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Supplier: PerkinElmer
Description: Soft carrying case

Supplier: Thermo Scientific
Description: O₂ gas regulator, 2-stage for gas tank, For: Heracell VIOS 160i, 250i

Supplier: JUSTRITE MANUFACTURING
Description: Lecture Bottle (LB) Gas Cylinder Holder provides safety when moving and storing of gas cylinders.

Catalog Number: (HEWLRMSA-2)
Supplier: Agilent
Description: Big universal trap (Ar), ⅛" fittings, For: GC, GC/MS
UOM: 1 * 1 items


Catalog Number: (NEUB0578-60-121414)
Supplier: NEUBERT VOLUME GLASSWAERE
Description: Components individually, from Boro 3.3; inserts with safety glass ring.
UOM: 1 * 1 items


Supplier: Abcam
Description: Anti-Galectin 3+Galectin 1+Galectin 8 Rabbit Recombinant Multiclonal Antibody [clone: RM1261]

New Product

Catalog Number: (PEAK3304532)
Supplier: PEAK SCIENTIFIC
Description: Bringing Single Quad LC-MS users the very latest in nitrogen gas generator technology, Horizen 24 is the culmination of over 25 years at the forefront of nitrogen gas generation for the laboratory.
UOM:

New Product


Supplier: Agilent
Description: Removable needle, gas tight, 2500 μl, For: ASI-100

Supplier: UVP ULTRA VIOLET PRODUCTS
Description: Spectrum lamp, Rare gas, Pen-Ray®, Xenon lamp

Catalog Number: (ANTIA78133-96)
Supplier: ANTIBODIES.COM
Description: Mouse GAS 6 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the <i>in vitro</i> quantitative determination of mouse GAS 6 in serum, plasma, tissue homogenates, and other biological fluids.
UOM: 1 * 96 Tests

New Product


Catalog Number: (514-0007)
Supplier: 3M
Description: Monitor uses the proven scientific principle of diffusion which involves the gradual mixing of molecules of two or more substances for measuring personal exposure in work areas of industries.
UOM: 1 * 5 items


Catalog Number: (BOSSBS-13312R-A555)
Supplier: Bioss
Description: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13312R-CY7)
Supplier: Bioss
Description: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13312R-A350)
Supplier: Bioss
Description: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-11307R-HRP)
Supplier: Bioss
Description: Cyclooxygenases metabolize arachidonate to five primary prostanoids: PGE2, PGF2?, PGI2, TXA2 and PGD2. These lipid mediators interact with specific members of G protein-coupled prostanoid receptors, designated EP, FP, IP, TP and DP, respectively. The IP Receptor binds prostacyclin, PGI2, the main pro-stanoid synthesized by vascular tissues.Upon binding to the IP Receptor, prostacyclin activates adenylate cyclase primarily through the Gas protein. The gene encoding the human IP Receptor is located on chromosome 19. It is expressed as a glycosylated and phosphorylated protein, which is abundantly expressed in vascular tissues such as aorta, lung, atrium and ventricle, as well as in kidney, thymus, spleen and neurons.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-11307R-FITC)
Supplier: Bioss
Description: Cyclooxygenases metabolize arachidonate to five primary prostanoids: PGE2, PGF2?, PGI2, TXA2 and PGD2. These lipid mediators interact with specific members of G protein-coupled prostanoid receptors, designated EP, FP, IP, TP and DP, respectively. The IP Receptor binds prostacyclin, PGI2, the main pro-stanoid synthesized by vascular tissues.Upon binding to the IP Receptor, prostacyclin activates adenylate cyclase primarily through the Gas protein. The gene encoding the human IP Receptor is located on chromosome 19. It is expressed as a glycosylated and phosphorylated protein, which is abundantly expressed in vascular tissues such as aorta, lung, atrium and ventricle, as well as in kidney, thymus, spleen and neurons.
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.
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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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