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RESTEK
Artikel-Nr:
(APOSBIT1043-1MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
BIT1043-1MG
Lokale Artikelnummer::
APOSBIT1043-1MG
Beschreibung:
T2 Tetraol
VE:
1 * 1 mg
Lieferant:
HICHROM GAS CHROMATOGRAPHY
Beschreibung:
Allzweck-Phase für eine Vielzahl von Anwendungen mit geringer bis mittlerer Polarität, darunter (zum Beispiel): Lösungsmittelrückstände und flüchtige Schadstoffe.
Artikel-Nr:
(BOSSBS-9626R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9626R-A680
Lokale Artikelnummer::
BOSSBS-9626R-A680
Beschreibung:
RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9626R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9626R-A488
Lokale Artikelnummer::
BOSSBS-9626R-A488
Beschreibung:
RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
VE:
1 * 100 µl
Artikel-Nr:
(1.12264.0500)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.12264.0500
Lokale Artikelnummer::
MERC1.12264.0500
Beschreibung:
di-Natriumhydrogencitrat Sesquihydat, Sigma-Aldrich®
VE:
1 * 500 g
Lieferant:
KEYSTONE CLEANROOM PRODUCTS
Beschreibung:
Die Heavy-Duty-SMS-Verpackungsfolien von Keystone Cleanroom Products bieten eine hervorragende mikrobielle Barriere. Ideal für pharmazeutische Produktionsanwendungen.
Artikel-Nr:
(BOSSBS-3524R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3524R-CY5.5
Lokale Artikelnummer::
BOSSBS-3524R-CY5.5
Beschreibung:
PED/PEA 15 (Phosphoprotein Enriched in Diabetes/Phosphoprotein Enriched in Astrocytes 15 kDa) is a widely expressed 15 kDa protein comprised of an N terminal region containing a canonical Death Effector Domain (DED) sequence and a nuclear export signal, and a C terminal region containing two serine phosphorylation sites. PED/PEA 15 has been implicated in the regulation of multiple cellular processes including apoptosis, integrin activation, and insulin sensitive glucose transport in insulin responsive cells. Phosphorylation of both serine 104 (a Protein Kinase C site) and serine 116 (a substrate of CaMKII and Akt) is required for PED/PEA 15 function.
VE:
1 * 100 µl
Lieferant:
JULABO GmbH
Beschreibung:
Tubing made of stainless steel 1.4404 for use with all Presto process systems.
Lieferant:
Alfa Aesar
Beschreibung:
Galena is used in infrared detectors, photo optic applications, slip property modifier used in friction industry for enhancing heat conduction and regulating friction coefficient, used as a semiconductor. Used in electronic devices and Infrared sensor.
Artikel-Nr:
(BOSSBS-13326R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-A350
Lokale Artikelnummer::
BOSSBS-13326R-A350
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8654R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8654R-FITC
Lokale Artikelnummer::
BOSSBS-8654R-FITC
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(APOSBITH3057-25MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
BITH3057-25MG
Lokale Artikelnummer::
APOSBITH3057-25MG
Beschreibung:
Thymopentin
VE:
1 * 25 mg
Lieferant:
Thermo Scientific
Beschreibung:
CAS No.: 583-93-7
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,2-Dimethylglutarsäure
Lieferant:
HICHROM GAS CHROMATOGRAPHY
Beschreibung:
Nützlich für die Analyse chiraler Verbindungen in Duftstoffen, Pestiziden und Pharmazeutika, bei denen die Bestimmung des Enantiomerenverhältnisses in einer Probe erforderlich ist.
Artikel-Nr:
(BOSSBS-6505R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6505R-A488
Lokale Artikelnummer::
BOSSBS-6505R-A488
Beschreibung:
Lipoxygenases are a family of enzymes which dioxygenate unsaturated fatty acids, thus initiating lipoperoxidation of membranes and synthesis of signaling molecules, as well as inducing structural and metabolic changes in the cell. The Lox enzymes in mammals include 12-LO and 15-LO, which are classified with respect to their positional specificity of the deoxygenation of their most common substrate, arachidonic acid. The metabolism of arachidonic acid leads to the generation of biologically active metabolites that have been implicated in cell growth and proliferation, as well as survival and apoptosis. 15-Lipoxygenase (15-LO) acts in physiological membrane remodeling and the pathogenesis of atherosclerosis, inflammation, and carcinogenesis. It is highly regulated and expressed in a tissue- and cell-type-specific fashion. IL-4 and IL-13 play important roles in transactivating the 15-LO gene. Overexpression of 15-LO type 1 in prostate cancer contributes to the cancer progression by regulating IGF-1R expression and activation.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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