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Artikel-Nr:
(BOSSBS-15140R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15140R-CY3
Lokale Artikelnummer::
BOSSBS-15140R-CY3
Beschreibung:
C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15125R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15125R-FITC
Lokale Artikelnummer::
BOSSBS-15125R-FITC
Beschreibung:
C22orf37 (chromosome 22 open reading frame 37), also known as FLJ40542, is a 170 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8079R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8079R-CY5
Lokale Artikelnummer::
BOSSBS-8079R-CY5
Beschreibung:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15125R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15125R-A350
Lokale Artikelnummer::
BOSSBS-15125R-A350
Beschreibung:
C22orf37 (chromosome 22 open reading frame 37), also known as FLJ40542, is a 170 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9440R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9440R-A680
Lokale Artikelnummer::
BOSSBS-9440R-A680
Beschreibung:
MTA1 is a component of the NURD (nucleosome remodeling and histone deacetylation) complex, which is associated with ATP-dependent chromatin-remodeling and histone deacetylase activity. MTA1 functions in conjunction with other components of NURD to mediate transcriptional repression as it facilitates the association of repressor molecules with the chromatin. Structurally, MTA1 contains a single SH3-binding motif and a zinc finger domain, along with a region similar to the co-repressor protein N-Cor. MTA1 is normally expressed at low levels in various tissues and is more highly expressed in testis. Overexpression of MTA1 correlates with tumour invasion and metastasis in various carcinomas including colorectal, gastrointestinal and breast carcinomas. Elevation of MTA1 levels in these tumours appears to enhance the metastases to lymph nodes, increase mammary cell motility and potentiate growth, and therefore may be an indicator for assessing the potential malignancies of various tumours. A similar protein, MTA2, also designated MTA1-L1 (MTA1-like protein 1), shares more than 55% sequence homology with MTA1 and is ubiquitously expressed.
VE:
1 * 100 µl
Artikel-Nr:
(PPSA3590210)
Lieferant:
PFENNIG REINIGUNGSTECHNIK
Hersteller-Artikelnummer::
3590210
Lokale Artikelnummer::
PPSA3590210
Beschreibung:
Squeegee mops and handles for hygienically sensitive areas.
VE:
Artikel-Nr:
(APOSOR322494-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR322494-100G
Lokale Artikelnummer::
APOSOR322494-100G
Beschreibung:
Diethylentriamin
VE:
1 * 100 g
Artikel-Nr:
(MEMMHCP50)
Lieferant:
MEMMERT
Hersteller-Artikelnummer::
HCP50
Lokale Artikelnummer::
MEMMHCP50
Beschreibung:
Feuchtekammern mit Innenkammer und Gehäuse aus korrosionsfestem Edelstahl für Langzeit-Klimaprüfungen bei konstanter Temperatur und Feuchte. Ideal für die Bereiche Lebensmittelverarbeitung, Kosmetika, Pharmazie, Biotechnologie und Elektronik. Das Gerät besitzt ein Autodiagnosesystem mit Fehleranzeige zur Temperatur- und Feuchteregelung. Die Arbeitskammer wird an allen sechs Seiten aufgeheizt. Zusammen mit der elektronischen Feuchteregelung beugt dies der Kondensatbildung in der Kammer vor. Aus einem externen 2,5-Liter-Behälter wird mit einer selbstansaugenden Pumpe destilliertes Wasser zugeführt. Interner 1024-kB-Protokollspeicher (Ringpuffer) für alle relevanten Daten, Kapazität für etwa drei Monate bei Intervallen von einer Minute. GLP/GMP-Konformität wird durch die USB-Schnittstelle und die „Celsius“ Software für Programmierung und Dokumentation gewährleistet.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-9986R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9986R-A750
Lokale Artikelnummer::
BOSSBS-9986R-A750
Beschreibung:
C22orf36 is a 315 amino acid protein that contains two LRR (leucine-rich) repeats and exists as two alternatively spliced isoforms. C22orf36 is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chromosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukaemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15140R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15140R-A488
Lokale Artikelnummer::
BOSSBS-15140R-A488
Beschreibung:
C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD215363-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD215363-250MG
Lokale Artikelnummer::
BLDPBD215363-250MG
Beschreibung:
(2R,3R,4R,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite 97%
VE:
1 * 250 mg
Lieferant:
VWR Chemicals
Beschreibung:
Die qualitativ hochwertigen Kegel-Platte-Viskositätsstandards sind ideal für die Farb- und Lackindustrie.
Artikel-Nr:
(BOSSBS-15131R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15131R-CY5
Lokale Artikelnummer::
BOSSBS-15131R-CY5
Beschreibung:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf13 gene product has been provisionally designated C22orf13 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15132R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15132R-CY3
Lokale Artikelnummer::
BOSSBS-15132R-CY3
Beschreibung:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf15 gene product has been provisionally designated C22orf15 pending further characterization.
VE:
1 * 100 µl
Lieferant:
HAVERBOECKER
Beschreibung:
Siebschale, Edelstahl, Ø: 250 mm, Höhe: 55 mm
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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