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Product Image-630-3169

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.

Product Image-113-9225

Bouffant caps, PP

Supplier: HUBEI ORIENT INTL TRADING
Description: Disposable bouffant caps made from non woven PP. Ideal for use in non hazardous environments.

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
Product Image-HOIT110694

Overalls without hood or feet cover, PP

Supplier: HUBEI ORIENT INTL TRADING
Description: These disposable overalls are made from non woven PP. Ideal for non critical applications in industrial, clinical or food processing environments.

Image Unavailable-BOSSBS-7974R-CY7

Anti-ATXN2 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-7974R-CY7)
Supplier: Bioss
Description: The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ATX2 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. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
UOM: 1 * 100 µl
Image Unavailable-MILLZAFS0160GE

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-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
Image Unavailable-LIOF402040

Media in bottles, sabouraud dextrose broth

Catalog Number: (LIOF402040)
Supplier: LIOFILCHEM
Description: Sabouraud dextrose broth (SDB) is a liquid medium used in qualitative procedures for isolation of yeasts and moulds and for the culture or subculture of fungi from clinical and nonclinical specimens.
UOM: 1 * 1 items

Certificates


Product Image-113-9219

Bouffant caps, PP

Supplier: HUBEI ORIENT INTL TRADING
Description: Disposable bouffant caps made from non woven PP. Ideal for use in non hazardous environments.

Image Unavailable-BOSSBS-4807R-A488

Anti-ATXN3L Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalog Number: (BOSSBS-4807R-A488)
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-CY7

Anti-ATXN3L Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-4807R-CY7)
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

Anti-ATXN3L Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-4807R)
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-A680

Anti-ATXN3L Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-4807R-A680)
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
Product Image-113-8322

VWR®, Isolation Gowns

Supplier: VWR Collection
Description: These disposable gowns, with back fastening, are made of non woven, breathable SMS fabric. Ideal for use in healthcare environments and hospitals.

Product Image-HOIT4021W52BDAC3XL

Overalls with hood and without feet cover, PP

Supplier: HUBEI ORIENT INTL TRADING
Description: These disposable overalls are made from non woven PP. Ideal for non critical applications in industrial, clinical or food processing environments.

Product Image-GOJO9663-12

PURELL® Advanced Hygienic Hand Rub Bottles

Supplier: GOJO Industries - Europe Ltd
Description: A no-rinse hygienic hand rub that feels great to use and is clinically proven to maintain skin health.

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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 +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at +43 1 97002 - 0.
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