2-Amino-5-ethoxy-6-methylpyridine
Artikel-Nr:
(BOSSBS-12925R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12925R-A488
Lokale Artikelnummer::
BOSSBS-12925R-A488
Beschreibung:
This protein is one of the nuclear-coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12925R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12925R-A350
Lokale Artikelnummer::
BOSSBS-12925R-A350
Beschreibung:
This protein is one of the nuclear-coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD15137-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD15137-25G
Lokale Artikelnummer::
BLDPBD15137-25G
Beschreibung:
10,11-Dihydro-11-oxodibenzo[b,f][1,4]thiazepine 98%
VE:
1 * 25 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Hydroxy-5-nitropyridin 98%
Artikel-Nr:
(APOSPC5571-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC5571-1G
Lokale Artikelnummer::
APOSPC5571-1G
Beschreibung:
1,1,3,3,3-Pentafluorpropylmethylether 97%
VE:
1 * 1 g
Lieferant:
Alfa Aesar
Beschreibung:
2-Hydroxy-5-nitropyridin ≥98%
Artikel-Nr:
(BOSSBS-8130R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-CY7
Lokale Artikelnummer::
BOSSBS-8130R-CY7
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 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
Artikel-Nr:
(BOSSBS-8130R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-A555
Lokale Artikelnummer::
BOSSBS-8130R-A555
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 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
Artikel-Nr:
(BOSSBS-8130R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-CY5
Lokale Artikelnummer::
BOSSBS-8130R-CY5
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 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
Artikel-Nr:
(BOSSBS-8130R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-A647
Lokale Artikelnummer::
BOSSBS-8130R-A647
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 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
Artikel-Nr:
(BOSSBS-8130R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-A350
Lokale Artikelnummer::
BOSSBS-8130R-A350
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 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
Artikel-Nr:
(BOSSBS-11622R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R-A350
Lokale Artikelnummer::
BOSSBS-11622R-A350
Beschreibung:
Polycystin-1L3 is a 1,732 amino acid multi-pass membrane protein that contains one PLAT domain, one GPS domain and one C-type lectin domain. Expressed at high levels in placenta and present at lower levels in lung and heart, Polycystin-1L3 is thought to function as an ion-channel regulator that may interact with Polycystin-L and play a role in heteromeric taste channels. The gene encoding Polycystin-1L3 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
(4-Iodphenyl)acetonitril ≥97%
Artikel-Nr:
(245-1227)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI245-1227
Beschreibung:
Hochwertiges, stabiles und preisgünstiges Sortiment an Hebebühnen für eine Vielzahl von Einsatzzwecken. Mit Platten aus matt gebürstetem, rostfreiem Edelstahl und mit leichtgängigem Aluminium-Scherengitter. Gummifüße sorgen für einen stabilen Stand.
VE:
1 * 1 ST
Artikel-Nr:
(H50438.06)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
H50438.06
Lokale Artikelnummer::
ALFAH50438.06
Beschreibung:
3-(3-Bromophenyl)-1H-pyrazole 98%
VE:
1 * 5 g
Preis auf Anfrage
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-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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