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4-Hydroxycinnamic+acid
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4-Hydroxycinnamic+acid
Catalog Number:
(RC698.3-16)
Supplier:
Honeywell Research Chemicals
Description:
BioSyn products are ideal for DNA, RNA and oligonucleotide synthesis. All solvents and regents are filtered (0.2-micron) and tested for oxidation reage.
Supplier:
BeanTown Chemical
Description:
CAS: 13446-49-6; EC No: 236-599-2; MDL No: MFCD00011370
Powder; Molecular Formula: K2MoO4; MW: 238.14
Melting Point: 919°
Density (g/mL): 2.3
Hygroscopic
Supplier:
Transene
Description:
Tantalum Etchant 111 provides controlled etching of tantalum, tantalum oxide, and tantalum nitride materials.
Supplier:
AMBEED, INC
Description:
Minoxidil 95%
Supplier:
TLC PHARMACEUTICAL STANDARD LTD
Description:
Pharmaceutical Standards, Escitalopram EP Impurity H HCl (Citalopram USP Related Compound E, Citalopram N-Oxide HCl)
Supplier:
MP Biomedicals
Description:
Potassium Iodide is known as Potassium Salt of Hydriodic Acid [HI], available in white crystalline powder form. It is a mild reducing agent and can be easily oxidized to Iodine by powerful oxidizing agent like chlorine. With elemental iodine it forms I3 (tri iodide), the salts of tri iodide are highly water soluble.
Readily soluble in water.
Catalog Number:
(10452-852)
Supplier:
Bioss
Description:
Uricase catalyzes the oxidation of uric acid to 5 hydroxyisourate which spontaneously decomposes to form allantoin.
Catalog Number:
(76101-546)
Supplier:
Bioss
Description:
Receptor that mediates the recognition, internalization and degradation of oxidatively modified low density lipoprotein (oxLDL) by vascular endothelial cells. OxLDL is a marker of atherosclerosis that induces vascular endothelial cell activation and dysfunction, resulting in pro-inflammatory responses, pro-oxidative conditions and apoptosis. Its association with oxLDL induces the activation of NF-kappa-B through an increased production of intracellular reactive oxygen and a variety of pro-atherogenic cellular responses including a reduction of nitric oxide (NO) release, monocyte adhesion and apoptosis. In addition to binding oxLDL, it acts as a receptor for the HSP70 protein involved in antigen cross-presentation to naive T-cells in dendritic cells, thereby participating in cell-mediated antigen cross-presentation. Also involved in inflammatory process, by acting as a leukocyte-adhesion molecule at the vascular interface in endotoxin-induced inflammation. Also acts as a receptor for advanced glycation end (AGE) products, activated platelets, monocytes, apoptotic cells and both Gram-negative and Gram-positive bacteria (By similarity).
Catalog Number:
(80050-000)
Supplier:
MilliporeSigma
Description:
A selective, irreversible, slow, tight-binding inhibitor of inducible nitric oxide synthase (iNOS; Kd=7nM) both in vitro and in vivo
Catalog Number:
(80052-584)
Supplier:
MilliporeSigma
Description:
Potent stimulator of bone resorption and stimulator of nuclear phospholipase C. Induces nitric oxide synthase. Biological Activity: ED50=3–10pg/mL as measured in a cell proliferation assay.
Catalog Number:
(89151-150)
Supplier:
Enzo Life Sciences
Description:
Most efficient spin trap for the <i>in vitro</i> and<i> in vivo</i> detection of O-, N-, S-, and C-centered free radicals.
Catalog Number:
(10336-432)
Supplier:
Bioss
Description:
Produces nitric oxide (NO) which is a messenger molecule with diverse functions throughout the body. In macrophages, NO mediates tumoricidal and bactericidal actions. Also has nitrosylase activity and mediates cysteine S-nitrosylation of cytoplasmic target proteins such COX2.
Catalog Number:
(10102-530)
Supplier:
Prosci
Description:
DHODH catalyzes the fourth enzymatic step, the ubiquinone-mediated oxidation of dihydroorotate to orotate, in de novo pyrimidine biosynthesis. It is a mitochondrial protein located on the outer surface of the inner mitochondrial membrane.The protein encoded by this gene catalyzes the fourth enzymatic step, the ubiquinone-mediated oxidation of dihydroorotate to orotate, in de novo pyrimidine biosynthesis. This protein is a mitochondrial protein located on the outer surface of the inner mitochondrial membrane. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Catalog Number:
(10108-680)
Supplier:
Prosci
Description:
ABP1 is a membrane glycoprotein that is expressed in many epithelium-rich and/or hematopoietic tissues and oxidatively deaminates putrescine and histamine. The protein may play a role in controlling the level of histamine and/or putrescine in these tissues. It also binds to and is inhibited by amiloride, a diuretic that acts by closing epithelial sodium ion channels.This gene encodes a membrane glycoprotein that is expressed in many epithelium-rich and/or hematopoietic tissues and oxidatively deaminates putrescine and histamine. The protein may play a role in controlling the level of histamine and/or putrescine in these tissues. It also binds to and is inhibited by amiloride, a diuretic that acts by closing epithelial sodium ion channels.
Catalog Number:
(10102-814)
Supplier:
Prosci
Description:
SLC25A20 is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space.It mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants.This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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