Imidazo[1,2-b]pyridazin
Artikel-Nr:
(BOSSBS-3743R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3743R
Lokale Artikelnummer::
BOSSBS-3743R
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-12920R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12920R
Lokale Artikelnummer::
BOSSBS-12920R
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-15130R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R
Lokale Artikelnummer::
BOSSBS-15130R
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-11324R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11324R-CY5
Lokale Artikelnummer::
BOSSBS-11324R-CY5
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:
(442-0087)
Lieferant:
COWIE
Hersteller-Artikelnummer::
001.3013
Lokale Artikelnummer::
COWI001.3013
Beschreibung:
Magnetrhrstbchen-Set, Typ: UK 3, Inhalt: 12 elliptische Rhrstbchen und 1 Entferner 1 * 1 ST
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-0394R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0394R
Lokale Artikelnummer::
BOSSBS-0394R
Beschreibung:
This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene may play a role in the regulation of cartilage differentiation. It could also be involved in chondrodysplasias or other cartilage disorders.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR88770-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR88770-1G
Lokale Artikelnummer::
APOSOR88770-1G
Beschreibung:
1-tert-Butyl 2-methyl (2S)-3,3-dimethyl-4-oxopyrrolidine-1,2-dicarboxylate 1g pack 1 * 1 g
VE:
1 * 1 g
New Product
Artikel-Nr:
(APOSOR87038-500MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR87038-500MG
Lokale Artikelnummer::
APOSOR87038-500MG
Beschreibung:
1-tert-Butyl 2-methyl 2-(chloromethyl)pyrrolidine-1,2-dicarboxylate 500mg pack 1 * 500 mg
VE:
1 * 500 mg
New Product
Artikel-Nr:
(BOSSBS-12919R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12919R
Lokale Artikelnummer::
BOSSBS-12919R
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:
(APOSOR91796-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR91796-5G
Lokale Artikelnummer::
APOSOR91796-5G
Beschreibung:
1-(tert-Butyl) 2-methyl (R)-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate 5g pack 1 * 5 g
VE:
1 * 5 g
New Product
Artikel-Nr:
(ICNA117022160)
Lieferant:
MP Biomedicals
Hersteller-Artikelnummer::
117022160
Lokale Artikelnummer::
ICNA117022160
Beschreibung:
MPure™ Total RNA Extraction Kit is used with the MPure-12™ Automated Nucleic Acid Purification System for extraction of total RNA from whole blood, blood cells, animal tissue, plant tissue, yeast or cultured cells and viral RNA from human biological specimens such as serum, plasma, and other cell-free fluids.
VE:
1 * 1 KIT
Lieferant:
AGILENT
Beschreibung:
The AdEasy Virus Purification Kit allows the purification and concentration of Adenovirus (from Ad5 strains) with Sartobind® syringe filters containing an ion exchange membrane adsorber that selectively binds adenoviral particles. Once bound, viral particles can be further purified by washing away nonspecifically-bound proteins before elution. Concentrated and purified viral particles can be obtained in 2 to 3 hours, in contrast to traditional CsCl gradient centrifugation which typically takes 12 to 48 hours.
Artikel-Nr:
(BOSSBS-11406R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11406R-CY5
Lokale Artikelnummer::
BOSSBS-11406R-CY5
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:
(BOSSBS-12919R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12919R-A647
Lokale Artikelnummer::
BOSSBS-12919R-A647
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-15130R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-CY3
Lokale Artikelnummer::
BOSSBS-15130R-CY3
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-9982R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9982R-A750
Lokale Artikelnummer::
BOSSBS-9982R-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 C21orf87 gene product has been provisionally designated C21orf87 pending further characterisation.
VE:
1 * 100 µl
Preis auf Anfrage
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