Category: Reagents

Reference: BVT-0065-M001
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Antibiotic. Antibacterial and antifungal. Antitumor compound. Germination inhibitor.
Reference: CDX-C0310-M100
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Biologically incactive urinary metabolite of Clarithromycin (oxidized by ozone), a macrolide antibiotic. Compound can be used as analytical reference material.
Reference: CDX-C0310-M025
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Biologically incactive urinary metabolite of Clarithromycin (oxidized by ozone), a macrolide antibiotic. Compound can be used as analytical reference material.
Reference: CDX-C0310-M010
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Biologically incactive urinary metabolite of Clarithromycin (oxidized by ozone), a macrolide antibiotic. Compound can be used as analytical reference material.
Reference: BVT-0458-M001
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Dimeric spiro-azaphilone. Mycotoxin.
Reference: AG-CN2-0512-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-CN2-0512-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-CN2-0512-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-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-CN2-0065-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-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: BVT-0237-M005
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Antibiotic. More potent and specific H+-ATPase inhibitor than bafilomycin A1 (Prod. No. BVT-0252). Inhibits acidification of organelles such as lysosomes and the Golgi apparatus. Inhibitor of autophagic degradation by...
Reference: BVT-0237-M001
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Antibiotic. More potent and specific H+-ATPase inhibitor than bafilomycin A1 (Prod. No. BVT-0252). Inhibits acidification of organelles such as lysosomes and the Golgi apparatus. Inhibitor of autophagic degradation by...
Reference: BVT-0237-C100
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Antibiotic. More potent and specific H+-ATPase inhibitor than bafilomycin A1 (Prod. No. BVT-0252). Inhibits acidification of organelles such as lysosomes and the Golgi apparatus. Inhibitor of autophagic degradation by...
Reference: BVT-0237-C025
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Antibiotic. More potent and specific H+-ATPase inhibitor than bafilomycin A1 (Prod. No. BVT-0252). Inhibits acidification of organelles such as lysosomes and the Golgi apparatus. Inhibitor of autophagic degradation by...
Reference: BVT-0253-M001
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Antibiotic. Exhibits similar activity as concanamycin A (Prod. No. BVT-0237) and concanamycin C (Prod. No. BVT-0254). Specific vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal...
Reference: BVT-0253-C500
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Antibiotic. Exhibits similar activity as concanamycin A (Prod. No. BVT-0237) and concanamycin C (Prod. No. BVT-0254). Specific vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal...
Reference: BVT-0253-C100
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Antibiotic. Exhibits similar activity as concanamycin A (Prod. No. BVT-0237) and concanamycin C (Prod. No. BVT-0254). Specific vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal...
Reference: BVT-0253-C025
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Antibiotic. Exhibits similar activity as concanamycin A (Prod. No. BVT-0237) and concanamycin C (Prod. No. BVT-0254). Specific vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal...
Reference: BVT-0254-M001
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Antibiotic. Vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal pH and thus inactivating the lysosomal acid hydrolases. Anti-osteoporotic. Antiviral. Immunosuppressive....
Reference: BVT-0254-C500
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Antibiotic. Vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal pH and thus inactivating the lysosomal acid hydrolases. Anti-osteoporotic. Antiviral. Immunosuppressive....
Reference: BVT-0254-C100
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Antibiotic. Vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal pH and thus inactivating the lysosomal acid hydrolases. Anti-osteoporotic. Antiviral. Immunosuppressive....
Reference: BVT-0254-C025
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Antibiotic. Vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal pH and thus inactivating the lysosomal acid hydrolases. Anti-osteoporotic. Antiviral. Immunosuppressive....
Reference: CDX-C0339-M100
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Cordycepin is a nucleoside (adenosine analog) antibiotic that acts as a polyadenylation inhibitor when converted to 3’-deoxyadenosine triphosphate (3'-dATP), which inhibits ATP-dependent DNA and RNA synthesis....
Reference: CDX-C0339-M025
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Cordycepin is a nucleoside (adenosine analog) antibiotic that acts as a polyadenylation inhibitor when converted to 3’-deoxyadenosine triphosphate (3'-dATP), which inhibits ATP-dependent DNA and RNA synthesis....
Reference: CDX-C0339-M010
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Cordycepin is a nucleoside (adenosine analog) antibiotic that acts as a polyadenylation inhibitor when converted to 3’-deoxyadenosine triphosphate (3'-dATP), which inhibits ATP-dependent DNA and RNA synthesis....
Reference: BVT-0462-M010
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Hydroquinone antibiotic. Antibacterial and antifungal activity.
Reference: BVT-0462-M005
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Hydroquinone antibiotic. Antibacterial and antifungal activity.
Reference: BVT-0462-M001
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Hydroquinone antibiotic. Antibacterial and antifungal activity.
Reference: AG-CN2-0147-M005
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Antibiotic. Antiprotozoal. Antifungal and phytotoxic compound. Anti-inflammatory. TGF-beta signaling inhibitor Anticancer compound. Inhibits expression of inducible nitric oxide synthase (iNOS; NOSII). Cell division...
Reference: AG-CN2-0147-M001
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Antibiotic. Antiprotozoal. Antifungal and phytotoxic compound. Anti-inflammatory. TGF-beta signaling inhibitor Anticancer compound. Inhibits expression of inducible nitric oxide synthase (iNOS; NOSII). Cell division...
Reference: BVT-0097-M001
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Phytotoxin. Microtubule assembly inhibitor. Similar to curvularin.
Reference: AG-CN2-0148-M005
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Antibiotic. Antimalaria agent.
Reference: AG-CN2-0148-M001
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Antibiotic. Antimalaria agent.
Reference: BVT-0447-M001
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Potent mycotoxin. Phytotoxin. Actin polymerization inhibitor. Used in actin polymerization and cytoskeletal reorganization studies. Antibacterial, antifungal, nematocidal and antitumor compound. Apoptosis inducer....
Reference: BVT-0450-M001
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Mycotoxin. Phytotoxic and cytotoxic agent. Immunosuppressive activity. Affects chromosome congression and spindle microtubule organization in PtK1 cells. Actin and myosin inhibitor.
Reference: CDX-D0356-G005
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D-cycloserine (DCS) is an antibiotic, inhibiting cell-wall biosynthesis in bacteria. It is a tuberculostatic agent, that inhibits L-alanine racemase and D-alanine:D-alanine ligase, enzymes essential to peptidoglycan...
Reference: CDX-D0356-G001
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D-cycloserine (DCS) is an antibiotic, inhibiting cell-wall biosynthesis in bacteria. It is a tuberculostatic agent, that inhibits L-alanine racemase and D-alanine:D-alanine ligase, enzymes essential to peptidoglycan...
Reference: BVT-0283-M001
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Hypolipidemic. Cholesterol biosynthesis inhibitor.
Reference: BVT-0030-M005
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Nucleoside antibiotic. Antitumor compound. Xanthosine monophosphate (XMP) aminase inhibitor. RNA synthesis inhibitor. Specific GMP synthase inhibitor. Reduces intracellular GTP levels.
Reference: BVT-0030-M001
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Nucleoside antibiotic. Antitumor compound. Xanthosine monophosphate (XMP) aminase inhibitor. RNA synthesis inhibitor. Specific GMP synthase inhibitor. Reduces intracellular GTP levels.
Reference: BVT-0158-M001
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Derivative of the farnesyltransferase inhibitor Manumycin A (Prod. No. BVT-0091 http://www.adipogen.com/bvt-0091/manumycin-a.html ). This compound has not yet been thoroughly tested for its biological activity.
Reference: BVT-0112-M005
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Polyhydroxylated piperidine alkaloid. alpha-Glucosidase I and II inhibitor. Antidiabetic. Antihyperglycaemic activity. Animal feedstuff additive. Antiviral. Shows anti-HIV activity.
Reference: BVT-0112-M001
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Polyhydroxylated piperidine alkaloid. alpha-Glucosidase I and II inhibitor. Antidiabetic. Antihyperglycaemic activity. Animal feedstuff additive. Antiviral. Shows anti-HIV activity.
Reference: BVT-0381-M001
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Antibiotic. Antibacterial. Inducer of Friend mouse erythroleukemia cells. Antitumor compound.
Reference: BVT-0381-C500
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Antibiotic. Antibacterial. Inducer of Friend mouse erythroleukemia cells. Antitumor compound.
Reference: BVT-0401-M001
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Signal substance. Microbial bioregulator.
Reference: BVT-0401-C500
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Signal substance. Microbial bioregulator.
Reference: BVT-0228-M001
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Isochromane quinone antibiotic. Antibacterial. Inhibits Trichomonas vaginalis (in vitro and in vivo). Inhibitor of the RNA synthesis.
Reference: BVT-0414-M001
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Derivative of the farnesyltransferase inhibitor Manumycin A (Prod. No. BVT-0091 http://www.adipogen.com/bvt-0091/manumycin-a.html ). This compound has not yet been thoroughly tested for its biological activity.
Reference: BVT-0468-M100
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Naturally occurring organosulfur compound. Osmolyte, osmoprotectant. Antioxidant. Cryoprotectant. Neuroprotective agent. Neuritogenic. Acts against immune-deficient diseases (e.g. cancer). Important in geochemistry,...
Reference: BVT-0267-M005
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Antibiotic. Antitumor compound. Powerful, selective inhibitor of nucleic acid synthesis in vitro. Potent hypoxia-inducible factor 1 (HIF-1) DNA binding activity inhibitor. Apoptosis inducer. Antibacterial, antifungal...
Reference: BVT-0267-M001
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Antibiotic. Antitumor compound. Powerful, selective inhibitor of nucleic acid synthesis in vitro. Potent hypoxia-inducible factor 1 (HIF-1) DNA binding activity inhibitor. Apoptosis inducer. Antibacterial, antifungal...
Reference: BVT-0006-M005
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Antibiotic. Cell cycle inhibitor at the G(2)/M phase. Antitumor compound. Apoptosis inducer.
Reference: BVT-0006-M001
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Antibiotic. Cell cycle inhibitor at the G(2)/M phase. Antitumor compound. Apoptosis inducer.
Reference: BVT-0185-M001
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Antibiotic. Active against Gram-positive bacteria, protozoa and tumors. Testosterone 5alpha-reductase inhibitor. Nitric oxide synthase (NOS) inhibitor. Immunosuppressive. Enhances the antifungal activity of rapamycin.
Reference: BVT-0342-M005
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Inhibitor of human leukocyte elastase (IC50 = 1.3 µg/ml), different other elastases and chymotrypsin (IC50 = 82 µg/ml).
Reference: BVT-0342-M001
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Inhibitor of human leukocyte elastase (IC50 = 1.3 µg/ml), different other elastases and chymotrypsin (IC50 = 82 µg/ml).
Reference: BVT-0198-M005
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Antibiotic. Antibacterial. Moderate cytotoxic.
Reference: BVT-0198-M001
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Antibiotic. Antibacterial. Moderate cytotoxic.
Reference: AG-CN2-0477-MC05
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Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic. Incorporation into the cell membrane forms...
Reference: AG-CN2-0478-M001
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Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic. Incorporation into the cell membrane forms...
Reference: AG-CN2-0479-M001
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Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic (less ionophoric than Enniatin A). Incorporation...
Reference: AG-CN2-0480-M001
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Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic. Incorporation into the cell membrane forms...
Reference: AG-CN2-0116-M001
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Potent antibiotic. Bacteriocin. Antibacterial. Broad spectrum activity against Gram-positive and Gram-negative bacteria. Herbicidal. Enterocin is a small molecular weight secondary metabolite and should not be...
Reference: AG-CN2-0116-C250
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Potent antibiotic. Bacteriocin. Antibacterial. Broad spectrum activity against Gram-positive and Gram-negative bacteria. Herbicidal. Enterocin is a small molecular weight secondary metabolite and should not be...
Reference: AG-CN2-0422-C500
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Antibiotic. Potent anticancer compound. Cell permeable, potent, selective and irreversible 20S proteasome inhibitor. Predominantly inhibits the chymotrypsin-like (CTRL) activity of the proteasome. Exhibits lower level...
Reference: AG-CN2-0422-C250
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Antibiotic. Potent anticancer compound. Cell permeable, potent, selective and irreversible 20S proteasome inhibitor. Predominantly inhibits the chymotrypsin-like (CTRL) activity of the proteasome. Exhibits lower level...
Reference: AG-CN2-0422-C100
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Antibiotic. Potent anticancer compound. Cell permeable, potent, selective and irreversible 20S proteasome inhibitor. Predominantly inhibits the chymotrypsin-like (CTRL) activity of the proteasome. Exhibits lower level...
Reference: AG-CN2-0422-C050
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Antibiotic. Potent anticancer compound. Cell permeable, potent, selective and irreversible 20S proteasome inhibitor. Predominantly inhibits the chymotrypsin-like (CTRL) activity of the proteasome. Exhibits lower level...
Reference: BVT-0433-M001
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Eremophilane sesquiterpene. Nontoxic secondary metabolite from Penicillium roqueforti.
Reference: BVT-0436-M001
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Eremophilane sesquiterpene. Nontoxic secondary metabolite from Penicillium roqueforti.
Reference: CDX-E0237-G100
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Ethionamide is an antimycobacterial antibiotic that is active against M. tuberculosis (MICs = 0.3-1.25 µg/ml). Ethionamide is a prodrug activated via oxidation by ethA (a flavin monooxygenase) and leading to the...
Reference: CDX-E0237-G025
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Ethionamide is an antimycobacterial antibiotic that is active against M. tuberculosis (MICs = 0.3-1.25 µg/ml). Ethionamide is a prodrug activated via oxidation by ethA (a flavin monooxygenase) and leading to the...
Reference: CDX-E0237-G005
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Ethionamide is an antimycobacterial antibiotic that is active against M. tuberculosis (MICs = 0.3-1.25 µg/ml). Ethionamide is a prodrug activated via oxidation by ethA (a flavin monooxygenase) and leading to the...
Reference: CDX-E0074-M250
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Potent immunosuppressant. Binds with high affinity to the FK506 binding protein-12 (FKBP-12) to generate an immunosuppressive complex that inhibits the...
Reference: CDX-E0074-M100
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Potent immunosuppressant. Binds with high affinity to the FK506 binding protein-12 (FKBP-12) to generate an immunosuppressive complex that inhibits the...
Reference: AG-CN2-0520-M025
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Orally available Rapamycin derivative that shows improved pharmacokinetics and pharmacodynamics. Potent immunosuppressant. Binds with high affinity to the...
Reference: AG-CN2-0520-M005
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Orally available Rapamycin derivative that shows improved pharmacokinetics and pharmacodynamics. Potent immunosuppressant. Binds with high affinity to the...
Reference: AG-CN2-0520-M001
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Orally available Rapamycin derivative that shows improved pharmacokinetics and pharmacodynamics. Potent immunosuppressant. Binds with high affinity to the...
Reference: CDX-E0574-M001
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Potent immunosuppressant. Binds with high affinity to the FK506 binding protein-12 (FKBP-12) to generate an immunosuppressive complex that inhibits the...
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: 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: 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: CDX-F0079-G025
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Flumequine is a fluoroquinolone synthetic chemotherapeutic antibiotic used to treat bacterial infections. Targets primarily gram negative bacteria, especially those which cause enteric infections in animals. It is...
Reference: CDX-F0079-G005
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Flumequine is a fluoroquinolone synthetic chemotherapeutic antibiotic used to treat bacterial infections. Targets primarily gram negative bacteria, especially those which cause enteric infections in animals. It is...
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: BVT-0469-M001
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C-glycosidic angucyclinone derivative. Antibiotic. Antitumor agent. Antibacterial agent. Isomer of fridamycin B (Prod. No. BVT-0470).
Reference: BVT-0470-M001
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C-glycosidic angucyclinone derivative. Antibiotic. Antitumor agent. Antibacterial agent. Isomer of fridamycin A (Prod. No. BVT-0469).
Reference: BVT-0472-M001
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Anthraquinone derivative derived from an angucyclinone precursor. Antibiotic. Antibacterial agent.
Reference: AG-CN2-0529-M025
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Meroterpenoid antibiotic. Anticancer, antimicrobial, antimalarial and amoebicidal compound. Potent, selective and covalent inhibitor of methionine aminopeptidase-2 (MetAP2). Anti-angiogenic by impairing the growth of...
Reference: AG-CN2-0529-M005
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Meroterpenoid antibiotic. Anticancer, antimicrobial, antimalarial and amoebicidal compound. Potent, selective and covalent inhibitor of methionine aminopeptidase-2 (MetAP2). Anti-angiogenic by impairing the growth of...
Reference: AG-CN2-0529-M001
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Meroterpenoid antibiotic. Anticancer, antimicrobial, antimalarial and amoebicidal compound. Potent, selective and covalent inhibitor of methionine aminopeptidase-2 (MetAP2). Anti-angiogenic by impairing the growth of...
Reference: BVT-0090-M005
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Ergot alkaloid. Mycotoxin.
Reference: BVT-0090-M001
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Ergot alkaloid. Mycotoxin.
Reference: BVT-0189-M001
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Mycotoxin. Cytotoxic. Tremorgenic. Potent and specific inhibitor of the breast cancer resistance protein (BCRP; ABCG2). Reverses multidrug resistance mediated by BCRP and increases cytotoxicity of several anticancer...
Reference: BVT-0189-C250
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Mycotoxin. Cytotoxic. Tremorgenic. Potent and specific inhibitor of the breast cancer resistance protein (BCRP; ABCG2). Reverses multidrug resistance mediated by BCRP and increases cytotoxicity of several anticancer...
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-CN2-0030-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-M500
€0.00 (tax incl.)
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...

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