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Ethyl+5-hydroxypyrazolo[1,5-a]pyrimidine-3-carboxylate
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Ethyl+5-hydroxypyrazolo[1,5-a]pyrimidine-3-carboxylate
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-(Phenylsulfonyl)pyrrolidin
Artikel-Nr:
(9099.0100)
Lieferant:
Avantor
Lokale Artikelnummer::
BAKR9099.0100
Beschreibung:
Natriumazid, BAKER, Laborreagens, J.T.Baker®
VE:
1 * 100 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Glyoxal dimethyl acetal 60% in wässriger Lösung
Artikel-Nr:
(APOSOR54632-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR54632-25G
Lokale Artikelnummer::
APOSOR54632-25G
Beschreibung:
Bis(2-pyridylmethyl)amine 97%
VE:
1 * 25 g
Artikel-Nr:
(BOSSBS-11489R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11489R-FITC
Lokale Artikelnummer::
BOSSBS-11489R-FITC
Beschreibung:
TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11489R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11489R-A350
Lokale Artikelnummer::
BOSSBS-11489R-A350
Beschreibung:
TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11489R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11489R-CY3
Lokale Artikelnummer::
BOSSBS-11489R-CY3
Beschreibung:
TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8112R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8112R-A350
Lokale Artikelnummer::
BOSSBS-8112R-A350
Beschreibung:
CCDC117 is a 279 amino acid protein that is expressed as multiple alternatively spliced isoforms and is encoded by a gene which maps to human chromosome 22. Chromosome 22 houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8112R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8112R-A488
Lokale Artikelnummer::
BOSSBS-8112R-A488
Beschreibung:
CCDC117 is a 279 amino acid protein that is expressed as multiple alternatively spliced isoforms and is encoded by a gene which maps to human chromosome 22. Chromosome 22 houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8112R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8112R-A750
Lokale Artikelnummer::
BOSSBS-8112R-A750
Beschreibung:
CCDC117 is a 279 amino acid protein that is expressed as multiple alternatively spliced isoforms and is encoded by a gene which maps to human chromosome 22. Chromosome 22 houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
VE:
1 * 100 µl
Lieferant:
Spectrum Laboratories
Beschreibung:
MWCO 1 - 50 kD, regenerierte Cellulose.
Artikel-Nr:
(BOSSBS-9369R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9369R-A647
Lokale Artikelnummer::
BOSSBS-9369R-A647
Beschreibung:
ODF3B, also known as ODF3L3 (outer dense fiber protein 3-like protein 3), is a 253 amino acid protein belonging to the ODF3 family. Existing as two isoforms produced by alternative splicing, ODF3B contains one DUF1309 repeat. The gene that encodes ODF3B maps to human chromosome 22, which 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.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Nitrophenyl selenocyanate
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
1,4-Bis(2-hydroxyisopropyl)benzol 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Methoxy-4-methylbenzaldehyde
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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