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Product Image-MODU371213

Safety blood lancets, VITREX® STERILANCE® Lite III

Catalog Number: (MODU371213)
Supplier: Vitrex Medical A/S
Description: Safety lancets for blood glucose and other<i> in vitro</i> diagnostic tests.
UOM: 1 * 100 items
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-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
Product Image-HOIT109758

Mob caps, non woven PP

Catalog Number: (HOIT109758)
Supplier: HUBEI ORIENT INTL TRADING
Description: Disposable mob caps made from non woven PP.
UOM: 1 * 1.000 items
Product Image-EE222

Chromogenic media for colourful microbial detection, CHROMagar™

Supplier: CHROMAGAR
Description: Chromogenic technology applied to culture media allows you to differentiate and easily identify, inside one single plate, the growth of different microorganisms.

Image Unavailable-LIOF6100135

Dehydrated Culture Media, Columbia Agar Base

Catalog Number: (LIOF6100135)
Supplier: LIOFILCHEM
Description: Columbia agar base, enriched with sterile sheep blood (5%), is suitable for isolation and growth of fastidious microorganisms such as streptococci, staphylococci, pneumococci and listeriae from clinical samples.
UOM: 1 * 5 kg
Product Image-HOIT40042M-XL-BULK

Shoe covers, PP/CPE

Supplier: HUBEI ORIENT INTL TRADING
Description: These non woven shoe covers are made of PP with a skid-resistant CPE coating on the sole.

Image Unavailable-APOSBISN0153-10MG

IPI-549

Supplier: Apollo Scientific
Description: IPI-549 is a selective phosphoinositide-3-kinase (PI3K)-γ inhibitor with IC50 of 16 nM as an immuno-oncology clinical candidate.

Image Unavailable-BOSSBS-7974R-CY3

Anti-ATXN2 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-7974R-CY3)
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-BOSSBS-7974R-CY5.5

Anti-ATXN2 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-7974R-CY5.5)
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-BOSSBS-10044R-A680

Anti-Newcastle disease virus Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-10044R-A680)
Supplier: Bioss
Description: 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
Image Unavailable-BOSSBS-4807R-CY3

Anti-ATXN3L Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-4807R-CY3)
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-620-2424

VWR® Traceable®, Digital Thermometer, Platinum, Clinical Trials

Catalog Number: (620-2424)
Supplier: VWR Collection
Description: These platinum clinical trial thermometers are used to monitor the temperature in water baths, heating blocks and incubators. They display min/max temperatures for the previous 24 hours (each hour) and previous seven days (for each days); or previous 31 days (for each day).
UOM: 1 * 1 items
Product Image-GOJO9661-24EEU00

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.

Product Image-113-8320

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.

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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.
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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