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Image Unavailable-BOSSBS-3472R-FITC

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

Varenummer: (BOSSBS-3472R-FITC)
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-A555

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

Varenummer: (BOSSBS-9018R-A555)
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-A555

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

Varenummer: (BOSSBS-3472R-A555)
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-3472R-A488

Anti-VIM Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Varenummer: (BOSSBS-3472R-A488)
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-A350

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

Varenummer: (BOSSBS-9018R-A350)
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-15130R-CY7

Anti-C21orf88 Rabbit Polyclonal Antibody (Cy7®)

Varenummer: (BOSSBS-15130R-CY7)
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-15130R-A555

Anti-C21orf88 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Varenummer: (BOSSBS-15130R-A555)
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-15130R-A647

Anti-C21orf88 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Varenummer: (BOSSBS-15130R-A647)
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-FITC

Anti-ITGA5 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Varenummer: (BOSSBS-5791R-FITC)
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-9976R-A680

Anti-C21orf128 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Varenummer: (BOSSBS-9976R-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 C21orf128 gene product has been provisionally designated C21orf128 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9975R-A750

Anti-C21ORF62 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Varenummer: (BOSSBS-9975R-A750)
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 C21orf62 gene product has been provisionally designated C21orf62 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12568R

Anti-ACTL6A Rabbit Polyclonal Antibody

Varenummer: (BOSSBS-12568R)
Leverandør: Bioss
Beskrivelse: The SWI/SNF complex regulates gene expression via ATP-dependent chromatin remodeling. Brm (SNF2-a), Brg-1 (SNF2-b), Ini1 (integrase interactor 1, SNF5), BAF53 (ARPn beta), BAF57, BAF155 (SRG3), and BAF170 make up the functional core. BAF53 homologues from yeast to humans contain a conserved N-terminal motif, which contains residues at serine 2 and tyrosine 6, which play important roles in BAF53 activity. The BAF53 protein shuttles between the nucleus and cytoplasm. BAF53 also forms a complex with TIP49 and TIP48, which mediates c-Myc oncogenic activity.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6798R-A647

Anti-CAPN12 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Varenummer: (BOSSBS-6798R-A647)
Leverandør: Bioss
Beskrivelse: Calpains are a family of cytosolic calcium activated cysteine proteases involved in a variety of cellular processes including apoptosis, cell division, modulation of integrin and cytoskeletal interactions, and synaptic plasticity. Calpain 12 was first described in the mouse, most strongly in the skin, and maps to mouse chromosome 7. Isoforms differ in the carboxyterminal ends, ending with aberrant domain III and lacking domain IV. Domains in the large subunit include the amino terminal domain I, the proteinase domain II, domain III, and the EF hand domain IV, making Calpain 12 most similar to calpains 1 and 2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15258R-CY3

Anti-C7ORF13 Rabbit Polyclonal Antibody (Cy3)

Varenummer: (BOSSBS-15258R-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 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.
UOM: 1 * 100 µl
Image Unavailable-BDAM382258

Perifer IV-kanyle, BD Angiocath™

Leverandør: BD Medical
Beskrivelse: The BD Angiocath™ and BD Angiocath™ special IV catheters offer a wide range of products designed to provide peripheral vascular access to help meet clinicians' needs. The catheters are made with FEP material with a clear flash chamber to help make blood flashback easily identifiable.

Product Image-BRDY805842

Safety lockouts

Leverandør: Brady
Beskrivelse: These lockouts make sure all machinery stays locked until every individual working on the repairs or inspection is finished. Each person puts a lock on the hasp, but the hasp cannot be removed until all lockouts have been removed, thus preventing accidents.

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