2-Fluorisonicotins\u00E4ure
Lieferant:
TENAK
Beschreibung:
Edelstahl.
Artikel-Nr:
(BOSSBS-6505R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6505R-A555
Lokale Artikelnummer::
BOSSBS-6505R-A555
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
Artikel-Nr:
(BOSSBS-6505R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6505R-HRP
Lokale Artikelnummer::
BOSSBS-6505R-HRP
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Brom-2-nitroanilin 98%
Artikel-Nr:
(MFLX06602-24)
Lieferant:
Avantor Fluid Handling
Hersteller-Artikelnummer::
06602-24
Lokale Artikelnummer::
MFLB06602-24
Beschreibung:
Strapazierfähiger als Standard-PVC.
VE:
1 * 100 Fuß
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Artikel-Nr:
(HONCR1022-10MG)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
R1022-10MG
Lokale Artikelnummer::
HONCR1022-10MG
Beschreibung:
Organic Standard, Cimaterol-d₇, Packung: Glass Bottle
VE:
1 * 10 mg
Lieferant:
Alfa Aesar
Beschreibung:
Kupfer(II)phthalocyanin
Artikel-Nr:
(BLDPBD249058-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD249058-100MG
Lokale Artikelnummer::
BLDPBD249058-100MG
Beschreibung:
3-Ethoxy-5-hydroxybenzaldehyde 96%
VE:
1 * 100 mg
Lieferant:
SCHURR SCHUHVERTRIEB
Beschreibung:
Antistatischen Chiro Clogs aus PU.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,5-Bis(trifluoromethyl)-2,6-dichlorobenzal chloride
Artikel-Nr:
(CAYM35670-100)
Lieferant:
Cayman Chemical
Hersteller-Artikelnummer::
35670-100
Lokale Artikelnummer::
CAYM35670-100
Beschreibung:
A ligand for copper(I)-catalysed azide/alkyne cycloaddition.
VE:
1 * 100 mg
Artikel-Nr:
(HECH40624010)
Lieferant:
GLASWARENFABRIK KARL HECHT
Hersteller-Artikelnummer::
40624010
Lokale Artikelnummer::
HECH40624010
Beschreibung:
Glass spot plates with 10 or 12 numbered cavities. For flocculation tests.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-8654R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8654R-A555
Lokale Artikelnummer::
BOSSBS-8654R-A555
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:
(BOSSBS-13326R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-FITC
Lokale Artikelnummer::
BOSSBS-13326R-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 LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11012R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11012R-A555
Lokale Artikelnummer::
BOSSBS-11012R-A555
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 FAM98 gene product has been provisionally designated FAM98 pending further characterization.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-(2-Fluorophenyl)-2-piperidone 95%
Preis auf Anfrage
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