Lipid Controls
Avanti Polar Lipids 16:0 PC (DPPC), 63-89-8, 11g
Molecular Formula C40H80NO8P, Purity >99%, Formula Weight 734.039, 1,2-dipalmitoyl-sn-glycero-3-phosphocholine
Echelon Biosciences Research Labs CKK-E12 50MG
cKK-E12, 95% 50mg CAS#1432494-65-9 C60H120N4O6 MW:993.64
Avanti Polar Lipids 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-(6-azidohexanoyl) (ammonium salt), 2252461-34-8, 25 mg
Formula Weight: 848.145, Purity >99%, Storage Temperature: -20°C. This reagent is a modified lipid containing an omega-terminal azide. The terminal azide group can be used in a highly specific linking reaction with alkyne-containing reagents, known as ‘click chemistry’, in the presence of a copper (Cu)-containing catalyst.
Fujifilm Healthcare Americas Corp Hdl-Cholesterol E
The HDL-Cholesterol E kit is an in vitro assay utilizing a precipitation method for the quantitative determination of HDL cholesterol in serum. Package size: Kit includes: Precipitating Reagent - 1x 20 mL, Buffer Solution - 2 x 150 mL, Color Reagent- 2 x for 150 mL, Standard Solution - 1 x 10 mL bottles. This product is for Research Use Only, not for use in diagnostic procedures. Contact supplier for additional information at www.ivd.fujimed.com.
TARGETMOL CHEMICALS INC D-Lin-MC3-DMA 10MG
Also available in 1 mL, 1 mg, 5 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. D-Lin-MC3-DMA, an ionizable cationic lipid, serves as a potent siRNA delivery vehicle. Purity 97.18%
Cayman Chemical DLIn-MC3-DMA 100mg
An oxindole alkaloid with diverse biological activities inhibits decreases in cell viability and increases in intracellular levels of ROS and MDA induced by AB (25-35) in PC12 cells attenuates decreases in population spike amplitudes in the CA1 region of a rat hippocampal slice model of ischemia induced by oxygen and D-glucose deprivation at 30 and 100 M decreases the viability of HepG2 A549 BxPC-3 Caki-1 RPMI-8226 and 786-O cells (IC50s 130-292 M) induces apoptosis inhibits cell migration in a wound healing assay and decreases invasion in a Matrigel assay in HepG2 cells decreases right ventricular end systolic pressure hypertrophy and fibrosis in a rat model of monocrotaline-induced pulmonary arterial hypertension at 0.1 in the diet
Cayman Chemical 1 2-DIoleoyl-sn-glycerol 10mg
A cell-based luciferase reporter assay for estrogen receptor
Cayman Chemical 1 3DIoloyl2Stearoyl Glyce 10mg
An NMDA modulator with antagonist or agonist effects depending on brain region receptor composition and other factors an acetylated derivative of homotaurine decreases paired-pulse inhibition of GABAA IPSCs indicating that it may inhibit GABAB autoreceptor-mediated inhibition of GABA release (300 UM) reduces voluntary intake of ethanol in rats (0.26 and 0.52 mmol/kg per day i.p.)
Cayman Chemical 1 3DIstearoyl2oloyl Glyce 50mg
An alkaloid that has diverse biological activities reduces infarct size and collagen deposition and inhibits apoptosis of cardiomyocytes in a coronary artery ligation-induced rat model of myocardial infarction at 15 mg/kg per day increases hepatic levels of SOD and GSH reduces serum ALT and AST levels and inhibits hepatic fibrosis in a diet-induced mouse model of NASH at 200 mg/kg per day inhibits LPS-induced increases in TNF-a IL-1B and IL-6 levels in the serum of broiler chicks at 120 mg/kg
Cayman Chemical 1 3DIoleoyl2Decnoyl Glyce 5mg
A potent K-opioid receptor agonist (IC50s 5 6 and 1 2 nM for guinea pig and human receptors respectively) is 501- and 498-fold selective for K-opioid over - and -opioid receptors respectively is spasmolytic in isolated rat duodenum (IC50 4 2 M) and inhibits spontaneous contractions of isolated rat uterus (IC50 12 7 M) reduces joint damage in a rat model of CFA-induced arthritis reduces the abdominal withdrawal reflex in a model of visceral pain induced by colonic distension in wild-type mice at 25 mg/kg
Cayman Chemical 1 3DIstearoyl2oloyl Glyce 25mg
An alkaloid that has diverse biological activities reduces infarct size and collagen deposition and inhibits apoptosis of cardiomyocytes in a coronary artery ligation-induced rat model of myocardial infarction at 15 mg/kg per day increases hepatic levels of SOD and GSH reduces serum ALT and AST levels and inhibits hepatic fibrosis in a diet-induced mouse model of NASH at 200 mg/kg per day inhibits LPS-induced increases in TNF-a IL-1B and IL-6 levels in the serum of broiler chicks at 120 mg/kg
Cayman Chemical 1 3DIoctnoyl2Oleoyl Glyce 1mg
An inhibitor of VEGFRs (IC50s 0.38 0.02 0.18 and 0.23 M for human VEGFR1 2 3 and mouse Vegfr2 respectively) selective for VEGFRs over FGFRs and PDGFRa (IC50s 10 M) but has activity at PDGFRB (IC50 1.4 M) in an enzyme assay inhibits VEGF-induced VEGFR2 autophosphorylation (IC50 11.5 nM in CHO cells transfected with the human receptor) blocks bFGF- and VEGF-induced angiogenesis (ED50s 9 and 26 mg/kg respectively) in a mouse model of growth factor-induced angiogenesis
Cayman Chemical 1 3DIoctnoyl2Oleoyl Glyce 10mg
An antiprotozoal agent inhibits complex III activity on dihydroorotate in isolated P. falciparum and P. yoelii mitochondria more potently than in rat liver mitochondria (EC50s 0.95 0.94 and 510 nM respectively) depolarizes the mitochondrial membrane in P. yoelii-infected mouse erythrocytes (EC50 260 nM) inhibits human BCRP- and P-glycoprotein-mediated transport in membrane vesicles (IC50s 0.23 and 6.8 M respectively) inhibits the growth of T. gondii in MRC-5 human lung fibroblasts in vitro (IC50 ~64 nM) increases mean survival of T. gondii-infected mice from 5.5 to 21.2 days (100 mg/kg per day)
Cayman Chemical 1 3-DIoleoyl Glycerol 10mg
An antiviral guanosine analog has activity against multiple laboratory and clinical isolate strains of HSV-1 HSV-2 and VZV in a plaque reduction assay (IC50s 0.4-3.1 g/ml) inhibits HSV-1 and HSV-2 replication (IC99s 0.4 and 0.7 g/ml respectively) and DNA synthesis (IC50 0.04 g/ml) in MRC-5 cells reduces the severity of skin lesions caused by HSV-1 in guinea pigs and mice prevents development of HSV-2-induced genital lesions in guinea pigs infected intravaginally