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Supplier: DISTRIBUTION RESULTS, INC.
Description: Highly absorbent, durable sponges for general laboratory cleaning.

Catalog Number: (470089-268)
Supplier: DISTRIBUTION RESULTS, INC.
Description: Sponges


Supplier: GILSON, INC.
Description: The best quality to guarantee repetitive distribution results

Product available on GSA Advantage®

Supplier: GILSON, INC.
Description: The best quality to guarantee repetitive distribution results.

Product available on GSA Advantage®

Supplier: Binder
Description: The BD Avantgarde.Line series is specially designed for gentle incubation of organisms, as well as conditioning of heatsensitive media. The design of the units and the homogeneous temperature distribution ensure the very best results.

Product available on GSA Advantage®

Catalog Number: (100501-314)
Supplier: Electron Microscopy Sciences
Description: EMS's Alumina Powders are accurately controlled for all specs and particle size distribution, assuring you the best polishing results.

Minority or Woman-Owned Business Enterprise


Catalog Number: (100501-324)
Supplier: Electron Microscopy Sciences
Description: EMS's Alumina Powders are accurately controlled for all specs and particle size distribution, assuring you the best polishing results.

Minority or Woman-Owned Business Enterprise


Catalog Number: (76554-226)
Supplier: ECOLAB LIFE SCIENCES
Description: Ecolab’s Klercide™ Triple Bucket System features a unique controlled application wringer which enables the even distribution of disinfectant over cleanroom surfaces. This enables accurate, repeatable results which help minimize operator error and enhance compliance with cGMP.


Catalog Number: (10109-444)
Supplier: Prosci
Description: Arginase catalyzes the hydrolysis of arginine to ornithine and urea. The type I isoform of ARG1, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.


Supplier: Caron Products
Description: Caron's Reach-in CO<sub>2</sub> Incubators are optimized for suspension and scale up cell culture applications that require agitation or shaking so nutrients are distributed throughout the culture media. Ready to accommodate shakers inside, these CO<sub>2</sub> incubators provide optimum environmental conditions for precise and reproducible results.

Environmentally Preferable Small Business Enterprise CSA Certified Product available on GSA Advantage®

Catalog Number: (CAPIPA5-18684)
Supplier: Thermo Scientific
Description: Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.


Catalog Number: (89359-924)
Supplier: Genetex
Description: Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.


Supplier: Restek
Description: All residual catalysts and low molecular weight fragments are removed from the MXT®-5 polymer, providing a tight mono-modal distribution and extremely low bleed.

Catalog Number: (10109-442)
Supplier: Prosci
Description: Arginase catalyzes the hydrolysis of arginine to ornithine and urea. The type I isoform of ARG1, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.


Catalog Number: (89416-978)
Supplier: Prosci
Description: FKBP15 Antibody: FKBP15, also known as FKBP133, is a member of the FK506-binding protein family, a group of proteins initially identified as immunophilins, targets for the immunosupressant drugs FK506 and Rapamycin. FKBP15 is expressed in the developing nervous system and contains a domain similar to Wiskott-Aldrich syndrome protein homology region 1 (WH1) in addition to the FK506-binding protein motif. FKBP15 is distributed along the axonal shafts and partially co-localizes with F-actin in the growth cones of dorsal root ganglion neurons; overexpression of FKBP15 resulted in the number of filopodia in transfected neurons, suggesting that FKBP15 modulates growth cone behavior. FKBP15 has also been shown to associate with both microtubules and the actin filament systems and disruption of its expression by RNAi resulted in delayed transport of early endosomes in HeLa cells indicating that FKBP15 is also involved in the transport of early endosomes. At least three isoforms of FKBP15 are known to exist.


Supplier: Electron Microscopy Sciences
Description: For accurate counting of blood cells platelets, dust/yeast cluster and specimen samples. Sharp contrast from rhodium plated on "V-Load". Triple dividing lines clearly delineate counting area for accurate and precise results. Molded from a single piece of thermal and shock resistant glass with a polished chamber and cover glass assuring precise capillary loading and even cell distribution. Fluid volume is 0.1 mm<sup>3</sup>/mm<sup>2</sup> and 0.00025 mm<sup>2</sup> per each square.

Minority or Woman-Owned Business Enterprise

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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 1-800-932-5000.
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