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Image Unavailable-BNC040294-100

Anti-NKX2-2 Mouse Monoclonal Antibody (CF405S) [clone: NX2/294]

Leverandør: Biotium
Beskrivelse: Expression of NKX2.2 has been found in neuroendocrine tumors of the gut, making it a potential marker for the study of gastrointestinal neuroendocrine tumors. More recently, NKX2.2 protein was identified as a target of EWS-FLI-1, the fusion protein specific to Ewing sarcoma, and was shown to be differentially upregulated in Ewing sarcoma on the basis of array-based gene expression analysis. It acts as a valuable marker for Ewing sarcoma, with a sensitivity of 93% and a specificity of 89%, and aids in the differential diagnosis of small round cell tumors.

Product Image-BARNSHKE416HP-1CE

Orbital shaker, benchtop, MaxQ™ HP

Varenummer: (BARNSHKE416HP-1CE)
Leverandør: Thermo Fisher Scientific
Beskrivelse: MaxQ™ HP benchtop orbital shaker suitable for environmental rooms or on lab benches. It features balancing technology and rugged mechanism make smooth high-capacity 24/7 shaking a reality, an industry-leading platform size, wide-range speed, low heat output motor and spill-resistant design. It features set point security which restricts unauthorised or inadvertent changes to key functions. Equipped with alarm to know the shaker performance.
UOM: 1 * 1 Items
Image Unavailable-BOSSBS-9018R-A680

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

Varenummer: (BOSSBS-9018R-A680)
Leverandør: Bioss
Beskrivelse: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9018R-CY3

Anti-IQCE Rabbit Polyclonal Antibody (Cy3®)

Varenummer: (BOSSBS-9018R-CY3)
Leverandør: Bioss
Beskrivelse: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9018R-A647

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

Varenummer: (BOSSBS-9018R-A647)
Leverandør: Bioss
Beskrivelse: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-3472R-A350

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

Varenummer: (BOSSBS-3472R-A350)
Leverandør: Bioss
Beskrivelse: This gene encodes a member of the intermediate filament family. Intermediate filamentents, along with microtubules and actin microfilaments, make up the cytoskeleton. The protein encoded by this gene is responsible for maintaining cell shape, integrity of the cytoplasm, and stabilizing cytoskeletal interactions. It is also involved in the immune response, and controls the transport of low-density lipoprotein (LDL)-derived cholesterol from a lysosome to the site of esterification. It functions as an organizer of a number of critical proteins involved in attachment, migration, and cell signaling. Mutations in this gene causes a dominant, pulverulent cataract.[provided by RefSeq, Jun 2009].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9018R

Anti-IQCE Rabbit Polyclonal Antibody

Varenummer: (BOSSBS-9018R)
Leverandør: Bioss
Beskrivelse: 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9974R-A680

Anti-C21ORF56 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Varenummer: (BOSSBS-9974R-A680)
Leverandør: Bioss
Beskrivelse: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf56 gene product has been provisionally designated C21orf56 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15130R-A680

Anti-C21orf88 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Varenummer: (BOSSBS-15130R-A680)
Leverandør: Bioss
Beskrivelse: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5791R-A555

Anti-ITGA5 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Varenummer: (BOSSBS-5791R-A555)
Leverandør: Bioss
Beskrivelse: Integrins are heterodimeric cell surface receptors composed of alpha and beta subunits, which mediate cell-cell and cell-extracellular matrix attachments. Aberrant integrin expression has been found in many epithelial tumours. Changes in integrin expression have been shown to be important for the growth and early metastatic capacity of melanoma cells. Integrin alpha-v beta-6 is upregulated in cancers and during tissue remodelling but is absent from resting adult tissues. Integrin alpha-v beta-6 promotes invasion and correlates with poor survival and therefore makes a promising therapeutic target.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5791R-CY7

Anti-ITGA5 Rabbit Polyclonal Antibody (Cy7®)

Varenummer: (BOSSBS-5791R-CY7)
Leverandør: Bioss
Beskrivelse: Integrins are heterodimeric cell surface receptors composed of alpha and beta subunits, which mediate cell-cell and cell-extracellular matrix attachments. Aberrant integrin expression has been found in many epithelial tumours. Changes in integrin expression have been shown to be important for the growth and early metastatic capacity of melanoma cells. Integrin alpha-v beta-6 is upregulated in cancers and during tissue remodelling but is absent from resting adult tissues. Integrin alpha-v beta-6 promotes invasion and correlates with poor survival and therefore makes a promising therapeutic target.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5791R-CY5.5

Anti-ITGA5 Rabbit Polyclonal Antibody (Cy5.5®)

Varenummer: (BOSSBS-5791R-CY5.5)
Leverandør: Bioss
Beskrivelse: Integrins are heterodimeric cell surface receptors composed of alpha and beta subunits, which mediate cell-cell and cell-extracellular matrix attachments. Aberrant integrin expression has been found in many epithelial tumours. Changes in integrin expression have been shown to be important for the growth and early metastatic capacity of melanoma cells. Integrin alpha-v beta-6 is upregulated in cancers and during tissue remodelling but is absent from resting adult tissues. Integrin alpha-v beta-6 promotes invasion and correlates with poor survival and therefore makes a promising therapeutic target.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9982R-A680

Anti-C21orf87 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Varenummer: (BOSSBS-9982R-A680)
Leverandør: Bioss
Beskrivelse: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf87 gene product has been provisionally designated C21orf87 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15130R-A350

Anti-C21orf88 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Varenummer: (BOSSBS-15130R-A350)
Leverandør: Bioss
Beskrivelse: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5791R-HRP

Anti-ITGA5 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Varenummer: (BOSSBS-5791R-HRP)
Leverandør: Bioss
Beskrivelse: Integrins are heterodimeric cell surface receptors composed of alpha and beta subunits, which mediate cell-cell and cell-extracellular matrix attachments. Aberrant integrin expression has been found in many epithelial tumours. Changes in integrin expression have been shown to be important for the growth and early metastatic capacity of melanoma cells. Integrin alpha-v beta-6 is upregulated in cancers and during tissue remodelling but is absent from resting adult tissues. Integrin alpha-v beta-6 promotes invasion and correlates with poor survival and therefore makes a promising therapeutic target.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9978R-A680

Anti-C21orf58 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Varenummer: (BOSSBS-9978R-A680)
Leverandør: Bioss
Beskrivelse: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf58 gene product has been provisionally designated C21orf58 pending further characterisation.
UOM: 1 * 100 µl
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