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4-Amino-1,5-dimethylimidazole+hydrochloride
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4-Amino-1,5-dimethylimidazole+hydrochloride
Artikel-Nr:
(APOSPC430558-500MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC430558-500MG
Lokale Artikelnummer::
APOSPC430558-500MG
Beschreibung:
2,3,3-Trifluoro-1,4-benzodioxen-5-ol
VE:
1 * 500 mg
Artikel-Nr:
(APOSOR510146-100MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR510146-100MG
Lokale Artikelnummer::
APOSOR510146-100MG
Beschreibung:
2-Methylpiperidine-2-carboxylic acid hydrochloride ≥98%
VE:
1 * 100 mg
Artikel-Nr:
(BRDY062390)
Lieferant:
Brady
Hersteller-Artikelnummer::
062390
Lokale Artikelnummer::
BRDY062390
Beschreibung:
Printable, permanent polyester labels for thermal transfer printers. Ultra-aggressive adhesive designed for powder coated surfaces, on angled and curved surfaces.
VE:
1 * 1 Rolle
Lieferant:
Alfa Aesar
Beschreibung:
Praseodymium(III) acetate hydrate ≥99,9% (REO, Basis der Oxide der Metalle der seltenen Erden)
Artikel-Nr:
(BOSSBS-11822R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-A680
Lokale Artikelnummer::
BOSSBS-11822R-A680
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyses 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
Lieferant:
VWR Collection
Beschreibung:
Eine Auswahl an binokularen und trinokularen Stereo-Zoom-Mikroskopköpfen für grundlegende oder fortgeschrittenere Anforderungen.
Lieferant:
SORVALL
Beschreibung:
BIOLink Adapter für H-12000 Rotor
Artikel-Nr:
(BLDPBD293174-100G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD293174-100G
Lokale Artikelnummer::
BLDPBD293174-100G
Beschreibung:
(S)-2-Amino-3,3-dimethylbutanamide hydrochloride 98%
VE:
1 * 100 g
Artikel-Nr:
(BLDPBD260421-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD260421-250MG
Lokale Artikelnummer::
BLDPBD260421-250MG
Beschreibung:
7-Bromo-1-methylquinolin-2(1H)-one 95%
VE:
1 * 250 mg
Lieferant:
Alfa Aesar
Beschreibung:
Cobaltdisilicid ≥99% (Metall-Basis)
Lieferant:
Alfa Aesar
Beschreibung:
Nile blue A
Lieferant:
WTW
Beschreibung:
<B>TetraCon® 325, TetraCon® V</B> and <B>KLE 325</B> are suitable for on-site measurements in rivers, lakes and wastewater, fish farming, ground water measurements and applications in water laboratories.
Artikel-Nr:
(BOSSBS-6987R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-FITC
Lokale Artikelnummer::
BOSSBS-6987R-FITC
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, 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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6987R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-A555
Lokale Artikelnummer::
BOSSBS-6987R-A555
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, 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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6987R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-CY5
Lokale Artikelnummer::
BOSSBS-6987R-CY5
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, 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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6987R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-CY3
Lokale Artikelnummer::
BOSSBS-6987R-CY3
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, 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.
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.
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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