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2-Chloro-1-ethyl-1H-imidazole
Artikel-Nr:
(BOSSBS-8130R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-A750
Lokale Artikelnummer::
BOSSBS-8130R-A750
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-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-HRP
Lokale Artikelnummer::
BOSSBS-8130R-HRP
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-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-CY3
Lokale Artikelnummer::
BOSSBS-8130R-CY3
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:
(ACRO195410010)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
195410010
Lokale Artikelnummer::
ACRO195410010
Beschreibung:
Platin(II)bromid 98%
VE:
1 * 1 g
Lieferant:
Alfa Aesar
Beschreibung:
4-(Methoxycarbonyl)phenylboronsäure ≥97%
Artikel-Nr:
(BLDPBD01128756-100)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01128756-100
Lokale Artikelnummer::
BLDPBD01128756-100
Beschreibung:
4,4'-(Piperazine-1,4-diyl)dianiline 98%
VE:
1 * 100 mg
Artikel-Nr:
(BLDPBD268496-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD268496-25G
Lokale Artikelnummer::
BLDPBD268496-25G
Beschreibung:
2,5-Dibromothiophene-3,4-dicarboxylic acid 95%
VE:
1 * 25 g
Artikel-Nr:
(BOSSBS-5049R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R
Lokale Artikelnummer::
BOSSBS-5049R
Beschreibung:
Catalyzes the first step in the oxidation of the side chain of sterol intermediates; the 27-hydroxylation of 5-beta-cholestane-3-alpha,7-alpha,12-alpha-triol. Has also a vitamin D3-25-hydroxylase activity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9950R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9950R-A750
Lokale Artikelnummer::
BOSSBS-9950R-A750
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 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. The C12orf50 gene product has been provisionally designated C12orf50 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11003R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-A555
Lokale Artikelnummer::
BOSSBS-11003R-A555
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 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. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11003R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-A647
Lokale Artikelnummer::
BOSSBS-11003R-A647
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 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. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9952R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9952R-A680
Lokale Artikelnummer::
BOSSBS-9952R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 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. The C12orf54 gene product has been provisionally designated C12orf54 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9955R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9955R-A680
Lokale Artikelnummer::
BOSSBS-9955R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 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. The LOC387856 gene product has been provisionally designated LOC387856 pending further characterisation.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Pentane-2,3,4-trione 3-oxime
Artikel-Nr:
(BLDPBD15063-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD15063-10G
Lokale Artikelnummer::
BLDPBD15063-10G
Beschreibung:
3,4-Difluorbenzophenon 98%
VE:
1 * 10 g
Artikel-Nr:
(BOSSBS-12163R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12163R-CY7
Lokale Artikelnummer::
BOSSBS-12163R-CY7
Beschreibung:
CAPS2 is a 557 amino acid calcium-binding protein that is abundantly expressed, with highest expression found in placenta, testis, colon, lung and brain. CAPS2 contains three EF-hand domains and exists as three alternatively spliced isoforms. Suggested to play a role in large dense-core vesicle (LDCV) exocytosis, CAPS2 is encoded by a gene that 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
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.
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