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Imagem do Produto-521-3442

H-FLEX HS4 windshield swinging bucket rotor and accessories

Fornecedor: Thermo Scientific
Descrição: 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.

Imagem do Produto-LIOF96147

Latex tests

Código de Artigo: (LIOF96147)
Fornecedor: LIOFILCHEM
Descrição: Identification of the main pathogenic microorganisms directly from clinical specimens.
UOM: 1 * 1 unid.
Imagem do Produto-LIOF26490

VTM - virus transport medium

Código de Artigo: (LIOF26490)
Fornecedor: LIOFILCHEM
Descrição: 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 unid.

Certificados


Imagem do Produto-ENZOBMLNA1390001

Bupivacaine hydrochloride monohydrate ≥98% (por UHPLC), sólido branco

Código de Artigo: (ENZOBMLNA1390001)
Fornecedor: ENZO LIFE SCIENCES
Descrição: Sodium channel blocker. Clinically useful local anesthetic.
UOM: 1 * 1 g

Novo produto


Image Unavailable-BOSSBS-4807R-A750

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

Código de Artigo: (BOSSBS-4807R-A750)
Fornecedor: Bioss
Descrição: 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))

Código de Artigo: (BOSSBS-4807R-HRP)
Fornecedor: Bioss
Descrição: 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
Imagem do Produto-114-9035

Shoe covers, PP/CPE

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

Image Unavailable-ICNA091003122

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

Código de Artigo: (ICNA091003122)
Fornecedor: MP Biomedicals
Descrição: 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
Image Unavailable-BOSSBS-4807R-A350

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

Código de Artigo: (BOSSBS-4807R-A350)
Fornecedor: Bioss
Descrição: 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)

Código de Artigo: (BOSSBS-4807R-A555)
Fornecedor: Bioss
Descrição: 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®)

Código de Artigo: (BOSSBS-4807R-CY5.5)
Fornecedor: Bioss
Descrição: 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®)

Código de Artigo: (BOSSBS-4807R-CY5)
Fornecedor: Bioss
Descrição: 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
Imagem do Produto-630-3168

Upright microscopes, DM 1000 LED

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

Imagem do Produto-113-9049

VWR®, Isolation Gowns

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

Image Unavailable-OXOIS611430-6

Ag-AK, Immunofluorescence test, IMAGEN™

Fornecedor: THERMO FISHER DIAGNOSTICS
Descrição: IMAGEN™ is a qualitative direct immunofluorescence test used for detection and confirmation of the presence of virus in cell culture or in clinical specimen.

Imagem do Produto-113-9410

VWR®, Cleanroom Socks, ESD, Disposable

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

Environmentally Preferable Promoção

Preço sob consulta
O stock para este item é limitado. Por favor, certifique-se de que efetuou o seu login para visualizar o stock disponível. Se a call ainda é exibida e precisar de ajuda, por favor, ligue para 213 600 770
O stock para este item é limitado. Por favor, certifique-se de que efetuou o seu login para visualizar o stock disponível. Se a call está visível e precisar de ajuda, por favor, ligue para 213 600 770
Este produto é sujeito a regulamentação especifica.
Em caso de encomenda, será contactado a solicitar documentação complementar necessária e/ou obrigatória (licença, autorização ou declaração de uso final) para a continuidade do pedido. Agradecemos a vossa compreensão
Este produto é sujeito a regulamentação especifica.
Em caso de encomenda, será contactado a solicitar documentação complementar necessária e/ou obrigatória (licença, autorização ou declaração de uso final) para a continuidade do pedido. Agradecemos a vossa compreensão.
Este produto está bloqueado. Para obter mais informações, contacte a VWR através do número 213 600 770.
O produto pretendido já não se encontra disponível. O produto indicado é um substituto.
Este produto encontra-se em rutura de stock. Poderá encontrar alternativas pesquisando pelo código de artigo indicado acima. Se precisar de ajuda, por favor contacte a VWR através do 213 600 770.
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