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1,2-Dibromethan
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1,2-Dibromethan
Artikel-Nr:
(APOSOR80497-25G)
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
10-Methoxy-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-4-one 25g pack 1 * 25 g
VE:
New Product
Artikel-Nr:
(BOSSBS-11822R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-CY3
Lokale Artikelnummer::
BOSSBS-11822R-CY3
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR33384-500MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR33384-500MG
Lokale Artikelnummer::
APOSOR33384-500MG
Beschreibung:
3-Benzyl-4-hydroxy-1-(prop-2-yn-1-yl)-1,2-dihydropyridin-2-one 500mg pack 1 * 500 mg
VE:
1 * 500 mg
New Product
Artikel-Nr:
(APOSOR33383-500MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR33383-500MG
Lokale Artikelnummer::
APOSOR33383-500MG
Beschreibung:
3-Benzyl-1-[(furan-2-yl)methyl]-4-hydroxy-1,2-dihydropyridin-2-one 500mg pack 1 * 500 mg
VE:
1 * 500 mg
New Product
Artikel-Nr:
(BOSSBS-6143R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6143R-A488
Lokale Artikelnummer::
BOSSBS-6143R-A488
Beschreibung:
May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2655R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2655R-CY3
Lokale Artikelnummer::
BOSSBS-2655R-CY3
Beschreibung:
Low-affinity receptor for leukotrienes including leukotriene B4. Mediates chemotaxis of granulocytes and macrophages. The response is mediated via G-proteins that activate a phosphatidylinositol-calcium second messenger system. The rank order of affinities for the leukotrienes is LTB4 >12-epi-LTB4 >LTB5 >LTB3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7796R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7796R-CY3
Lokale Artikelnummer::
BOSSBS-7796R-CY3
Beschreibung:
This gene encodes a kinetochore protein that functions aspart of the minichromosome instability-12 centromere complex. Theencoded protein is required for proper kinetochore assembly andprogression through the cell cycle. Alternative splicing results inmultiple transcript variants. [provided by RefSeq, Feb 2009].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2655R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2655R-CY7
Lokale Artikelnummer::
BOSSBS-2655R-CY7
Beschreibung:
Low-affinity receptor for leukotrienes including leukotriene B4. Mediates chemotaxis of granulocytes and macrophages. The response is mediated via G-proteins that activate a phosphatidylinositol-calcium second messenger system. The rank order of affinities for the leukotrienes is LTB4 >12-epi-LTB4 >LTB5 >LTB3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-CY7
Lokale Artikelnummer::
BOSSBS-11945R-CY7
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-CY5
Lokale Artikelnummer::
BOSSBS-11945R-CY5
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-CY5.5
Lokale Artikelnummer::
BOSSBS-8229R-CY5.5
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11003R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-CY7
Lokale Artikelnummer::
BOSSBS-11003R-CY7
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10368R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10368R-A680
Lokale Artikelnummer::
BOSSBS-10368R-A680
Beschreibung:
Receptor for lysophosphatidic acid (LPA), a mediator of diverse cellular activities. Seems to be coupled to the G(i)/G(o), G(12)/G(13), and G(q) families of heteromeric G proteins. Plays a key role in phospholipase C-beta (PLC-beta) Signalling pathway. Stimulates phospholipase C (PLC) activity in a manner that is independent of RALA activation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10368R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10368R-A750
Lokale Artikelnummer::
BOSSBS-10368R-A750
Beschreibung:
Receptor for lysophosphatidic acid (LPA), a mediator of diverse cellular activities. Seems to be coupled to the G(i)/G(o), G(12)/G(13), and G(q) families of heteromeric G proteins. Plays a key role in phospholipase C-beta (PLC-beta) Signalling pathway. Stimulates phospholipase C (PLC) activity in a manner that is independent of RALA activation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2655R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2655R-FITC
Lokale Artikelnummer::
BOSSBS-2655R-FITC
Beschreibung:
Low-affinity receptor for leukotrienes including leukotriene B4. Mediates chemotaxis of granulocytes and macrophages. The response is mediated via G-proteins that activate a phosphatidylinositol-calcium second messenger system. The rank order of affinities for the leukotrienes is LTB4 >12-epi-LTB4 >LTB5 >LTB3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7796R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7796R-HRP
Lokale Artikelnummer::
BOSSBS-7796R-HRP
Beschreibung:
This gene encodes a kinetochore protein that functions aspart of the minichromosome instability-12 centromere complex. Theencoded protein is required for proper kinetochore assembly andprogression through the cell cycle. Alternative splicing results inmultiple transcript variants. [provided by RefSeq, Feb 2009].
VE:
1 * 100 µl
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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.
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