You Searched For: Curcumin


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Supplier: Cayman Chemical
Description: Curcumin

Supplier: Apollo Scientific
Description: Curcumin 97%

Supplier: Apollo Scientific
Description: Curcumin 98%

Supplier: Thermo Fisher Scientific
Description: Curcumin 98+% (mixture of Curcumin, demethoxyCurcumin, and bisdemethoxyCurcumin)
Catalog Number: (APOSBICL4054-1MG)
Supplier: Apollo Scientific
Description: Curcumin-4-O-β-D-glucuronide ≥85%
UOM: 1 * 1 mg


Supplier: Thermo Fisher Scientific
Description: Curcumin 95% (total Curcuminoid content)
Supplier: ENZO LIFE SCIENCES
Description: Curcumin (from Curcuma longa) ≥98% (by HPLC), high purity

Catalog Number: (EHERC11780000)
Supplier: EHRENSTORFER
Description: Curcumin
UOM: 1 * 0,25 g


Catalog Number: (ROTH9469.1)
Supplier: Roth Carl
Description: Curcumin
UOM: 1 * 10 g


Supplier: Merck
Description: Curcumin, Sigma-Aldrich®

Catalog Number: (1151855.)
Supplier: USP
Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
UOM: 1 * 30 mg


Catalog Number: (MOLEM17132282)
Supplier: Molekula
Description: Curcumin
UOM: 1 * 10 g


Catalog Number: (SIALC7727-500MG)
Supplier: Merck
Description: Curcumin, Sigma-Aldrich®
UOM: 1 * 500 mg

Catalog Number: (BOSSBS-7115R-CY5)
Supplier: Bioss
Description: MLC1 is a 377 amino acid multi-pass membrane protein that may serve as a non-selective neuronal cation channel in brain. Mutant MLC1 proteins that show impaired folding have been corrected in vitro with the addition of a Ca(2+)-ATPase inhibitor, curcumin. Mutations in the gene encoding MLC1 is the cause of megalencephalic leukoencephalopathy with subcortical cysts, also known as van der Knaap disease, a rare syndrome characterized early in life by progressive brain destruction causing mental retardation and incoordination. Single nucleotide polymorphisms within the MLC1 gene may be associated with periodic catatonia, but there seems to be conflicting evidence on whether or not the gene is implicated in general schizophrenia.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-8111R)
Supplier: Bioss
Description: CCDC116 is a 515 amino acid protein that exists as two alternatively spliced isoforms. Encoded by a gene that maps to human chromosome 22q11.21, CCDC116 is induced by curcumin (diferulolylmethane), although its role is unclear. CCDC116 is significantly affected by dietary curcumin, which may have a protective role in inflammatory bowel disease (IBD) and may reduce the relapse rate in human ulcerative colitis (UC). As the second smallest human chromosome, chromosome 22 contains over 500 genes and about 49 million bases. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocation between chromosomes 9 and 22 may lead to the formation of Philadelphia Chromosome and subsequent production of a novel fusion protein known as BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-7115R-A750)
Supplier: Bioss
Description: MLC1 is a 377 amino acid multi-pass membrane protein that may serve as a non-selective neuronal cation channel in brain. Mutant MLC1 proteins that show impaired folding have been corrected <i>in vitro</i> with the addition of a Ca(2+)-ATPase inhibitor, curcumin. Mutations in the gene encoding MLC1 is the cause of megalencephalic leukoencephalopathy with subcortical cysts, also known as van der Knaap disease, a rare syndrome characterised early in life by progressive brain destruction causing mental retardation and incoordination. Single nucleotide polymorphisms within the MLC1 gene may be associated with periodic catatonia, but there seems to be conflicting evidence on whether or not the gene is implicated in general schizophrenia.
UOM: 1 * 100 µl


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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 call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
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 call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at +43 1 97002 - 0.
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