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Procurou por: Arm\u00E1rios\/Arm\u00E1rios+Seguran\u00E7a


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Código de Artigo: (APOSBICL208-100MG)
Fornecedor: Apollo Scientific
Descrição: Spacer arm SPDPantibody-toxin conjugation
UOM: 1 * 100 mg


Código de Artigo: (ABCAAB214259-100)
Fornecedor: Abcam
Descrição: Anti-ADRM1/ARM-1 Rabbit Monoclonal Antibody [clone: EPR11449(B)] (Alexa Fluor® 647)
UOM: 1 * 100 µl


Código de Artigo: (ABCAAB211702-100)
Fornecedor: Abcam
Descrição: Anti-ADRM1/ARM-1 Rabbit Monoclonal Antibody [clone: EPR11449(B)] (PE)
UOM: 1 * 100 µl


Fornecedor: MIELE
Descrição: Accessories for Glassware washing machines, A 603 Attachment for the expansion of the A 500 mobile unit to 2 levels. With spray arm, W×D×H: 640×790×565 mm

Fornecedor: Brady
Descrição: These universal lockout devices are a modular system which enables users to lock out valves of different types and sises.

Fornecedor: Corning
Descrição: Vidro borossilicato com braços laterais, não estéril.
Código de Artigo: (APOSBICL200-100MG)
Fornecedor: Apollo Scientific
Descrição: Primary amine and Sulphhydryl reactive.Enzyme antibody conjugation - Spacer arm.
UOM: 1 * 100 mg


Código de Artigo: (ENZOBMLSE1020001)
Fornecedor: ENZO LIFE SCIENCES
Descrição: Isolated from bovine brain. Calmodulin conjugated to 4% cross-linked agarose beads via a 5 atom hydrophilic spacer arm.
UOM: 1 * 1 mL


Código de Artigo: (BOSSBS-5990R)
Fornecedor: Bioss
Descrição: This gene encodes a member of the ALEX family of proteins which may play a role in tumor suppression. The encoded protein contains a potential N-terminal transmembrane domain and a single Armadillo (arm) repeat. Other proteins containing the arm repeat are involved in development, maintenance of tissue integrity, and tumorigenesis. This gene is closely localized with other family members on the X chromosome. Three transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5990R-CY5.5)
Fornecedor: Bioss
Descrição: This gene encodes a member of the ALEX family of proteins which may play a role in tumor suppression. The encoded protein contains a potential N-terminal transmembrane domain and a single Armadillo (arm) repeat. Other proteins containing the arm repeat are involved in development, maintenance of tissue integrity, and tumorigenesis. This gene is closely localized with other family members on the X chromosome. Three transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5990R-CY3)
Fornecedor: Bioss
Descrição: This gene encodes a member of the ALEX family of proteins which may play a role in tumor suppression. The encoded protein contains a potential N-terminal transmembrane domain and a single Armadillo (arm) repeat. Other proteins containing the arm repeat are involved in development, maintenance of tissue integrity, and tumorigenesis. This gene is closely localized with other family members on the X chromosome. Three transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-15262R-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 C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-15262R-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 C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-15266R-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 C7orf42 gene product has been provisionally designated C7orf42 pending further characterisation.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-15269R-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 C7orf44 gene product has been provisionally designated C7orf44 pending further characterisation.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-15273R-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 C7orf53 gene product has been provisionally designated C7orf53 pending further characterisation.
UOM: 1 * 100 µl


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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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