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Image Unavailable-ENZOBMLEI1630005

Meclofenamic acid sodium salt ≥98% (by HPLC)

Catalog Number: (ENZOBMLEI1630005)
Supplier: ENZO LIFE SCIENCES
Description: 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


Image Unavailable-ICNA091003122

Cell culture media, powdered, Basal Medium Eagle (BME) Modified, MP Biomedicals

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

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Product Image-LIOF26490

VTM - virus transport medium

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

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Image Unavailable-BOSSBS-4807R-A750

Anti-ATXN3L Rabbit Polyclonal Antibody (Alexa Fluor® 750)

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
Image Unavailable-BOSSBS-4807R-HRP

Anti-ATXN3L Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

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
Product Image-631-1075

VWR® Q Path® Slide Holders

Supplier: VWR Collection
Description: Slide holders designed for applications in clinical cytology.

Product Image-113-9049

VWR®, Isolation Gowns

Supplier: VWR Collection
Description: These disposable gowns, with back fastening, are made of non woven PP.

Product Image-113-9410

VWR®, Cleanroom Socks, ESD, Disposable

Supplier: VWR Collection
Description: These disposable socks are made of polyester filament yarn and anti-static carbon fibre.

Environmentally Preferable Sale

Image Unavailable-1.09203.0100

Giemsa's stain for microscopy, Sigma-Aldrich®

Supplier: Merck
Description: Giemsa's staining is one of the standard procedures in histology, hematology, cytology and bacteriology. The Giemsa's azur-eosin-methylene blue dye is a dry dye that is used for the preparation of a staining solution. This solution can be used for the staining of blood and bone marrow smears, paraffin sections, spirochaets and clinical-cytological specimens of human origin.

MSDS

Image Unavailable-MILLZAFS0240UK

Water purification systems, AFS® 8/16/24

Supplier: Merck
Description: Economical water system, producing CLRW (Clinical Laboratory Reagent Water) quality with a dispensing flow rate to analyser up to 2 l/min. For clinical analysers with pure water needs up to 480 L daily

Image Unavailable-BOSSBS-4807R-A350

Anti-ATXN3L Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalog Number: (BOSSBS-4807R-A350)
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
Image Unavailable-BOSSBS-4807R-A555

Anti-ATXN3L Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-4807R-A555)
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
Image Unavailable-BOSSBS-4807R-CY5.5

Anti-ATXN3L Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-4807R-CY5.5)
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
Image Unavailable-BOSSBS-4807R-CY5

Anti-ATXN3L Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-4807R-CY5)
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
Image Unavailable-BOSSBS-4807R-FITC

Anti-ATXN3L Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-4807R-FITC)
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
Product Image-630-3168

Upright microscopes, DM 1000 LED

Supplier: LEICA MICROSYSTEMS
Description: The DM1000 LED laboratory microscope is perfect for clinical laboratory applications; histology, cytology, haematology and pathology.

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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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