-PK, phosphatidylinositol 4-kinases, myosin light chain kinase (MLCK) and mitogen-activated protein kinase (MAPK) inhibitor at high...
Reference: AG-CN2-0023-M025
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Antibiotic. Potent anti-neutrophil agent with cardioprotective effects. mTOR, DNA-PK, phosphatidylinositol 4-kinases, myosin light chain kinase (MLCK) and mitogen-activated protein kinase (MAPK) inhibitor at high...
Reference: AG-CN2-0025-C100
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Antibiotic. Antibacterial and antifungal properties. Forms a complex with FKBP12 and inhibits the mammalian target of rapamycin (mTOR). Inhibits the response to interleukin-2 (IL-2), and thereby blocks activation of T...
Reference: AG-CN2-0025-M001
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Antibiotic. Antibacterial and antifungal properties. Forms a complex with FKBP12 and inhibits the mammalian target of rapamycin (mTOR). Inhibits the response to interleukin-2 (IL-2), and thereby blocks activation of T...
Reference: AG-CN2-0025-M005
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Antibiotic. Antibacterial and antifungal properties. Forms a complex with FKBP12 and inhibits the mammalian target of rapamycin (mTOR). Inhibits the response to interleukin-2 (IL-2), and thereby blocks activation of T...
Reference: AG-CN2-0025-M025
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Antibiotic. Antibacterial and antifungal properties. Forms a complex with FKBP12 and inhibits the mammalian target of rapamycin (mTOR). Inhibits the response to interleukin-2 (IL-2), and thereby blocks activation of T...
Reference: AG-CN2-0030-M250
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Antibiotic. Cytotoxic to prokaryotic and eukaryotic cells by inhibiting the protein synthesis. Apoptosis inducer. Widely employed in the selection of eukaryotic expression vectors, in combination with either...
Reference: AG-CN2-0030-M500
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Antibiotic. Cytotoxic to prokaryotic and eukaryotic cells by inhibiting the protein synthesis. Apoptosis inducer. Widely employed in the selection of eukaryotic expression vectors, in combination with either...
Reference: AG-CN2-0030-G001
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Antibiotic. Cytotoxic to prokaryotic and eukaryotic cells by inhibiting the protein synthesis. Apoptosis inducer. Widely employed in the selection of eukaryotic expression vectors, in combination with either...
Reference: AG-CN2-0030-G005
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Antibiotic. Cytotoxic to prokaryotic and eukaryotic cells by inhibiting the protein synthesis. Apoptosis inducer. Widely employed in the selection of eukaryotic expression vectors, in combination with either...
Reference: AG-CN2-0040-M001
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Antibiotic. Antibacterial (weak). Anticancer compound (weak).
Reference: AG-CN2-0043-M001
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Antibiotic. Apoptosis inducer. Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. Anticancer compound. Antihaptotactic and antimetastatic. Antiangiogenic compound. Antibacterial, antiprotozal, antiviral and...
Reference: AG-CN2-0043-M005
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Antibiotic. Apoptosis inducer. Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. Anticancer compound. Antihaptotactic and antimetastatic. Antiangiogenic compound. Antibacterial, antiprotozal, antiviral and...
Reference: AG-CN2-0046-M050
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Antibiotic. Diabetogenic. Diabetes inducer. Induces diabetes mellitus in animal models through its toxic effects on pancreatic beta-cells. Mutagenic. Potent alkylating agent. Potent DNA methylating agent. Nitric oxide...
Reference: AG-CN2-0046-M250
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Antibiotic. Diabetogenic. Diabetes inducer. Induces diabetes mellitus in animal models through its toxic effects on pancreatic beta-cells. Mutagenic. Potent alkylating agent. Potent DNA methylating agent. Nitric oxide...
Reference: AG-CN2-0046-G001
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Antibiotic. Diabetogenic. Diabetes inducer. Induces diabetes mellitus in animal models through its toxic effects on pancreatic beta-cells. Mutagenic. Potent alkylating agent. Potent DNA methylating agent. Nitric oxide...
Reference: AG-CN2-0054-MC05
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Antibiotic. Antibacterial. Weak antagonist of human endothelin receptor A (ETA) and B (ETB). Cholesteryl ester transfer protein (CETP) activity inhibitor. Grb2-Shc binding inhibitor. Potent aldose reductase inhibitor....
Reference: AG-CN2-0054-M001
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Antibiotic. Antibacterial. Weak antagonist of human endothelin receptor A (ETA) and B (ETB). Cholesteryl ester transfer protein (CETP) activity inhibitor. Grb2-Shc binding inhibitor. Potent aldose reductase inhibitor....
Reference: AG-CN2-0054-M005
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Antibiotic. Antibacterial. Weak antagonist of human endothelin receptor A (ETA) and B (ETB). Cholesteryl ester transfer protein (CETP) activity inhibitor. Grb2-Shc binding inhibitor. Potent aldose reductase inhibitor....
Reference: AG-CN2-0057-C010
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Antibiotic. Anticancer compound. Antifungal. Catalytic inhibitor of topoisomerase II (IC50 = 40 µM). Potent protein phosphatase 2A (PP2A) (IC50 = 1.5 nM) and 4 (PP4) (IC50 = 3 nM) inhibitor. Weak protein phosphatase...
Reference: AG-CN2-0065-M100
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Very potent polymyxin antibiotic. Has only one amino acid difference compared to polymyxin B. Antimicrobial. Targets the lipopolysaccharide (LPS) of the outer membrane of Gram-negative bacteria. Competitively...
Reference: AG-CN2-0065-G001
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Very potent polymyxin antibiotic. Has only one amino acid difference compared to polymyxin B. Antimicrobial. Targets the lipopolysaccharide (LPS) of the outer membrane of Gram-negative bacteria. Competitively...
Reference: AG-CN2-0065-G005
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Very potent polymyxin antibiotic. Has only one amino acid difference compared to polymyxin B. Antimicrobial. Targets the lipopolysaccharide (LPS) of the outer membrane of Gram-negative bacteria. Competitively...
Reference: AG-CN2-0066-G001
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Aminoglycoside antibiotic. Protein synthesis inhibitor. Causes codon misreading by binding to the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from the acceptor site to the donor site....
Reference: AG-CN2-0066-G005
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Aminoglycoside antibiotic. Protein synthesis inhibitor. Causes codon misreading by binding to the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from the acceptor site to the donor site....
Reference: AG-CN2-0066-G025
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Aminoglycoside antibiotic. Protein synthesis inhibitor. Causes codon misreading by binding to the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from the acceptor site to the donor site....
Reference: AG-CN2-0078-M025
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Aminonucleoside antibiotic. Protein synthesis inhibitor. Disrupts peptide transfer on ribosomes (acting as an acyl-tRNA analog) causing premature chain termination during translation. Translational inhibitor in...
Reference: AG-CN2-0078-M100
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Aminonucleoside antibiotic. Protein synthesis inhibitor. Disrupts peptide transfer on ribosomes (acting as an acyl-tRNA analog) causing premature chain termination during translation. Translational inhibitor in...
Reference: AG-CN2-0078-M250
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(tax incl.)
Aminonucleoside antibiotic. Protein synthesis inhibitor. Disrupts peptide transfer on ribosomes (acting as an acyl-tRNA analog) causing premature chain termination during translation. Translational inhibitor in...
Reference: AG-CN2-0078-M500
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(tax incl.)
Aminonucleoside antibiotic. Protein synthesis inhibitor. Disrupts peptide transfer on ribosomes (acting as an acyl-tRNA analog) causing premature chain termination during translation. Translational inhibitor in...