Du sökte efter: Curcumin

Leverantör: Merck

Beskrivning: Curcumin för syntes, Sigma-Aldrich®

Säkerhetsdatablad Certifikat

Leverantör: Apollo Scientific

Beskrivning: Curcumin 98%

Certifikat

Artikel nummer : (78246-100MG)

Leverantör: Merck

Beskrivning: Curcumin ≥99.5% matrix substance for MALDI-MS, Supelco®

UOM: 1 * 100 mg

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Artikel nummer : (APOSBICL4054-1MG)

Leverantör: Apollo Scientific

Beskrivning: Curcumin-4-O-β-D-glucuronide ≥85%

UOM: 1 * 1 mg

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Leverantör: ENZO LIFE SCIENCES AG

Beskrivning: Curcumin (from Curcuma longa) ≥98%, high purity

New Product

Leverantör: Cayman Chemical

Beskrivning: Curcumin

Leverantör: Apollo Scientific

Beskrivning: Curcumin 97%

Artikel nummer : (08511-10MG)

Leverantör: Merck

Beskrivning: Organic Standard, Curcumin

UOM: 1 * 10 mg

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Leverantör: Thermo Scientific

Beskrivning: Curcumin 98+% (mixture of Curcumin, demethoxyCurcumin, and bisdemethoxyCurcumin)

Säkerhetsdatablad Certifikat

Leverantör: TCI EUROPE

Beskrivning: Curcumin (naturliga)

Leverantör: TCI EUROPE

Beskrivning: Curcumin ≥97.0%

Leverantör: Thermo Scientific

Beskrivning: Curcumin 95%

Säkerhetsdatablad Certifikat

Artikel nummer : (1151855.)

Leverantör: USP

Beskrivning: 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

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Artikel nummer : (BOSSBS-7115R-CY7)

Leverantör: Bioss

Beskrivning: 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

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Artikel nummer : (BOSSBS-7115R)

Leverantör: Bioss

Beskrivning: 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

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Artikel nummer : (BOSSBS-7115R-CY5)

Leverantör: Bioss

Beskrivning: 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

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