Category: Reagents

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: 10006197-100
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An internal standard for the quantification of LTA4 methyl ester by GC- or LC-MS
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: 10006197-25
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An internal standard for the quantification of LTA4 methyl ester by GC- or LC-MS
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: 10006197-50
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An internal standard for the quantification of LTA4 methyl ester by GC- or LC-MS
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: 10006198-100
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An internal standard for the quantification of LTC4 by GC- or LC-MS
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: 10006198-25
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An internal standard for the quantification of LTC4 by GC- or LC-MS
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: 10006198-50
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An internal standard for the quantification of LTC4 by GC- or LC-MS
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: 10006199-100
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An internal standard for the quantification of LTD4 by GC- or LC-MS.
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: 10006199-25
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An internal standard for the quantification of LTD4 by GC- or LC-MS.
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: 10006199-50
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An internal standard for the quantification of LTD4 by GC- or LC-MS.
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: 10006410-100
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An internal standard for the quantification of (±)14(15)-EET by GC- or LC-MS
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: 10006410-25
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An internal standard for the quantification of (±)14(15)-EET by GC- or LC-MS
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: 10006410-50
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An internal standard for the quantification of (±)14(15)-EET by GC- or LC-MS
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: 10006413-10
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An iternal standard for the quantification of ±11(12)-EET by GC- or LC-MS
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: 10006413-100
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An iternal standard for the quantification of ±11(12)-EET by GC- or LC-MS
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: 10006413-25
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An iternal standard for the quantification of ±11(12)-EET by GC- or LC-MS
Reference: AG-CN2-0078-M250
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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: 10006413-50
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An iternal standard for the quantification of ±11(12)-EET by GC- or LC-MS
Reference: AG-CN2-0078-M500
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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: 10006556-1
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An internal standard for the quantification of Latanoprost by GC- or LC-MS.
Reference: AG-CN2-0078-G001
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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: 10006556-100
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An internal standard for the quantification of Latanoprost by GC- or LC-MS.
Reference: AG-CN2-0088-C100
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Antibiotic. Caffeine-like Ca2+ releaser in heavy sarcoplasmic reticulum (HSR). Antifungal. Chitinase inhibitor. DNA methyltransferase inhibitor. Histone deacetylase (HDAC) inhibitor. Anticancer compound. Angiogenesis...
Reference: 10006556-50
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An internal standard for the quantification of Latanoprost by GC- or LC-MS.
Reference: AG-CN2-0091-C250
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Antibiotic. DNA helicase inhibitor. Inhibits the DNA helicase activity of the human minichromosome maintenance (MCM) 4/6/7 complex. Topoisomerase I and II inhibitor (weaker than DNA helicase). DNA and RNA synthesis...
Reference: 10006556-500
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An internal standard for the quantification of Latanoprost by GC- or LC-MS.
Reference: AG-CN2-0091-C500
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Antibiotic. DNA helicase inhibitor. Inhibits the DNA helicase activity of the human minichromosome maintenance (MCM) 4/6/7 complex. Topoisomerase I and II inhibitor (weaker than DNA helicase). DNA and RNA synthesis...
Reference: 10006654-10
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An internal standard for the quantification of (±)5-iPF2α-VI by GC- or LC-MS.
Reference: AG-CN2-0097-M001
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Indolocarbazole alkaloid antibiotic.. Potent cell permeable reversible and ATP-competitive PKC (protein kinase C) inhibitor with 10-fold selectivity over PKA (protein kinase A). Anticancer compound. Cytotoxic againt...
Reference: 10006654-25
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An internal standard for the quantification of (±)5-iPF2α-VI by GC- or LC-MS.
Reference: AG-CN2-0097-M005
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Indolocarbazole alkaloid antibiotic.. Potent cell permeable reversible and ATP-competitive PKC (protein kinase C) inhibitor with 10-fold selectivity over PKA (protein kinase A). Anticancer compound. Cytotoxic againt...
Reference: 10006758-1
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An internal standard for the quantification of arachidonic acid by GC- or LC-MS
Reference: AG-CN2-0100-C250
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Antibiotic. Antifungal. Potent and specific mitochondrial complex II (succinate-ubiquinone oxidoreductase) inhibitor. Mitochondrial ATP-sensitive potassium (mK(ATP)) channel activator. Cardioprotective. Modulates...
Reference: 10006758-100
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An internal standard for the quantification of arachidonic acid by GC- or LC-MS
Reference: AG-CN2-0100-M001
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Antibiotic. Antifungal. Potent and specific mitochondrial complex II (succinate-ubiquinone oxidoreductase) inhibitor. Mitochondrial ATP-sensitive potassium (mK(ATP)) channel activator. Cardioprotective. Modulates...
Reference: 10006758-250
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An internal standard for the quantification of arachidonic acid by GC- or LC-MS
Reference: AG-CN2-0101-M001
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Antibiotic. Antiprotozoal. Antimicrobial. Cytotoxic and genotoxic in various mammalian cells. Mitochondrial permeability transition pore (MPTP) activator. Apoptosis inducer. ERK and JNK signaling pathways activator....
Reference: 10006758-500
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An internal standard for the quantification of arachidonic acid by GC- or LC-MS
Reference: AG-CN2-0101-M005
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Antibiotic. Antiprotozoal. Antimicrobial. Cytotoxic and genotoxic in various mammalian cells. Mitochondrial permeability transition pore (MPTP) activator. Apoptosis inducer. ERK and JNK signaling pathways activator....
Reference: 10006829-1
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The DHA Quant-PAK has been designed for the convenient, precise quantification of DHA by GC- or LC-MS. It includes a 50 µg vial of DHA-d5 and a precisely weighed vial of unlabeled DHA, with the precise weight (2-4 mg)...
Reference: AG-CN2-0101-M025
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Antibiotic. Antiprotozoal. Antimicrobial. Cytotoxic and genotoxic in various mammalian cells. Mitochondrial permeability transition pore (MPTP) activator. Apoptosis inducer. ERK and JNK signaling pathways activator....
Reference: 10006830-1
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The 6-keto PGF1α Quant-PAK has been designed for the convenient, precise quantification of 6-keto PGF1α by GC- or LC-MS. It includes a 50 µg vial of 6-keto PGF1α-d4 and a precisely weighed vial of unlabeled 6-keto...
Reference: AG-CN2-0103-MC05
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beta-Lactone antibiotic. Antibacterial and antifungal. Specific and irreversible inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase in vitro and in vivo by covalently modifying the active Cys129...
Reference: 10006831-1
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The 11-dehydro TXB2 Quant-PAK has been designed for the convenient, precise quantification of 11-dehydro TXB2 by GC- or LC-MS. It includes a 50 µg vial of 11-dehydro TXB2-d4 and a precisely weighed vial of unlabeled...
Reference: AG-CN2-0103-M001
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beta-Lactone antibiotic. Antibacterial and antifungal. Specific and irreversible inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase in vitro and in vivo by covalently modifying the active Cys129...
Reference: 10006832-1
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The TXB2 Quant-PAK has been designed for the convenient, precise quantification of TXB2 by GC- or LC-MS. It includes a 50 µg vial of TXB2-d4 and a precisely weighed vial of unlabeled TXB2, with the precise weight (2-4...
Reference: AG-CN2-0103-MM25
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beta-Lactone antibiotic. Antibacterial and antifungal. Specific and irreversible inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase in vitro and in vivo by covalently modifying the active Cys129...
Reference: 10006833-1
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The ω-3 arachidonic acid Quant-PAK has been designed for the convenient, precise quantification of ω-3 arachidonic acid by GC- or LC-MS. It includes a 50 µg vial of ω-3 arachidonic acid-d8 and a precisely weighed vial...
Reference: AG-CN2-0105-C250
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Red-pigmented antibiotic. Antimalarial. Immunosuppressive. Apoptosis inducer. Cytotoxic. Induces phosphorylation of p38-MAPK. Antimetastatic. Tumor invasion inhibitor. Induces p21WAF1/CIP1 expression. Anticancer...
Reference: 10006834-1
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The linoleic acid Quant-PAK has been designed for the convenient, precise quantification of linoleic acid by GC- or LC-MS. It includes a 50 µg vial of linoleic acid-d4 and a precisely weighed vial of unlabeled...
Reference: AG-CN2-0105-M001
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Red-pigmented antibiotic. Antimalarial. Immunosuppressive. Apoptosis inducer. Cytotoxic. Induces phosphorylation of p38-MAPK. Antimetastatic. Tumor invasion inhibitor. Induces p21WAF1/CIP1 expression. Anticancer...
Reference: 10006835-1
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The arachidonic acid Quant-PAK has been designed for the convenient, precise quantification of arachidonic acid by GC- or LC-MS. It includes a 50 µg vial of arachidonic acid-d8 and a precisely weighed vial of...
Reference: AG-CN2-0106-C250
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Antibiotic. Highly specific inhibitor of acyl-coenzyme A:cholesterol acetyltransferase 2 (ACAT2). Anti-angiogenic. Antiatherogenic and antiatherosclerotic agent. Shows cholesterol-lowering and atheroprotective...
Reference: 10006840-1
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The PGA2 Quant-PAK has been designed for the convenient, precise quantification of PGA2 by GC- or LC-MS. It includes a 50 µg vial of PGA2-d4 and a precisely weighed vial of unlabeled PGA2, with the precise weight...
Reference: AG-CN2-0106-M001
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Antibiotic. Highly specific inhibitor of acyl-coenzyme A:cholesterol acetyltransferase 2 (ACAT2). Anti-angiogenic. Antiatherogenic and antiatherosclerotic agent. Shows cholesterol-lowering and atheroprotective...
Reference: 10006841-1
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The PGB2 Quant-PAK has been designed for the convenient, precise quantification of PGB2 by GC- or LC-MS. It includes a 50 µg vial of PGB2-d4 and a precisely weighed vial of unlabeled PGB2, with the precise weight...
Reference: AG-CN2-0107-C250
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Peptide antibiotic. Induces root curvature and malformation in plants. Antibacterial, antimalarial and antitrypanosomal. Disrupts the cell cycle at the G2 checkpoint of cancer cells, leading to sensitization of the...
Reference: 10006842-1
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The PGD1 Quant-PAK has been designed for the convenient, precise quantification of PGD1 by GC- or LC-MS. It includes a 50 µg vial of PGD1-d4 and a precisely weighed vial of unlabeled PGD1, with the precise weight...
Reference: AG-CN2-0107-M001
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Peptide antibiotic. Induces root curvature and malformation in plants. Antibacterial, antimalarial and antitrypanosomal. Disrupts the cell cycle at the G2 checkpoint of cancer cells, leading to sensitization of the...
Reference: 10006843-1
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The PGD2 Quant-PAK has been designed for the convenient, precise quantification of PGD2 by GC- or LC-MS. It includes a 50 µg vial of PGD2-d4 and a precisely weighed vial of unlabeled PGD2, with the precise weight...
Reference: AG-CN2-0108-M001
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Antibiotic. Antifungal. Antiprotozoal. Potent and reversible, cell permeable inhibitor of histone deacetylase (HDAC). Immunosuppressive. Anticancer compound. Antifibrogenic. Apoptosis inducer. Induces cell growth...
Reference: 10006844-1
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The PGE1 Quant-PAK has been designed for the convenient, precise quantification of PGE1 by GC- or LC-MS. It includes a 50 µg vial of PGE1-d4 and a precisely weighed vial of unlabeled PGE1, with the precise weight (2-4...
Reference: AG-CN2-0108-M005
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Antibiotic. Antifungal. Antiprotozoal. Potent and reversible, cell permeable inhibitor of histone deacetylase (HDAC). Immunosuppressive. Anticancer compound. Antifibrogenic. Apoptosis inducer. Induces cell growth...
Reference: 10006845-1
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Contains a 50 µg vial of 13,14-dihydro PGE1-d4 and a precisely weighed vial of unlabeled 13,14-dihydro PGE1 (precise weight indicated on the vial) for the convenient, precise quantification of 13,14-dihydro PGE1 by...
Reference: AG-CN2-0112-C250
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Hydroxy-acid of antibiotic 1233A. Antibiotic. Antibacterial.
Reference: 10006846-1
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The PGE2 Quant-PAK has been designed for the convenient, precise quantification of PGE2 by GC- or LC-MS. It includes a 50 µg vial of PGE2-d4 and a precisely weighed vial of unlabeled PGE2, with the precise weight (2-4...
Reference: AG-CN2-0112-M001
€0.00 (tax incl.)
Hydroxy-acid of antibiotic 1233A. Antibiotic. Antibacterial.
Reference: 10006848-1
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The PGF2α Quant-PAK has been designed for the convenient, precise quantification of PGF2α by GC- or LC-MS. It includes a 50 µg vial of PGF2α-d4 and a precisely weighed vial of unlabeled PGF2α, with the precise weight...
Reference: AG-CN2-0113-C250
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Antibiotic. Hypotensive vasodilator. Calcium channel antagonist. Potent and selective CB1 receptor antagonist.
Reference: 10006850-1
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The 15-deoxy-.DELTA.12,14-PGJ2 Quant-PAK has been designed for the convenient, precise quantification of 15-deoxy-.DELTA.12,14-PGJ2 by GC- or LC-MS. It includes a 50 µg vial of 15-deoxy-.DELTA.12,14-PGJ2-d4 and a...
Reference: AG-CN2-0113-M001
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Antibiotic. Hypotensive vasodilator. Calcium channel antagonist. Potent and selective CB1 receptor antagonist.
Reference: 10006878-10
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An internal standard for the quantification of 8,12-iso-iPF2α-VI by GC- or LC-MS.
Reference: AG-CN2-0114-C250
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Antibiotic. Antibacterial. Antifungal. Anticancer compound. Inhibits anti-apoptotic functions regulated by Bcl-2. Circumvents arbekacin (ABK)-resistance in MRSA by inhibiting the bifunctional enzyme AAC(6')/APH(2'').
Reference: 10006878-25
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An internal standard for the quantification of 8,12-iso-iPF2α-VI by GC- or LC-MS.
Reference: AG-CN2-0114-M001
€0.00 (tax incl.)
Antibiotic. Antibacterial. Antifungal. Anticancer compound. Inhibits anti-apoptotic functions regulated by Bcl-2. Circumvents arbekacin (ABK)-resistance in MRSA by inhibiting the bifunctional enzyme AAC(6')/APH(2'').
Reference: 10006878-50
€0.00 (tax incl.)
An internal standard for the quantification of 8,12-iso-iPF2α-VI by GC- or LC-MS.
Reference: AG-CN2-0116-C250
€0.00 (tax incl.)
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: 10006974-10
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An inverse agonist at CB2 and partial agonist at CB1 receptors; binds selectively to CB2 over CB1 receptors (Kis = 31.2 and 5,152 nM, respectively); blocks the antinociceptive effects of cannabinoids; decreases...

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