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2-Chloro-4,5-difluorobenzamide
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2-Chloro-4,5-difluorobenzamide
Artikel-Nr:
(BLDPBD159069-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD159069-250MG
Lokale Artikelnummer::
BLDPBD159069-250MG
Beschreibung:
4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid 98%
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-Chloro-4-(1,1-difluoroethyl)-2-(trifluoromethyl)benzene 97%
Artikel-Nr:
(APOSOR6423-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR6423-1G
Lokale Artikelnummer::
APOSOR6423-1G
Beschreibung:
4-Chloro-1H-pyrazolo[3,4-d]pyrimidine 97%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Chloro-1H-indazole-3-carboxylic acid 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-(5-Chloro-1H-indazol-1-yl)ethanone 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Chloro-1-(tert-butyl)-1H-imidazole 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl-3-(2-chloro-6-fluorophenyl)-5-[2-(dimethylamino)vinyl]-4-isoxazolecarboxylate
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl-4-{[3-chloro-5-(trifluoromethyl)-2-pyridinyl]amino}butanoate
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Chloro-7-trifluoromethylquinoline-3-carboxylic acid ethyl ester
Artikel-Nr:
(BOSSBS-9716R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9716R-HRP
Lokale Artikelnummer::
BOSSBS-9716R-HRP
Beschreibung:
Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9716R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9716R-CY3
Lokale Artikelnummer::
BOSSBS-9716R-CY3
Beschreibung:
Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6471R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6471R-A350
Lokale Artikelnummer::
BOSSBS-6471R-A350
Beschreibung:
Inositol 1,4,5-triphosphate (IP3) functions as a second messenger for a myriad of extracellular stimuli including hormones, growth factors and neurotransmitters. Receptor tyrosine kinases indirectly increase the intracellular levels of IP3 through the activation of phospholipases such as phospholipase C (PLC), which convert phosphatidylinositol-4,5 bisphosphate into IP3 and diacylglycerol (DAG). The inositol 1,4,5-triphosphate receptor, IP3R, acts as an inositol triphosphate (IP3)-gated calcium release channel in a variety of cell types. Three IP3 receptor subtypes have been described and are designated IP3R-I, IP3R-II and IP3R-III. IP3R-I is the predominant IP3R subtype expressed in neuronal tissues and the central nervous system, but is also expressed at high levels in the liver.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9771R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9771R-A750
Lokale Artikelnummer::
BOSSBS-9771R-A750
Beschreibung:
C10orf88 is a 445 amino acid protein encoded by a gene that maps to human chromosome 10q26.13. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12411R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12411R-A555
Lokale Artikelnummer::
BOSSBS-12411R-A555
Beschreibung:
Prickle1 is an 831 amino acid protein that contains one PET domain and three LIM zinc-binding domains and localizes to the cytoplasm, as well as to the nuclear membrane. Expressed at higher levels in placenta and at lower levels in liver, brain, kidney, lung and pancreas, Prickle1 is thought to function as a nuclear receptor that interacts with NRSF, a silencer protein that binds the DNA sequence element NRSE (neuron-restrictive silencer element). Defects in the gene encoding Prickle1 are associated with autosomal recessive progressive myoclonic epilepsy-1B, which is characterized by quick jerks of the arms, shoulders or legs. The gene encoding Prickle1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12411R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12411R-A488
Lokale Artikelnummer::
BOSSBS-12411R-A488
Beschreibung:
Prickle1 is an 831 amino acid protein that contains one PET domain and three LIM zinc-binding domains and localizes to the cytoplasm, as well as to the nuclear membrane. Expressed at higher levels in placenta and at lower levels in liver, brain, kidney, lung and pancreas, Prickle1 is thought to function as a nuclear receptor that interacts with NRSF, a silencer protein that binds the DNA sequence element NRSE (neuron-restrictive silencer element). Defects in the gene encoding Prickle1 are associated with autosomal recessive progressive myoclonic epilepsy-1B, which is characterized by quick jerks of the arms, shoulders or legs. The gene encoding Prickle1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(15136-250MG)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
15136-250MG
Lokale Artikelnummer::
SUPL15136-250MG
Beschreibung:
Standard for determining toxic monomers released from polymers of the inner coating of cans.
VE:
1 * 250 mg
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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