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(\\\\u00B1)-1,2-Pentandiol
Artikel-Nr:
(BOSSBS-3953R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3953R-CY5
Lokale Artikelnummer::
BOSSBS-3953R-CY5
Beschreibung:
Cytochrome c oxidase subunit I (COI or MTCO1) is one of three mitochondrial DNA (mtDNA) encoded subunits (MTCO1, MTCO2, MTCO3) of respiratory Complex IV. Complex IV is located within the mitochondrial inner membrane and is the third and final enzyme of the electron transport chain of mitochondrial oxidative phosphorylation. Complex IV is composed of 13 polypeptides. Subunits I, II, and III (MTCO1, MTCO2, MTCO3) are encoded by mtDNA while subunits IV, Va, Vb, VIa, VIb, VIc, VIIa, VIIb, VIIc, and VIII are nuclear encoded. Mammalian MTCO1 has 12 membrane-spanning alpha-helices (I to XII).
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
1,2-Dimethoxyethan, extra trocken über Molekularsieb 99.5% stabilisiert, AcroSeal™
Lieferant:
COMBI-BLOCKS
Beschreibung:
3,8-Dibrom-6-chlorimidazo[1,2-a]pyridin
Artikel-Nr:
(BOSSBS-13715R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13715R-CY7
Lokale Artikelnummer::
BOSSBS-13715R-CY7
Beschreibung:
The cadherins are a family of Ca++-dependent adhesion molecules that function to mediate cell-cell binding critical to the maintenance of tissue structure and morpho-genesis (1-4). Cadherins each contain a large extracellular domain at the amino terminus, which is characterized by a series of five homologous repeats, the most distal of which is thought to be responsible for binding specificity (5,6). The relatively short carboxy terminal, intracellular domain interacts with a variety of cytoplasmic proteins, including catenin b, to regulate cadherin function (7). BR-cadherin (for brain-cadherin, also designated cadherin-12 or N-cadherin 2) is expressed specifically in neurons in the central nervous system and is thought to be involved in neuronal development (8).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15188R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15188R
Lokale Artikelnummer::
BOSSBS-15188R
Beschreibung:
C4orf12 (chromosome 4 open reading frame 12) is a 926 amino acid single-pass membrane protein that exists as two isoforms. The gene encoding C4orf21 maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
3,4-Dihydroxy-3-cyclobuten-1,2-dion
Artikel-Nr:
(BOSSBS-12919R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12919R-A555
Lokale Artikelnummer::
BOSSBS-12919R-A555
Beschreibung:
This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9974R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9974R-A750
Lokale Artikelnummer::
BOSSBS-9974R-A750
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf56 gene product has been provisionally designated C21orf56 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15130R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-A750
Lokale Artikelnummer::
BOSSBS-15130R-A750
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12919R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12919R-CY3
Lokale Artikelnummer::
BOSSBS-12919R-CY3
Beschreibung:
This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9978R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9978R-A750
Lokale Artikelnummer::
BOSSBS-9978R-A750
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf58 gene product has been provisionally designated C21orf58 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11324R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11324R-A350
Lokale Artikelnummer::
BOSSBS-11324R-A350
Beschreibung:
Nova-1 and Nova-2 are members of a superfamily of protein regulators of RNA metabolism in neurons. Both are nuclear RNA binding proteins with K homology motifs, conserved protein sequences which bind to RNA (1,2). Nova proteins, normally sequestered in the central nervous system, are expressed by systemic tumors in patients with the autoimmune disorder paraneoplastic opsoclonus-myoclonus ataxia (POMA) (3,4). Nova-1 is expressed in the hindbrain and ventral spinal cord and Nova-2 is expressed in the neocortex and hippocampus (4). Nova-1 is necessary for regulating neuron-specific alternative splicing of the glycine receptor Alpha2 pre-mRNA (5).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15130R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-HRP
Lokale Artikelnummer::
BOSSBS-15130R-HRP
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11406R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11406R-CY7
Lokale Artikelnummer::
BOSSBS-11406R-CY7
Beschreibung:
GIOT-1 is a 563 amino acid protein belonging to the Krüppel C2H2-type zinc-finger protein family. Localized to the nucleus, GIOT-1 is widely expressed in tissues, with highest levels in liver, kidney, small intestine, pancreas and thymus. GIOT-1 contains 12 C2H2-type zinc fincers and one KRAB domain. Because the KRAB domain functions as a transcriptional repressor when attached to the template DNA, GIOT-1 is thought to be involved in transcriptional regulation. The gene encoding GIOT-1 is localized to chromosome 19q13.12 and two isoforms of GIOT-1 exist as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(SIAL288365-50G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
288365-50G
Lokale Artikelnummer::
SIAL288365-50G
Beschreibung:
1,2-Difluor-4-nitrobenzol, Sigma-Aldrich®
VE:
1 * 50 g
Artikel-Nr:
(BOSSBS-11324R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11324R-CY7
Lokale Artikelnummer::
BOSSBS-11324R-CY7
Beschreibung:
Nova-1 and Nova-2 are members of a superfamily of protein regulators of RNA metabolism in neurons. Both are nuclear RNA binding proteins with K homology motifs, conserved protein sequences which bind to RNA (1,2). Nova proteins, normally sequestered in the central nervous system, are expressed by systemic tumors in patients with the autoimmune disorder paraneoplastic opsoclonus-myoclonus ataxia (POMA) (3,4). Nova-1 is expressed in the hindbrain and ventral spinal cord and Nova-2 is expressed in the neocortex and hippocampus (4). Nova-1 is necessary for regulating neuron-specific alternative splicing of the glycine receptor Alpha2 pre-mRNA (5).
VE:
1 * 100 µl
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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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