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Human sera and related serum-derived preparations are used in cell culture, immunoassays, and other laboratory research. Depending on the preparation, they may supplement culture media or serve as blocking reagents and assay controls.
A sesquiterpene lactone with anticancer activity inhibits the proliferation of MDA-MB-231 MDA-MB-468 and MCF-7 human breast cancer cells (IC50s 5.211 3.405 and 9.083 UM respectively after 48 hours) inhibits migration of MDA-MB-231 cells at 2.5 5 and 10 UM reduces tumor volume in an MDA-MB-231 orthotopic mouse xenograft model at 25 and 50 mg/kg
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A G protein-biased peptide agonist of GLP-1R selectively induces cAMP accumulation in HEK293 cells expressing human GLP-1R overBarrestin recruitment in CHO-K1 cells expressing human GLP-1R (EC50s 0.63 and 79 nM respectively) induces insulin secretion in INS-1 832/3 cells (EC50 6.3 nM) reduces food intake and body weight increases plasma insulin levels and decreases plasma glucose HbA1c glucagon and triglyceride levels in diabetic db/db mice from 1.5-6 nmol/kg
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A peptide agonist of CaSR selective for CaSR over a panel of 33 receptors and ion channels as well as the norepinephrine transporter at 10 UM increases intracellular calcium levels in HEK293T cells expressing the human CaSR receptor (EC50 0 53 UM) inhibits parathyroid secretion from primary rat parathyroid cells (EC50 0 36 UM in the presence of calcium) decreases parathyroid hormone and calcium in plasma and serum respectively in a model of chronic renal insufficiency with secondary hyperthyroidism in nephrectomized rats fed high-phosphorus diet at 0 3 1 and 3 mg/kg
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A cell-permeable benzoxazolo-sulfonamide compound that blocks human FBPase-1 enzymatic activity by competing at the AMP allosteric binding site (IC50 3 4 UM Ki 1 1 UM) blocks glucose production in starved rat hepatoma cells (IC50 6 6 UM)
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A DNA alkylating agent active metabolite of dacarbazine (DTIC) active degradation product of temozolomide cytotoxic to L-cells and decreases thymidine and uridine uptake by 55 and 65 respectively at 1 mM cytotoxic to TLX5 murine lymphoma cells induces formation of mammary adenofibromas in rats when administered at a cumulative dose of 890 mg per animal over 14 weeks
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The primary PGD2 metabolite formed from PGD2 via PGFS in the liver or lung induces contraction of isolated cat iris sphincter (EC50 0 045 UM) induces contraction of isolated human bronchial smooth muscle from 0 1-30 UM induces ERK and CREB phosphorylation as well as increases the viability of MCF-7 breast cancer cells stably expressing the FP receptor at 0 1 and 1 UM
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