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Image Unavailable-BOSSBS-15270R-A647

Anti-C7ORF45 Rabbit Polyclonal Antibody (ALEXA FLUOR® 647)

Código de Artigo: (BOSSBS-15270R-A647)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf45 gene product has been provisionally designated C7orf45 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15270R-A555

Anti-C7ORF45 Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

Código de Artigo: (BOSSBS-15270R-A555)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf45 gene product has been provisionally designated C7orf45 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15267R-A647

Anti-C7ORF43 Rabbit Polyclonal Antibody (ALEXA FLUOR® 647)

Código de Artigo: (BOSSBS-15267R-A647)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf43 gene product has been provisionally designated C7orf43 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15261R-A750

Anti-C7ORF26 Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

Código de Artigo: (BOSSBS-15261R-A750)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf26 gene product has been provisionally designated C7orf26 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15261R-A350

Anti-C7ORF26 Rabbit Polyclonal Antibody (ALEXA FLUOR® 350)

Código de Artigo: (BOSSBS-15261R-A350)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf26 gene product has been provisionally designated C7orf26 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15257R-A555

Anti-C7ORF10 Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

Código de Artigo: (BOSSBS-15257R-A555)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-ENZOADICSA509E

Anti-SARM Rabbit Polyclonal Antibody

Código de Artigo: (ENZOADICSA509E)
Fornecedor: ENZO LIFE SCIENCES
Descrição: SARM (SAM and ARM-containing protein) is thought to serve as an adaptor protein for the Toll-like receptors (TLRs) and allow for the activation of downstream kinases and NF-κB, ultimately leading to the expression of proteins involved in host defense.
UOM: 1 * 100 µG
Imagem do Produto-PIER22330

BMH (1,6-Bis(maleimido)hexane), Pierce™

Código de Artigo: (PIER22330)
Fornecedor: Thermo Fisher Scientific
Descrição: Thermo Scientific Pierce BMH is a long-arm, maleimide crosslinker for covalent, irreversible conjugation between sulfhydryl groups (e.g., protein or peptide cysteines).
UOM: 1 * 50 mg
Image Unavailable-BOSSBS-15267R-CY3

Anti-C7ORF43 Rabbit Polyclonal Antibody (Cy3)

Código de Artigo: (BOSSBS-15267R-CY3)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf43 gene product has been provisionally designated C7orf43 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15270R-CY3

Anti-C7ORF45 Rabbit Polyclonal Antibody (Cy3)

Código de Artigo: (BOSSBS-15270R-CY3)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf45 gene product has been provisionally designated C7orf45 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15257R-FITC

Anti-C7ORF10 Rabbit Polyclonal Antibody (FITC)

Código de Artigo: (BOSSBS-15257R-FITC)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15261R-HRP

Anti-C7ORF26 Rabbit Polyclonal Antibody (HRP)

Código de Artigo: (BOSSBS-15261R-HRP)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf26 gene product has been provisionally designated C7orf26 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15271R-CY7

Anti-C7ORF46 Rabbit Polyclonal Antibody (Cy7)

Código de Artigo: (BOSSBS-15271R-CY7)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf46 gene product has been provisionally designated C7orf46 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15257R-CY7

Anti-C7ORF10 Rabbit Polyclonal Antibody (Cy7)

Código de Artigo: (BOSSBS-15257R-CY7)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15266R-CY5

Anti-C7ORF42 Rabbit Polyclonal Antibody (Cy5)

Código de Artigo: (BOSSBS-15266R-CY5)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf42 gene product has been provisionally designated C7orf42 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15266R-FITC

Anti-C7ORF42 Rabbit Polyclonal Antibody (FITC)

Código de Artigo: (BOSSBS-15266R-FITC)
Fornecedor: Bioss
Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf42 gene product has been provisionally designated C7orf42 pending further characterisation.
UOM: 1 * 100 µl
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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