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Image Unavailable-BOSSBS-15270R

Anti-C7orf45 Rabbit Polyclonal Antibody

Código de Artigo: (BOSSBS-15270R)
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 characterized 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 characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5990R-FITC

Anti-ARMCX3 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Código de Artigo: (BOSSBS-5990R-FITC)
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
Image Unavailable-BOSSBS-5990R-HRP

Anti-ARMCX3 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Código de Artigo: (BOSSBS-5990R-HRP)
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
Image Unavailable-BOSSBS-15279R-CY5

Anti-C7ORF64 Rabbit Polyclonal Antibody (Cy5)

Código de Artigo: (BOSSBS-15279R-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 C7orf64 gene product has been provisionally designated C7orf64 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15271R-CY5

Anti-C7ORF46 Rabbit Polyclonal Antibody (Cy5)

Código de Artigo: (BOSSBS-15271R-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 C7orf46 gene product has been provisionally designated C7orf46 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15271R-FITC

Anti-C7ORF46 Rabbit Polyclonal Antibody (FITC)

Código de Artigo: (BOSSBS-15271R-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 C7orf46 gene product has been provisionally designated C7orf46 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15266R-CY7

Anti-C7ORF42 Rabbit Polyclonal Antibody (Cy7)

Código de Artigo: (BOSSBS-15266R-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 C7orf42 gene product has been provisionally designated C7orf42 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15269R-HRP

Anti-C7ORF44 Rabbit Polyclonal Antibody (HRP)

Código de Artigo: (BOSSBS-15269R-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 C7orf44 gene product has been provisionally designated C7orf44 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15267R-FITC

Anti-C7ORF43 Rabbit Polyclonal Antibody (FITC)

Código de Artigo: (BOSSBS-15267R-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 C7orf43 gene product has been provisionally designated C7orf43 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-ABCAAB211702-100

Anti-ADRM1/ARM-1 Rabbit Monoclonal Antibody [clone: EPR11449(B)] (PE)

Código de Artigo: (ABCAAB211702-100)
Fornecedor: Abcam
Descrição: Anti-ADRM1/ARM-1 Rabbit Monoclonal Antibody [clone: EPR11449(B)] (PE)
UOM: 1 * 100 µl
Image Unavailable-ENZOBMLSE1020001

Bovine native Calmodulin (from Brain), Agarose

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
Imagem do Produto-139-0027

Particle counter transport cart

Código de Artigo: (139-0027)
Fornecedor: Palbam
Descrição: This cart is specially designed for transporting particle sensing machines around the cleanroom environment. Stainless steel 304 with electropolished finish.
UOM: 1 * 1 unid.
Imagem do Produto-BOSSBS-5988R

Anti-ARMCX1 Rabbit Polyclonal Antibody

Código de Artigo: (BOSSBS-5988R)
Fornecedor: Bioss
Descrição: This gene encodes a member of the ALEX family of proteins and may play a role in tumor suppression. The encoded protein contains a potential N-terminal transmembrane domain and two Armadillo (arm) repeats. 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, including ALEX2 and ALEX3, on the X chromosome. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15264R-A488

Anti-C7ORF34 Rabbit Polyclonal Antibody (ALEXA FLUOR® 488)

Código de Artigo: (BOSSBS-15264R-A488)
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 C7orf34 gene product has been provisionally designated C7orf34 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15274R-A750

Anti-C7ORF57 Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

Código de Artigo: (BOSSBS-15274R-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 C7orf57 gene product has been provisionally designated C7orf57 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15266R-A680

Anti-C7ORF42 Rabbit Polyclonal Antibody (ALEXA FLUOR® 680)

Código de Artigo: (BOSSBS-15266R-A680)
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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