Print…

You Searched For: Clinical+Analysers


69 544  results were found

Refine Results Sort by
SearchResultCount:"69544"

Sort Results

List View Easy View

Rate These Search Results

Product Image-054353.

SGE GC Capillary Column, BP225

Catalog Number: (054353.)
Supplier: Trajan Scientific and Medical
Description: <p><span style="color:black">The SGE BP225 Capillary Column provides a great mid-polarity option for GC analyses. Recommended for FAMEs, carbohydrates, neutral sterols, flavor compounds, and sugars.</span></p>
UOM: 1 * 1 items
Image Unavailable-ICNA0210031925

β-Nicotinamide adenine dinucleotid, oxidised form (NAD, oxidised form) ≥93%

Supplier: MP Biomedicals
Description: This grade of NAD is intended for applications where maximum reagent purity is not critical. Well suited for use on most automatic analysers.

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
Image Unavailable-A7847-100MG

Acridine Orange 10-nonyl bromide (NAO), Sigma-Aldrich®

Catalog Number: (A7847-100MG)
Supplier: SIGMA ALDRICH MICROSCOPY
Description: Metachromatic dye useful as a mitochondrial probe in living cells. This dye has been used to analyse mitochondria by flow cytometry, characterise multidrug resistance, and measure changes in mitochondrial mass during apoptosis in rat thymocytes.
UOM: 1 * 100 mg
Product Image-AATB17543

Nuclear Violet™ LCS1

Catalog Number: (AATB17543)
Supplier: AAT BIOQUEST
Description: Our Nuclear Violet™ LCS1 is a fluorogenic, DNA-selective and cell-permeant dye for analysing DNA content in living cells.
UOM: 1 * 0,5 mL
Product Image-554-2917

Reversed phase chromatography columns, RSpak DC-613

Supplier: Resonac
Description: These columns are used to separate by combination of ligand exchange and HILIC modes and can analyse sugars without removing sodium salts in the sample.

Image Unavailable-PROOVHG-VPTPMO-25G

Elemental analysis standards, PTP sample of oils, VHG

Catalog Number: (PROOVHG-VPTPMO-25G)
Supplier: LGC Standards PROMOCHEM
Description: The PTP has been specially designed for analytical laboratories that analyse new and used oils for metals, sulphur, viscosity and particle count.
UOM: 1 * 25 g
Product Image-521-3441

H-FLEX HS4 windshield swinging bucket rotor and accessories

Supplier: Thermo Scientific
Description: 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.

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-AATB17552

Nuclear Red™ DCS1

Catalog Number: (AATB17552)
Supplier: AAT BIOQUEST
Description: Our Nuclear Red™ DCS1 is a fluorogenic, DNA-selective and cell-impermeant dye for analysing DNA content in dead, fixed or apoptotic cells.
UOM: 1 * 0,5 mL
Product Image-DIDAPOD068570_UK

Laurent polarimeters

Catalog Number: (DIDAPOD068570_UK)
Supplier: DIDALAB
Description: The Laurent polarimeter is composed of one lens fitted on graduated rule, and one housing for observation tubes, within which the substances to be analysed are introduced.
UOM: 1 * 1 items
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
Inquire for Price
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.
897 - 912 of 69 544
no targeter for Bottom