You Searched For: Uridine-5\'-triphosphoric+acid+trisodium+salt+(UTP-Na3)+dihydrate


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Supplier: Thermo Fisher Scientific
Description: Sodium dihydrogen phosphate dihydrate 98%, Extra Pure
Catalog Number: (PROOBP459)
Supplier: LGC Standards PROMOCHEM
Description: Riboflavine-5'-phosphate sodium salt
UOM: 1 * 50 mg

Catalog Number: (BOSSBS-13007R-A680)
Supplier: Bioss
Description: Dyskerin (NAP57) associates with the chaperone protein Nopp140 and forms a small ribonucleoprotein particle with GAR1 (NOLA1), NHP2 (NOLA2) and Nop10 for the isomerization of uridine to pseudouridine (1). GAR1, NHP2 and dyskerin localize to the dense fibrillar component of the nucleolus and in nuclear Cajal bodies (2). The dyskerin gene maps to chromosome Xq28 (3). Missense mutations in the dyskerin gene interfere with normal nuclear localization of dyskerin and cause Dyskeratosis congenita (DKC) (4). DKC is a rare, X-linked bone marrow disorder characterized by cutaneous hyperpigmentation, dystrophy of the nails, atrophy of the testicles and leukoplakia of the oral mucosa. The GAR1 gene maps to chromosome 4q25 (5,6). The NHP2 gene maps to chromosome 5q35.3 and encodes a 155-amino acid protein (2,7).
UOM: 1 * 100 µl


Supplier: Thermo Fisher Scientific
Description: Quinine sulphate dihydrate, meets analytical specification of USP
Catalog Number: (BOSSBS-13007R-A750)
Supplier: Bioss
Description: Dyskerin (NAP57) associates with the chaperone protein Nopp140 and forms a small ribonucleoprotein particle with GAR1 (NOLA1), NHP2 (NOLA2) and Nop10 for the isomerization of uridine to pseudouridine (1). GAR1, NHP2 and dyskerin localize to the dense fibrillar component of the nucleolus and in nuclear Cajal bodies (2). The dyskerin gene maps to chromosome Xq28 (3). Missense mutations in the dyskerin gene interfere with normal nuclear localization of dyskerin and cause Dyskeratosis congenita (DKC) (4). DKC is a rare, X-linked bone marrow disorder characterized by cutaneous hyperpigmentation, dystrophy of the nails, atrophy of the testicles and leukoplakia of the oral mucosa. The GAR1 gene maps to chromosome 4q25 (5,6). The NHP2 gene maps to chromosome 5q35.3 and encodes a 155-amino acid protein (2,7).
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13007R-A647)
Supplier: Bioss
Description: Dyskerin (NAP57) associates with the chaperone protein Nopp140 and forms a small ribonucleoprotein particle with GAR1 (NOLA1), NHP2 (NOLA2) and Nop10 for the isomerization of uridine to pseudouridine (1). GAR1, NHP2 and dyskerin localize to the dense fibrillar component of the nucleolus and in nuclear Cajal bodies (2). The dyskerin gene maps to chromosome Xq28 (3). Missense mutations in the dyskerin gene interfere with normal nuclear localization of dyskerin and cause Dyskeratosis congenita (DKC) (4). DKC is a rare, X-linked bone marrow disorder characterized by cutaneous hyperpigmentation, dystrophy of the nails, atrophy of the testicles and leukoplakia of the oral mucosa. The GAR1 gene maps to chromosome 4q25 (5,6). The NHP2 gene maps to chromosome 5q35.3 and encodes a 155-amino acid protein (2,7).
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13007R-A555)
Supplier: Bioss
Description: Dyskerin (NAP57) associates with the chaperone protein Nopp140 and forms a small ribonucleoprotein particle with GAR1 (NOLA1), NHP2 (NOLA2) and Nop10 for the isomerization of uridine to pseudouridine (1). GAR1, NHP2 and dyskerin localize to the dense fibrillar component of the nucleolus and in nuclear Cajal bodies (2). The dyskerin gene maps to chromosome Xq28 (3). Missense mutations in the dyskerin gene interfere with normal nuclear localization of dyskerin and cause Dyskeratosis congenita (DKC) (4). DKC is a rare, X-linked bone marrow disorder characterized by cutaneous hyperpigmentation, dystrophy of the nails, atrophy of the testicles and leukoplakia of the oral mucosa. The GAR1 gene maps to chromosome 4q25 (5,6). The NHP2 gene maps to chromosome 5q35.3 and encodes a 155-amino acid protein (2,7).
UOM: 1 * 100 µl


Catalog Number: (APOSBIP0705-25G)
Supplier: Apollo Scientific
Description: Biological buffer - useful range 7.2-8.5
UOM: 1 * 25 g


Catalog Number: (BOSSBS-4180R-A350)
Supplier: Bioss
Description: Receptor for ATP and UTP coupled to G-proteins that activate a phosphatidylinositol-calcium second messenger system. The affinity range is UTP = ATP >ATP-gamma-S >2-methylthio-ATP = ADP.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-4180R-A555)
Supplier: Bioss
Description: Receptor for ATP and UTP coupled to G-proteins that activate a phosphatidylinositol-calcium second messenger system. The affinity range is UTP = ATP >ATP-gamma-S >2-methylthio-ATP = ADP.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-4180R-A680)
Supplier: Bioss
Description: Receptor for ATP and UTP coupled to G-proteins that activate a phosphatidylinositol-calcium second messenger system. The affinity range is UTP = ATP > ATP-gamma-S >> 2-methylthio-ATP = ADP.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-4180R-HRP)
Supplier: Bioss
Description: Receptor for ATP and UTP coupled to G-proteins that activate a phosphatidylinositol-calcium second messenger system. The affinity range is UTP = ATP >ATP-gamma-S >2-methylthio-ATP = ADP.
UOM: 1 * 100 µl


Supplier: Apollo Scientific
Description: Uridine 99%

Supplier: Thermo Fisher Scientific
Description: Uridine ≥99%
Catalog Number: (A0666.0025)
Supplier: PanReac AppliChem
Description: Uridine
UOM: 1 * 25 g


Supplier: Apollo Scientific
Description: Uridine 99%

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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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The original product is no longer available. The replacement shown is available.
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