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Methyl+5-bromo-6-fluoroindole-2-carboxylate
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Methyl+5-bromo-6-fluoroindole-2-carboxylate
Artikel-Nr:
(APOSOR302039-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR302039-1G
Lokale Artikelnummer::
APOSOR302039-1G
Beschreibung:
2,5-Dibromo-3,4-pyridinediamine
VE:
1 * 1 g
Artikel-Nr:
(APOSOR471045-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR471045-1G
Lokale Artikelnummer::
APOSOR471045-1G
Beschreibung:
2-(2-Chloro-4-nitrophenyl)acetic acid
VE:
1 * 1 g
Artikel-Nr:
(BLDPBD321610-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD321610-1G
Lokale Artikelnummer::
BLDPBD321610-1G
Beschreibung:
5-(Boc-amino)-2-fluorobenzeneboronic acid pinacol ester 98%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Methyl-5-nitrophenylboronsäure 96%
Lieferant:
Alfa Aesar
Beschreibung:
Perrheniumsäure ≥75-80%
Lieferant:
Alfa Aesar
Beschreibung:
Zink(II)tellurid ≥99,998% (Metall-Basis)
Artikel-Nr:
(APOSOR111571-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR111571-1G
Lokale Artikelnummer::
APOSOR111571-1G
Beschreibung:
2-Methylimidazo[1,2-a]pyrimidine-3-carboxylic acid
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-11399R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11399R-A750
Lokale Artikelnummer::
BOSSBS-11399R-A750
Beschreibung:
Synaptotagmins are a large family of synaptic vesicle type III integral membrane proteins that function as regulators of both exocytosis and endocytosis and are involved in neurotransmitter secretion from small secretory vesicles. Synaptotagmin XI, also known as SYT11 (Synaptotagmin-11), is a 431 amino acid protein that localizes to the membrane and is expressed ubiquitously with highest expression in brain and lung. Like other Synaptotagmin proteins, Synaptotagmin XI is involved in the calcium-dependent exocytosis of secretory vesicles and is thought to act as a calcium sensor during vesicular trafficking. Synaptotagmin XI contains two C2 domains through which it can bind either three calcium ions or the zinc-finger protein Parkin (a juvenile Parkinson's disease gene product), the latter of which causes the polyubiquitination and subsequent degradation of Synaptotagmin XI by the proteasome complex. Defects in the gene encoding Synaptotagmin XI are implicated in a number of neurological disorders, including schizophrenia and Parkinson's disease.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD132858-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD132858-1G
Lokale Artikelnummer::
BLDPBD132858-1G
Beschreibung:
H-D-Glu(OtBu)-OtBu·HCl 97%
VE:
1 * 1 g
Artikel-Nr:
(BLDPBD86009-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD86009-10G
Lokale Artikelnummer::
BLDPBD86009-10G
Beschreibung:
3-Chloro-6-piperidin-1-ylpyridazine 95%
VE:
1 * 10 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl-4-(4-fluorophenoxy)-3-nitrobenzenecarboxylate 97%
Artikel-Nr:
(112-2938)
Lieferant:
ANSELL HEALTH CARE
Hersteller-Artikelnummer::
80-600/11
Lokale Artikelnummer::
ANSE80-600/11
Beschreibung:
Diese Kevlar® Strickhandschuhe bieten eine gute Schnittfestigkeit und mechanische Beständigkeit.
VE:
1 * 1 PAAR
Artikel-Nr:
(BOSSBS-11607R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11607R-CY3
Lokale Artikelnummer::
BOSSBS-11607R-CY3
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. LRRC54 (leucine-rich repeat-containing protein 54), also known as tsukushin, TSKU or E2-induced gene 4 protein (E2IG4), is a 353 amino acid secreted protein that likely localizes to the cell membrane and extracellular compartments. Involved in extracellular secretion and intracellular transport, LRRC54 can be induced by 17-beta-estradiol. Containing nine LRR repeat and a cleavable signal peptide, the gene encoding LRRC54 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9933R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9933R-A680
Lokale Artikelnummer::
BOSSBS-9933R-A680
Beschreibung:
PTD015 is a 122 amino acid protein that belongs to the UPF0366 family. Existing as three alternatively spliced isoforms, the PTD015 gene is conserved in dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 11q14.1. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The PTD015 gene product has been provisionally designated PTD015 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11607R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11607R
Lokale Artikelnummer::
BOSSBS-11607R
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. LRRC54 (leucine-rich repeat-containing protein 54), also known as tsukushin, TSKU or E2-induced gene 4 protein (E2IG4), is a 353 amino acid secreted protein that likely localizes to the cell membrane and extracellular compartments. Involved in extracellular secretion and intracellular transport, LRRC54 can be induced by 17-beta-estradiol. Containing nine LRR repeat and a cleavable signal peptide, the gene encoding LRRC54 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9933R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9933R-A750
Lokale Artikelnummer::
BOSSBS-9933R-A750
Beschreibung:
PTD015 is a 122 amino acid protein that belongs to the UPF0366 family. Existing as three alternatively spliced isoforms, the PTD015 gene is conserved in dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 11q14.1. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The PTD015 gene product has been provisionally designated PTD015 pending further characterisation.
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.
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