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Codice catalogo: (BOSSBS-6009R)
Fornitore: Bioss
Codice articolo fornitore: BS-6009R
Codice articolo locale: BOSSBS-6009R
Descrizione: This gene includes 11 exons spanning 25 kb and maps to a region of chromosome 16 that is sometimes deleted in breast and prostrate cancer. The second intron contains an apparently intronless gene, C16orf3, that is transcribed in the opposite orientation. This gene is a putative tumor suppressor gene.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13692R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-13692R-A555
Codice articolo locale: BOSSBS-13692R-A555
Descrizione: MS4A6A is a member of the membrane-spanning 4A gene family and may be involved in signal transduction as a component of a multimeric receptor complex. There are three named isoforms.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-7514R)
Fornitore: Bioss
Codice articolo fornitore: BS-7514R
Codice articolo locale: BOSSBS-7514R
Descrizione: BAI1, a p53-target gene, encodes brain-specific angiogenesis inhibitor, a seven-span transmembrane protein and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities and may also play a role in angiogenesis.
UOM: 1 * 100 µl


Codice catalogo: (J575-1G)
Fornitore: VWR Chemicals
Codice articolo locale: VWRCJ575-1G
Descrizione: Detergente non ionico separa in modo efficiente le proteine ​​idrofile trans membrana, le proteine ​​idrofobiche senza alterarne l'attività biologica.
UOM: 1 * 1 g

MSDS


Codice catalogo: (BOSSBS-7514R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-7514R-CY7
Codice articolo locale: BOSSBS-7514R-CY7
Descrizione: BAI1, a p53-target gene, encodes brain-specific angiogenesis inhibitor, a seven-span transmembrane protein and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities and may also play a role in angiogenesis.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-8042R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-8042R-A750
Codice articolo locale: BOSSBS-8042R-A750
Descrizione: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 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. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-8042R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-8042R-HRP
Codice articolo locale: BOSSBS-8042R-HRP
Descrizione: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 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. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-3410R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-3410R-HRP
Codice articolo locale: BOSSBS-3410R-HRP
Descrizione: Signaling adapter that couples activated growth factor receptors to signaling pathways. Participates in a signaling cascade initiated by activated KIT and KITLG/SCF. Isoform p46Shc and isoform p52Shc, once phosphorylated, couple activated receptor tyrosine kinases to Ras via the recruitment of the GRB2/SOS complex and are implicated in the cytoplasmic propagation of mitogenic signals. Isoform p46Shc and isoform p52Shc may thus function as initiators of the Ras signaling cascade in various non-neuronal systems. Isoform p66Shc does not mediate Ras activation, but is involved in signal transduction pathways that regulate the cellular response to oxidative stress and life span. Isoform p66Shc acts as a downstream target of the tumor suppressor p53 and is indispensable for the ability of stress-activated p53 to induce elevation of intracellular oxidants, cytochrome c release and apoptosis. The expression of isoform p66Shc has been correlated with life span (By similarity). Participates in signaling downstream of the angiopoietin receptor TEK/TIE2, and plays a role in the regulation of endothelial cell migration and sprouting angiogenesis.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-3410R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-3410R-CY5.5
Codice articolo locale: BOSSBS-3410R-CY5.5
Descrizione: Signaling adapter that couples activated growth factor receptors to signaling pathways. Participates in a signaling cascade initiated by activated KIT and KITLG/SCF. Isoform p46Shc and isoform p52Shc, once phosphorylated, couple activated receptor tyrosine kinases to Ras via the recruitment of the GRB2/SOS complex and are implicated in the cytoplasmic propagation of mitogenic signals. Isoform p46Shc and isoform p52Shc may thus function as initiators of the Ras signaling cascade in various non-neuronal systems. Isoform p66Shc does not mediate Ras activation, but is involved in signal transduction pathways that regulate the cellular response to oxidative stress and life span. Isoform p66Shc acts as a downstream target of the tumor suppressor p53 and is indispensable for the ability of stress-activated p53 to induce elevation of intracellular oxidants, cytochrome c release and apoptosis. The expression of isoform p66Shc has been correlated with life span (By similarity). Participates in signaling downstream of the angiopoietin receptor TEK/TIE2, and plays a role in the regulation of endothelial cell migration and sprouting angiogenesis.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-8042R)
Fornitore: Bioss
Codice articolo fornitore: BS-8042R
Codice articolo locale: BOSSBS-8042R
Descrizione: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 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. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
UOM: 1 * 100 µl


Fornitore: PROVITRO
Descrizione: Natural Killer cells (NK cells) constitute a lymphocytic subset of the immune system and play a crucial role in immunological surveillance and host defence. Their significance spans across various areas such as bone marrow transplantation, cancer, pregnancy, autoimmune diseases, viral infections, and increasingly in adaptive immunity.

New Product

Fornitore: VWR Collection
Descrizione: In acciaio inox. Pinze robuste e di facile utilizzo.

Codice catalogo: (BOSSBS-7609R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-7609R-CY5
Codice articolo locale: BOSSBS-7609R-CY5
Descrizione: DUSP2 is a dual-specific thr/tyr phosphatase that is a physiologically relevant MAP kinase phosphatase. The gene is located on 2q11.2-q11 and contains 4 exons that span approximately 2.3kb. Under specific stress conditions, p53 regulates transcription of PAC1 through a new p53-binding site, and that PAC1 is necessary and sufficient for p53-mediated apoptosis.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-7514R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-7514R-A488
Codice articolo locale: BOSSBS-7514R-A488
Descrizione: BAI1, a p53-target gene, encodes brain-specific angiogenesis inhibitor, a seven-span transmembrane protein and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities and may also play a role in angiogenesis.
UOM: 1 * 100 µl


Codice catalogo: (M144-1L)
Fornitore: VWR Chemicals
Codice articolo locale: VWRCM144-1L
Descrizione: Detergente non ionico separa efficacemente proteine ​​idrofile trans membrana, proteine ​​idrofobiche senza alterarne l'attività biologica.
UOM: 1 * 1 L

Codice catalogo: (BOSSBS-10516R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-10516R-A680
Codice articolo locale: BOSSBS-10516R-A680
Descrizione: This gene encodes a high affinity receptor for the peptide hormone calcitonin and belongs to a subfamily of seven transmembrane-spanning G protein-coupled receptors. The encoded protein is involved in maintaining calcium homeostasis and in regulating osteoclast-mediated bone resorption. Polymorphisms in this gene have been associated with variations in bone mineral density and onset of osteoporosis. Alternate splicing results in multiple transcript variants.
UOM: 1 * 100 µl


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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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