You Searched For: DETA+NONOate+(NOC-18)


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Supplier: ENZO LIFE SCIENCES
Description: Nitric oxide (NO) donor.

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Supplier: Thermo Scientific
Description: CAS No.: 146724-94-9

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Supplier: ENZO LIFE SCIENCES
Description: Nitric oxide (NO) donor.

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Supplier: ENZO LIFE SCIENCES
Description: Nitric oxide (NO) donor.

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Supplier: ENZO LIFE SCIENCES
Description: DEA NONOate is used as a nitric oxide donor.

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Catalog Number: (ENZOALX430067M005)
Supplier: ENZO LIFE SCIENCES
Description: Negative control for NO releasing NONOates.
UOM: 1 * 5 mg

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Supplier: Cayman Chemical
Description: DEA NONOate is a NO donor. It spontaneously dissociates in a pH-dependent, first-order process with a half-life of 2 minutes and 16 minutes at 37 °C and 22 to 25 °C, pH 7.4, respectively, to liberate 1.5 moles of NO per mole of parent compound.

Supplier: ENZO LIFE SCIENCES
Description: Nitric oxide (NO) donor.

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Supplier: ENZO LIFE SCIENCES
Description: Nitric oxide (NO) donor.

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Supplier: ENZO LIFE SCIENCES
Description: Nitric oxide (NO) donor.

New Product

Supplier: ENZO LIFE SCIENCES
Description: Nitric oxide (NO) donor.

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Supplier: ENZO LIFE SCIENCES
Description: Nitric oxide (NO) donor.

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Supplier: Spectrum Chemical
Description: Diethylenetriamine is also known under the abbreviation DETA and is a colorless liquid that is hygroscopic and soluble in both water and polar organic solvents. Used as a ligand forming complex in coordination chemistry, it is also used for the extraction of gases that are acid in the oil industry.

Catalog Number: (BOSSBS-13587R-A680)
Supplier: Bioss
Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13587R-A750)
Supplier: Bioss
Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13587R-A488)
Supplier: Bioss
Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
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 on +353 1 88 22222.
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 eurega_services@eu.vwr.com
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