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Catalogus nummer: (V-009-1ML)
Leverancier: Merck
Omschrijving: A new internal standard suitable for many LC/MS and GC/MS applications from forensic or clinical toxicology analysis to urine drug testing and isotope dilution methods. 
UOM: 1 * 1 mL


Catalogus nummer: (BOSSBS-10044R-A750)
Leverancier: Bioss
Omschrijving: NDV is a contagious and fatal viral disease affecting most species of birds. Clinical signs are extremely variable depending on the strain of virus, species and age of bird, concurrent disease, and preexisting immunity. Four broad clinical syndromes are recognised by scientists. They are Viscerotropic velogenic, Neurotropic velogenic, Mesogenic, and Lentogenic. NDV is so virulent that many birds die without showing any clinical signs. A death rate of almost 100 percent can occur in unvaccinated poultry flocks. NDV can infect and cause death even in vaccinated poultry. Fortunately NDV has not infected domestic chicken flocks in the United States since the last outbreak was eradicated in 1974.
UOM: 1 * 100 µl


Leverancier: Hubei Orient International
Omschrijving: These non woven shoe covers are made of PP with a skid-resistant CPE coating on the sole.

Catalogus nummer: (ENZOBMLCM1120500)
Leverancier: ENZO LIFE SCIENCES
Omschrijving: Clinically useful diuretic. Clopamide selectively inhibits the chloride the sodium chloride cotransporter.
UOM: 1 * 500 mg

New Product


Catalogus nummer: (V-027-1ML)
Leverancier: Merck
Omschrijving: A certified reference solution suitable for use as an internal standard for quantitation of O-desmethylvenlafaxine levels in urine or isotope dilution methods by LC/MS or GC/MS for clinical toxicology, urine drug testing, or forensic analysis.
UOM: 1 * 1 mL


Catalogus nummer: (114-9707)
Leverancier: VWR Collection
Omschrijving: VWR® Disposable cleanroom socks are designed to provide all day comfort inside a cleanroom. They are made from materials that prevent any particle generation while in use.
UOM: 1 * 400 PAAR


Catalogus nummer: (BOSSBS-4807R-HRP)
Leverancier: Bioss
Omschrijving: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-4807R-A750)
Leverancier: Bioss
Omschrijving: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterised by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
UOM: 1 * 100 µl


Leverancier: THERMO FISHER DIAGNOSTICS
Omschrijving: IMAGEN™ is a qualitative direct immunofluorescence test used for detection and confirmation of the presence of virus in cell culture or in clinical specimen.

Catalogus nummer: (ENZOBMLNS1120050)
Leverancier: ENZO LIFE SCIENCES
Omschrijving: Potent and selective serotonin uptake inhibitor (Ki=5.4nM). Modifies gene expression profile in Alzheimer lymphocytes. Clinically useful antidepressant.
UOM: 1 * 50 mg

New Product


Catalogus nummer: (ENZOBMLNA1390001)
Leverancier: ENZO LIFE SCIENCES
Omschrijving: Sodium channel blocker. Clinically useful local anesthetic.
UOM: 1 * 1 g

New Product


Leverancier: RATIOLAB
Omschrijving: All-purpose PE bags with self-adhesive strip for clinical and laboratory use.

Catalogus nummer: (ENZOBMLEI1630005)
Leverancier: ENZO LIFE SCIENCES
Omschrijving: Dual 5-lipoxygenase (IC50=46.8 µM) and cyclooxygenase I and II inhibitor (IC50=0.6 µM). Clinically useful NSAID.
UOM: 1 * 5 g

New Product


Catalogus nummer: (BOSSBS-4807R)
Leverancier: Bioss
Omschrijving: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-4807R-A680)
Leverancier: Bioss
Omschrijving: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterised by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
UOM: 1 * 100 µl


Leverancier: Thermo Scientific
Omschrijving: Whether clinical and diagnostic applications or cell culture and other research, now spin conical tubes, blood tubes and microplates all in one rotor at 7197xg in 4 L High Performance General Purpose Centrifuges.

Bel voor prijs
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.
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.
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 Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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