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Methylpyrazolo[1,5-a]pyridin-3-carboxylat
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Methylpyrazolo[1,5-a]pyridin-3-carboxylat
Artikel-Nr:
(BOSSBS-13505R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13505R-HRP
Lokale Artikelnummer::
BOSSBS-13505R-HRP
Beschreibung:
GPCR2037 is a G protein-coupled receptor that undergoes weak activation by Galanin and is most abundant in the central nervous system (CNS), where it appears to be critical for development. During embryonal development the expression of GPCR2037 is widespread in the nervous system (dorsal thalamus, striatum, locus coeruleus and hindbrain nuclei). GPCR2037 in the CNS of 7- and 15-day-old mouse embryos can localize to the habenular complex. Low levels of GPCR2037 are detectable in testis, liver, kidney and stomach. In addition to GPCR2037, Galanin mediates its effects through receptor subtypes GALR1, 2 and 3. Galanin ligand exerts anxiolytic actions via GALR receptors under conditions of high stress. Galanin coexists with norepinephrine and serotonin in neural systems that mediate emotion.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13505R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13505R-CY3
Lokale Artikelnummer::
BOSSBS-13505R-CY3
Beschreibung:
GPCR2037 is a G protein-coupled receptor that undergoes weak activation by Galanin and is most abundant in the central nervous system (CNS), where it appears to be critical for development. During embryonal development the expression of GPCR2037 is widespread in the nervous system (dorsal thalamus, striatum, locus coeruleus and hindbrain nuclei). GPCR2037 in the CNS of 7- and 15-day-old mouse embryos can localize to the habenular complex. Low levels of GPCR2037 are detectable in testis, liver, kidney and stomach. In addition to GPCR2037, Galanin mediates its effects through receptor subtypes GALR1, 2 and 3. Galanin ligand exerts anxiolytic actions via GALR receptors under conditions of high stress. Galanin coexists with norepinephrine and serotonin in neural systems that mediate emotion.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13505R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13505R-FITC
Lokale Artikelnummer::
BOSSBS-13505R-FITC
Beschreibung:
GPCR2037 is a G protein-coupled receptor that undergoes weak activation by Galanin and is most abundant in the central nervous system (CNS), where it appears to be critical for development. During embryonal development the expression of GPCR2037 is widespread in the nervous system (dorsal thalamus, striatum, locus coeruleus and hindbrain nuclei). GPCR2037 in the CNS of 7- and 15-day-old mouse embryos can localize to the habenular complex. Low levels of GPCR2037 are detectable in testis, liver, kidney and stomach. In addition to GPCR2037, Galanin mediates its effects through receptor subtypes GALR1, 2 and 3. Galanin ligand exerts anxiolytic actions via GALR receptors under conditions of high stress. Galanin coexists with norepinephrine and serotonin in neural systems that mediate emotion.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13482R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13482R-A647
Lokale Artikelnummer::
BOSSBS-13482R-A647
Beschreibung:
The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The protein encoded by this gene is a member of the golgin family of proteins, whose members localize to the Golgi. This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, that are greather than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosome rearrangements that underlie genomic disease. The protein encoded by this gene is thought to be a functional golgin protein while the majority of the related copies of this gene are thought to be transcribed pseudogenes.
VE:
1 * 100 µl
Artikel-Nr:
(MOLE15293583-5G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
15293583-5G
Lokale Artikelnummer::
MOLE15293583-5G
Beschreibung:
2,6-Di-tert-butylpyridin
VE:
1 * 5 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
COMBI-BLOCKS
Beschreibung:
4-Pyridinboronsäure Hydrochlorid
Artikel-Nr:
(MAYBCC13701-0001)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
CC13701-0001
Lokale Artikelnummer::
MAYBCC13701-0001
Beschreibung:
2-(3-Pyridinyl)-4-thiazolcarbonsäure
VE:
1 * 1 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(H27052.03)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
H27052.03
Lokale Artikelnummer::
ALFAH27052.03
Beschreibung:
(S)-1-(tert-Butoxycarbonyl)-4,4-difluoro-2-pyrrolidinecarboxylic acid ≥97%
VE:
1 * 1 g
Artikel-Nr:
(SIALW370908-5KG-K)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
W370908-5KG-K
Lokale Artikelnummer::
SIALW370908-5KG-K
Beschreibung:
Methylnicotinat, Sigma-Aldrich®
VE:
1 * 5 kg
Artikel-Nr:
(PROOMM0549.00)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
MM0549.00
Lokale Artikelnummer::
PROOMM0549.00
Beschreibung:
Methylnicotinat
VE:
1 * 500 mg
Lieferant:
Sigma-Aldrich
Beschreibung:
Chlor(1,5-cyclooctadien)rhodium(I) dimer, Sigma-Aldrich®
Lieferant:
Sigma-Aldrich
Beschreibung:
Methylnicotinat, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-15126R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15126R-FITC
Lokale Artikelnummer::
BOSSBS-15126R-FITC
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11785R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11785R-FITC
Lokale Artikelnummer::
BOSSBS-11785R-FITC
Beschreibung:
Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15126R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15126R-A750
Lokale Artikelnummer::
BOSSBS-15126R-A750
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11785R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11785R-A350
Lokale Artikelnummer::
BOSSBS-11785R-A350
Beschreibung:
Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
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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