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cis-\u200BEthyl+4-\u200Baminocyclohexanecarb\u200Boxylate+HCl+sal
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cis-\u200BEthyl+4-\u200Baminocyclohexanecarb\u200Boxylate+HCl+sal
Catalog Number:
(10282-056)
Supplier:
Bioss
Description:
ADH6 (alcohol dehydrogenase 6), also known as ADH-5, is a 368 amino acid member of the class V zinc-containing alcohol dehydrogenase family. This family of enzymes functions to metabolize a wide variety of substrates such as retinol, hydroxysteroids, ethanol, aliphatic alcohols and lipid peroxidation products. Localized to the cytoplasm and expressed in the stomach and liver, ADH6 catalyzes the reversible oxidation of alcohols to their corresponding aldehydes or ketones and is able to bind two zinc ions as cofactors. ADH6 contains a glucocorticoid response element upstream of its 5' UTR which is thought to be a steroid binding site, suggesting that expression of ADH6 may be under hormonal control. Multiple isoforms of ADH6 exist due to alternative splicing events.
Catalog Number:
(80055-138)
Supplier:
MilliporeSigma
Description:
A cell-permeable inhibitor of protein phosphatase 2A (PP2A; IC50=0.5–1.0nM) and protein phosphatase 1 (PP1; IC50=2nM)
Catalog Number:
(10282-026)
Supplier:
Bioss
Description:
The alcohol dehydrogenase family of proteins metabolize a wide variety of substrates, including retinol, hydroxysteroids, ethanol, aliphatic alcohols and lipid peroxidation products. ADH5 (alcohol dehydrogenase 5 (class III)), also known as FDH (formaldehyde dehydrogenase), ADHX, ADH-3 or GSNOR, is a 374 amino acid cytoplasmic protein that belongs to the class III subfamily of alcohol dehydrogenases. Expressed ubiquitously, ADH5 uses iron as a cofactor to catalytically oxidize both long-chain primary alcohols and S-hydroxymethyl-glutathione, a product formed spontaneously between formaldehyde and glutathione. ADH5 exists as a homodimer and, via its ability to oxidize S-hydroxymethyl-glutathione and, thus, eliminate formaldehyde, functions as an important component of cellular metabolism. Genetic variations in the gene encoding ADH5 may affect drug and alcohol dependence in humans.
Supplier:
Adipogen
Description:
Anticancer compound. Orally active, potent and selective colony stimulating factor 1 receptor (CSF-1R; c-Fms) inhibitor. More than 1000-fold selective against its closest receptor tyrosine kinase homologs c-KIT and platelet-derived growth factor receptor beta (PDGFRbeta). Selective against more than 200 additional kinases.
Supplier:
Honeywell Research Chemicals
Description:
Original and Innovative Karl Fischer Reagents to analyze or measure water content
Supplier:
TCI America
Description:
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-fluoro-L-phenylalanine, Purity: >95.0%(HPLC)(T), CAS No: 169243-86-1, MF: C24H20FNO4, MW: 405.43, Synonym: N-Fmoc-4-fluoro-L-phenylalanine, Fmoc-Phe(4-F)-OH, Form: Crystal- Powder, Size: 1G
Supplier:
MilliporeSigma
Description:
Precursor for prostaglandins, prostacyclin and thromboxane
Supplier:
Adipogen
Description:
Potential sensitive probe. Determination of plasma membrane potential of neutrophils generated by the Na+ pump.
Catalog Number:
(80056-972)
Supplier:
Adipogen
Description:
TG100115 inhibits PI3Kgamma and delta, with IC(50) values of 83 and 235nM, respectively.
Supplier:
Adipogen
Description:
Fluorescent substrate for oxidoreductases, especially for Cytochrome P450.
Supplier:
Agilent Technologies
Description:
The GeneJammer transfection reagent is a proprietary formulation of novel polyamines ideal for transient or stable transfections in a wide variety of cell types.
Supplier:
Restek
Description:
The Restek PFP Propyl is a great choice for the retention and selectivity of charged bases, electronegative compounds, and amine-containing compounds.
Supplier:
Spectrum Chemicals
Description:
2,2,2-Tribromoethanol, Purity: 98%, Cas number: 75-80-9, Molecular Formula: C2H3Br3O, Molecular Weight: 282.76, Color/Form: White, Pale yellow crystal powder, Size: 100GM
Supplier:
Adipogen
Description:
Fumitremorgin-type alkaloid. Tremorgenic neurotoxic mycotoxin. Selective blocker of KCa1.1 (high-conductance Ca2+-activated K+; BK; maxi-K) channels. Decreases GABA levels in CNS. Increases spontaneous glutamate and aspartate release. At toxic doses, increases the number and decreases the affinity of DHP receptors in rat cortex. Cell cycle inhibitor at the M phase. Inhibits calmodulin and PKC activity. Has apoptotic effects on human T lymphocytes. Stimulates the growth of seedling roots of buckwheat.
Supplier:
Electron Microscopy Sciences
Description:
A water soluble embedding media which is based on Glycol Methacrylate (GMA) plastic embedding. It is intended for use in preparing samples for high resolution microscopes (HRLM). The catalyzed monomer acts as a dehydration and infiltration agent. Therefore, complete dehydration through 100% ethanol is not necessary although recommended for large or dense tissues. Conventional paraffin sections have a greater degree of shrinkage and produce inadequate morphology when compared to JB-4.JB-4 Kit Consists of 800 mL Solution A, 30 mL Solution B, and 12 g Catalyst.
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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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