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Image Unavailable-BOSSBS-15273R-A750

Anti-C7ORF53 Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

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.
Código de Artigo: BOSSBS-15273R-A750
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15274R-A488

Anti-C7ORF57 Rabbit Polyclonal Antibody (ALEXA FLUOR® 488)

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.
Código de Artigo: BOSSBS-15274R-A488
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15267R-A680

Anti-C7ORF43 Rabbit Polyclonal Antibody (ALEXA FLUOR® 680)

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.
Código de Artigo: BOSSBS-15267R-A680
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15269R-A750

Anti-C7ORF44 Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

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.
Código de Artigo: BOSSBS-15269R-A750
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15271R-A555

Anti-C7ORF46 Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

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.
Código de Artigo: BOSSBS-15271R-A555
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15270R-A750

Anti-C7ORF45 Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

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.
Código de Artigo: BOSSBS-15270R-A750
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-10471R-CY5

Anti-DYNC1I2 Rabbit Polyclonal Antibody (Cy5®)

Descrição: The inner- and outer-arm dyneins, which bridge between the doublet microtubules in axonemes, are the force-generating proteins responsible for the sliding movement in axonemes. The intermediate and light chains, thought to form the base of the dynein arm, help mediate attachment and may also participate in regulating dynein activity. This gene encodes an intermediate chain dynein, belonging to the large family of motor proteins. Mutations in this gene result in abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia (PCD) and Kartagener syndrome. [provided by RefSeq, Jul 2008].
Código de Artigo: BOSSBS-10471R-CY5
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-11024R-FITC

Anti-DNAI1/2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Descrição: The inner- and outer-arm dyneins, which bridge between the doublet microtubules in axonemes, are the force-generating proteins responsible for the sliding movement in axonemes. The intermediate and light chains, thought to form the base of the dynein arm, help mediate attachment and may also participate in regulating dynein activity. This gene encodes an intermediate chain dynein, belonging to the large family of motor proteins. Mutations in this gene result in abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia (PCD) and Kartagener syndrome. [provided by RefSeq, Jul 2008].
Código de Artigo: BOSSBS-11024R-FITC
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-11024R-A647

Anti-DNAI1/2 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descrição: The inner- and outer-arm dyneins, which bridge between the doublet microtubules in axonemes, are the force-generating proteins responsible for the sliding movement in axonemes. The intermediate and light chains, thought to form the base of the dynein arm, help mediate attachment and may also participate in regulating dynein activity. This gene encodes an intermediate chain dynein, belonging to the large family of motor proteins. Mutations in this gene result in abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia (PCD) and Kartagener syndrome. [provided by RefSeq, Jul 2008].
Código de Artigo: BOSSBS-11024R-A647
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-9018R-CY3

Anti-IQCE Rabbit Polyclonal Antibody (Cy3®)

Descrição: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. 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.
Código de Artigo: BOSSBS-9018R-CY3
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-9018R-A647

Anti-IQCE Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descrição: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. 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.
Código de Artigo: BOSSBS-9018R-A647
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-9018R-A680

Anti-IQCE Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Descrição: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. 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.
Código de Artigo: BOSSBS-9018R-A680
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-9018R

Anti-IQCE Rabbit Polyclonal Antibody

Descrição: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. 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.
Código de Artigo: BOSSBS-9018R
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-0096R-A555

Anti-SERPINA1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Descrição: Alpha-1-antitrypsin is a protease inhibitor, deficiency of which is associated with emphysema and liver disease. The protein is encoded by a gene (PI) located on the distal long arm of chromosome 14.
Código de Artigo: BOSSBS-0096R-A555
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15258R-A488

Anti-C7ORF13 Rabbit Polyclonal Antibody (ALEXA FLUOR® 488)

Descrição: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. 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 C7orf13 gene product has been provisionally designated C7orf13 pending further characterisation.
Código de Artigo: BOSSBS-15258R-A488
UOM: 1 * 100 µl
Fornecedor: Bioss
Imagem do Produto-112-2937

Sleeve protectors, cut resistant, VersaTouch® 72-290

Descrição: These sleeves are manufactured from a combination of PP, glass fibres and Dyneema®.
Código de Artigo: 112-2937
UOM: 1 * 1 unid.
Fornecedor: Ansell
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