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5-Chloronaphthalene-2-sulphonyl+chloride
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5-Chloronaphthalene-2-sulphonyl+chloride
Artikel-Nr:
(BOSSBS-9604R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9604R-CY3
Lokale Artikelnummer::
BOSSBS-9604R-CY3
Beschreibung:
Transcription factor 25 acts as a transcriptional repressor. It has been shown to repress transcription of SRF in vitro and hence may play a role in heart development.Transcription factor 25, is a 676 amino acid protein that plays a role in cell death. A member of the TCF25 family, Nulp1 utilizes its C-terminus to mediate transcriptional repression of SRF in vitro, and interacts with XIAP. Nulp1 localizes primarily to the nucleus but is also found in cytosol. Widely expressed, Nulp1 is found at high levels in embryonic brain and adult heart. The gene encoding Nulp1 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
Artikel-Nr:
(BOSSBS-9604R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9604R-A555
Lokale Artikelnummer::
BOSSBS-9604R-A555
Beschreibung:
Transcription factor 25 acts as a transcriptional repressor. It has been shown to repress transcription of SRF in vitro and hence may play a role in heart development.Transcription factor 25, is a 676 amino acid protein that plays a role in cell death. A member of the TCF25 family, Nulp1 utilizes its C-terminus to mediate transcriptional repression of SRF in vitro, and interacts with XIAP. Nulp1 localizes primarily to the nucleus but is also found in cytosol. Widely expressed, Nulp1 is found at high levels in embryonic brain and adult heart. The gene encoding Nulp1 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
Artikel-Nr:
(BLDPBD6502-100G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD6502-100G
Lokale Artikelnummer::
BLDPBD6502-100G
Beschreibung:
1-(4-Pyridinyl)aceton 98%
VE:
1 * 100 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-Chlor-3,5-dimethoxybenzol 98%
Artikel-Nr:
(BLDPBD6114-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD6114-25G
Lokale Artikelnummer::
BLDPBD6114-25G
Beschreibung:
5-Chlor-2-methoxybenzoesäure 95%
VE:
1 * 25 g
Artikel-Nr:
(BWRLBS4860)
Lieferant:
Bioworld Technology
Hersteller-Artikelnummer::
BS4860
Lokale Artikelnummer::
BWRLBS4860
Beschreibung:
Synthetic phosphopeptide derived from human PIN1 around the phosphorylation site of Serine 16.
VE:
1 * 100 µG
Artikel-Nr:
(BLDPBD01200315-50M)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01200315-50M
Lokale Artikelnummer::
BLDPBD01200315-50M
Beschreibung:
GRL0617 98%
VE:
1 * 50 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Chloropyrimidin-2(1H)-one 98%
Artikel-Nr:
(APOSOR345045-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR345045-1G
Lokale Artikelnummer::
APOSOR345045-1G
Beschreibung:
2-Amino-6-methylpyridin-3-ol 97%
VE:
1 * 1 g
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
Artikel-Nr:
(BOSSBS-9632R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9632R-HRP
Lokale Artikelnummer::
BOSSBS-9632R-HRP
Beschreibung:
PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.
VE:
1 * 100 µl
Artikel-Nr:
(ACRO291660050)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
291660050
Lokale Artikelnummer::
ACRO291660050
Beschreibung:
Appearance: Clear orange-brown Liquid
VE:
1 * 5 mL
Artikel-Nr:
(BOSSBS-9632R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9632R-A555
Lokale Artikelnummer::
BOSSBS-9632R-A555
Beschreibung:
PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11622R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R-A680
Lokale Artikelnummer::
BOSSBS-11622R-A680
Beschreibung:
Polycystin-1L3 is a 1732 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 characterised 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
Artikel-Nr:
(BOSSBS-11622R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R-A647
Lokale Artikelnummer::
BOSSBS-11622R-A647
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:
DWK Life Sciences
Beschreibung:
DURAN®, Borosilikatglas 3.3, klar. Dickwandig, mechanisch besonders widerstandsfähig.
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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