1,3-Bis(3-aminopropyl)tetramethyldisiloxane
Artikel-Nr:
(22955.30)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
22955.30
Lokale Artikelnummer::
ALFA22955.30
Beschreibung:
Tungsten carbide cobalt ≥99% (Metall-Basis)
VE:
1 * 250 g
Artikel-Nr:
(MOLEM73820015)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M73820015
Lokale Artikelnummer::
MOLEM73820015
Beschreibung:
3-Picolylchlorid Hydrochlorid
VE:
1 * 25 g
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Artikel-Nr:
(MOLEM44972750)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M44972750
Lokale Artikelnummer::
MOLEM44972750
Beschreibung:
4-Picolylchlorid Hydrochlorid
VE:
1 * 25 g
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Artikel-Nr:
(MOLEM45320712)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M45320712
Lokale Artikelnummer::
MOLEM45320712
Beschreibung:
5-Methoxytryptamin Hydrochlorid
VE:
1 * 1 g
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Lieferant:
Alfa Aesar
Beschreibung:
Metoclopramide hydrochloride
Artikel-Nr:
(662-2020)
Lieferant:
WTW
Hersteller-Artikelnummer::
103791
Lokale Artikelnummer::
WTWA103791
Beschreibung:
IDS ORP electrodes are used to measure oxidation or reduction potentials in aqueous solutions - with integrated temperature sensor.
VE:
1 * 1 ST
Artikel-Nr:
(BLDPBD74083-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD74083-1G
Lokale Artikelnummer::
BLDPBD74083-1G
Beschreibung:
6-Fluor-2-pyridincarbonitril 97%
VE:
1 * 1 g
Artikel-Nr:
(PROOBP468)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
BP468
Lokale Artikelnummer::
PROOBP468
Beschreibung:
Dopamin Hydrochlorid
VE:
1 * 100 mg
Artikel-Nr:
(SPCMC2127-25KGBL)
Lieferant:
Spectrum Chemical
Hersteller-Artikelnummer::
C2127-25KGBL
Lokale Artikelnummer::
SPCMC2127-25KGBL
Beschreibung:
Cyclohexylamine Hydrochloride is an organic compound that is an aliphatic amine. The compound is a high-melting solid. Cyclohexylamine hydrochloride is used as an intermediate in the synthesis of other organic compounds.
VE:
1 * 25 kg
Lieferant:
FLUOROCHEM
Beschreibung:
4-Pyridinboronsäure Hydrochlorid
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Acetamido-5-carboxyphenylboronsäure 98%
Artikel-Nr:
(BOSSBS-8076R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-A647
Lokale Artikelnummer::
BOSSBS-8076R-A647
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localized, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognized for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8076R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-A488
Lokale Artikelnummer::
BOSSBS-8076R-A488
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localized, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognized for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8076R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-A750
Lokale Artikelnummer::
BOSSBS-8076R-A750
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localized, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognized for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8076R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-CY7
Lokale Artikelnummer::
BOSSBS-8076R-CY7
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localised, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognised for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localised genes.
VE:
1 * 100 µl
Lieferant:
FLUOROCHEM
Beschreibung:
Acetamidin Hydrochlorid
Preis auf Anfrage
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