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Catalog Number: (H-062-1ML)
Supplier: Merck
Description: This stable-labeled internal standard is suitable for quantitation of hydroxybupropion levels in urine, serum, or plasma by LC/MS or GC/MS for urine drug testing, clinical toxicology, forensic analysis, or isotope dilution methods.
UOM: 1 * 1 mL


Supplier: Merck
Description: Used to stain blood, bone marrow smears, and clinical cytological specimens

MSDS Sale

Catalog Number: (ENZOBMLCM1120500)
Supplier: ENZO LIFE SCIENCES
Description: Clinically useful diuretic. Clopamide selectively inhibits the chloride the sodium chloride cotransporter.
UOM: 1 * 500 mg


Catalog Number: (1.01350.1000)
Supplier: Merck
Description: Used to stain blood, bone marrow smears, and clinical cytological specimens.
UOM: 1 * 1 kg

MSDS


Catalog Number: (V-009-1ML)
Supplier: Merck
Description: 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


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

Supplier: VWR Collection
Description: The safety bottle carrier provides a safe and reliable way to transport a variety of bottled reagents in the lab. Available in 1,5 and 4,5 L capacities, this carrier is the practical answer for any clinical and research lab setting.

Catalog Number: (V-027-1ML)
Supplier: Merck
Description: 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


Catalog Number: (ENZOBMLNA1390001)
Supplier: ENZO LIFE SCIENCES
Description: Sodium channel blocker. Clinically useful local anesthetic.
UOM: 1 * 1 g


Catalog Number: (LIOF26490)
Supplier: LIOFILCHEM
Description: VTM is suitable for collection and preservation of clinical specimens containing viruses, including SARS-CoV-2 (COVID-19), Chlamydia spp., Mycoplasma spp. and Ureaplasma spp.
UOM: 1 * 100 items

Catalog Number: (LIOF96147)
Supplier: LIOFILCHEM
Description: Identification of the main pathogenic microorganisms directly from clinical specimens.
UOM: 1 * 1 items


Catalog Number: (ICNA091003122)
Supplier: MP Biomedicals
Description: Basal Medium Eagle is suited for the isolation and cultivation of non-fastidious and fastidious microorganisms from a variety of clinical and non-clinical specimens. It can also be used as a selective isolation medium by adding antimicrobial agents.
UOM: 1 * 10 L


Catalog Number: (BOSSBS-4807R-A750)
Supplier: Bioss
Description: 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


Catalog Number: (BOSSBS-4807R-HRP)
Supplier: Bioss
Description: 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


Supplier: Merck
Description: For staining of blood and bone marrow smears and clinical-cytological specimens
Supplier: HIRSCHMANN
Description: Closure caps

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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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