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2-Chloro-4,6-dimethylpyrimidine
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2-Chloro-4,6-dimethylpyrimidine
Artikel-Nr:
(BOSSBS-8225R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8225R-A488
Lokale Artikelnummer::
BOSSBS-8225R-A488
Beschreibung:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which 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' tumors, 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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11399R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11399R-A680
Lokale Artikelnummer::
BOSSBS-11399R-A680
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:
(BOSSBS-9659R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-A750
Lokale Artikelnummer::
BOSSBS-9659R-A750
Beschreibung:
With approximately 135 million base pairs and 1,400 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 FAM76B gene product has been provisionally designated FAM76B pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6758R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6758R-A750
Lokale Artikelnummer::
BOSSBS-6758R-A750
Beschreibung:
Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 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, while Wilms' tumors, 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-encoded genes.
VE:
1 * 100 µl
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
Methyl 3-chloro-4-methylthiophene-2-carboxylate 98%
Artikel-Nr:
(BLDPBD257622-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD257622-1G
Lokale Artikelnummer::
BLDPBD257622-1G
Beschreibung:
5,6-Dibromo-2-pyridinamine 97%
VE:
1 * 1 g
Lieferant:
Alfa Aesar
Beschreibung:
Mucobromsäure ≥98%
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Diese Nylonhandschuhe mit Nitril-Beschichtung an der Handfläche verfügen über die Ansell Grip Technology™. Mikroskopische Kanäle in der Beschichtung leiten das Öl ab und ermöglichen so einen sicheren Kontakt zwischen Handschuh und Oberfläche. Dies ermöglicht dem Träger den sicheren Umgang mit kleinen und mittelgroßen, öligen Komponenten.
Artikel-Nr:
(ANSE48-205/11)
Lieferant:
ANSELL HEALTH CARE
Hersteller-Artikelnummer::
48-205/11
Lokale Artikelnummer::
ANSE48-205/11
Beschreibung:
An affordable solution for demanding extraction jobs.
VE:
1 * 12 PAAR
Artikel-Nr:
(BOSSBS-11607R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11607R-HRP
Lokale Artikelnummer::
BOSSBS-11607R-HRP
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3'-Fluorbiphenyl-2-carbonsäure
Lieferant:
VWR Collection
Beschreibung:
Diese Pipetten zeichnen sich durch hohe Genauigkeit, Präzision und Robustheit sowie ein modernes ergonomisches Design aus.
Lieferant:
Hach
Beschreibung:
UV/Visible spectrophotometers with radio frequency (RFID) technology to ensure high speed wavelength scanning across the UV and visible spectrum.
Artikel-Nr:
(1076261.)
Lieferant:
USP
Hersteller-Artikelnummer::
1076261
Lokale Artikelnummer::
USPH1076261
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 20 mg
Artikel-Nr:
(ANSE48-102/11)
Lieferant:
ANSELL HEALTH CARE
Hersteller-Artikelnummer::
48-102/11
Lokale Artikelnummer::
ANSE48-102/11
Beschreibung:
Seamless knitted polyamide gloves with PU coating on palm and fingertips.
VE:
1 * 12 PAAR
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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