Hai cercato: Tyrphostin+AG+835

Codice catalogo: (BOSSBS-7787R)

Fornitore: Bioss

Codice articolo fornitore: BS-7787R

Codice articolo locale: BOSSBS-7787R

Descrizione: Defects in CEP152 are the cause of microcephaly primary type 4 (MCPH4). A disease defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Affected individuals are mentally retarded. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits due to degenerative brain disorder.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BIRBORB98835-100)

Fornitore: Biorbyt

Codice articolo fornitore: ORB98835-100

Codice articolo locale: BIRBORB98835-100

Descrizione: CEA Ag

UOM: 1 * 100 µG

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Codice catalogo: (SCOC400580)

Fornitore: SCHOTT AG Lighting and imaging

Codice articolo fornitore: 400580

Codice articolo locale: SCOC400580

Descrizione: The diffusor for LED ring lights avoids reflections of LEDs for uniform illumination.

UOM: 1 * 1 pezzi

Promo

Codice catalogo: (BIRBORB98821-100)

Fornitore: Biorbyt

Codice articolo fornitore: ORB98821-100

Codice articolo locale: BIRBORB98821-100

Descrizione: Recombinant NSE Ag

UOM: 1 * 100 µG

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Codice catalogo: (BIRBORB98845-100)

Fornitore: Biorbyt

Codice articolo fornitore: ORB98845-100

Codice articolo locale: BIRBORB98845-100

Descrizione: Recombinant SCCA2 Ag

UOM: 1 * 100 µG

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Codice catalogo: (BIRBORB98850-100)

Fornitore: Biorbyt

Codice articolo fornitore: ORB98850-100

Codice articolo locale: BIRBORB98850-100

Descrizione: Recombinant CK8 Ag

UOM: 1 * 100 µG

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Codice catalogo: (456032M)

Fornitore: VWR Chemicals

Codice articolo locale: VWRC456032M

Descrizione: AgNO₃ in HNO₃ 2-5%

UOM: 1 * 100 mL

MSDS Certificati Promo

Codice catalogo: (BOSSBS-6325R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-6325R-FITC

Codice articolo locale: BOSSBS-6325R-FITC

Descrizione: Defects in SLC2A10 are the cause of arterial tortuosity syndrome (ATS) [MIM:208050]. ATS is an autosomal recessive disorder characterized by tortuosity and elongation of major arteries, often resulting in death at young age. Other typical features include aneurysms of large arteries and stenosis of the pulmonary artery, in association with facial features and several connective tissue manifestations such as soft skin and joint laxity. Histopathological findings include fragmentation of elastic fibers in the tunica media of large arteries.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15078R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15078R-CY3

Codice articolo locale: BOSSBS-15078R-CY3

Descrizione: C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15080R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15080R-CY3

Codice articolo locale: BOSSBS-15080R-CY3

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf87 gene product has been provisionally designated C1orf87 pending further characterization. There are three isoforms of C1orf87 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15040R-A555)

Fornitore: Bioss

Codice articolo fornitore: BS-15040R-A555

Codice articolo locale: BOSSBS-15040R-A555

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf177 gene product has been provisionally designated C1orf177 pending further characterization. There are two isoforms of C1orf177 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15034R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-15034R-CY5

Codice articolo locale: BOSSBS-15034R-CY5

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf167 gene product has been provisionally designated C1orf167 pending further characterization. There are two isoforms of C1orf167 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15035R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-15035R-CY7

Codice articolo locale: BOSSBS-15035R-CY7

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf168 gene product has been provisionally designated C1orf168 pending further characterization. There are two isoforms of C1orf168 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15035R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-15035R-A680

Codice articolo locale: BOSSBS-15035R-A680

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf168 gene product has been provisionally designated C1orf168 pending further characterization. There are two isoforms of C1orf168 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15035R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-15035R-A350

Codice articolo locale: BOSSBS-15035R-A350

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf168 gene product has been provisionally designated C1orf168 pending further characterization. There are two isoforms of C1orf168 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-7525R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-7525R-CY5

Codice articolo locale: BOSSBS-7525R-CY5

Descrizione: This gene encodes a protein that is related to chondromodulin-I, which is a cartilage-specific glycoprotein that functions to stimulate chondrocyte growth and to inhibit tube formation of endothelial cells. This protein is also an angiogenesis inhibitor. Genetic variation in this gene is associated with a risk for type 2 diabetes, central obesity and serum levels of systemic immune mediators in a body size-dependent manner. This gene is also a candidate gene for age-related macular degeneration, though a direct link has yet to be demonstrated. [provided by RefSeq, Sep 2009].

UOM: 1 * 100 µl

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