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2-Amino-5-methyl-3-nitropyridin
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2-Amino-5-methyl-3-nitropyridin
Artikel-Nr:
(BOSSBS-11009R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11009R
Lokale Artikelnummer::
BOSSBS-11009R
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 FAM83F gene product has been provisionally designated FAM83F pending further characterization.
VE:
1 * 100 µl
Lieferant:
COMBI-BLOCKS
Beschreibung:
4-Methyl-3-nitrobenzotrifluorid
Artikel-Nr:
(BOSSBS-11302R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11302R-HRP
Lokale Artikelnummer::
BOSSBS-11302R-HRP
Beschreibung:
Members of the NK-2 family of homeodomain proteins are key regulators of growth and development in several tissues, including brain, heart and pancreas. During neural development, sonic hedgehog (Shh) is known to control cell fate and mitogenesis, which is correlated with Shh dose-dependent expression of several genes, including Nkx-2.1, Nkx-2.2 and Nkx-2.9. Specifically, the Nkx-2.2 protein is responsible for directing ventral neuronal patterning in response to graded Shh signaling. In the pancreas, Nkx-2.2 is expressed in a, b and pancreatic polypeptide (PP) cells, but not in d cells. Nkx-2.2 expression is required for differentiation of pancreatic b cells, which produce insulin. Homozygous null mutations of the Nkx-2.2 gene in mice lead to severe hyperglycemia and death shortly after birth, which suggests that Nkx-2.2 may be an important therapeutic target for pancreatic diseases, including diabetes and cancer.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ninhydrin 99%
Artikel-Nr:
(ENAMEN300105228.1G)
Lieferant:
SIA ENAMINE
Hersteller-Artikelnummer::
EN300105228.1G
Lokale Artikelnummer::
ENAMEN300105228.1G
Beschreibung:
2-Methyl-5-nitrobenzotrifluorid
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-15132R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15132R
Lokale Artikelnummer::
BOSSBS-15132R
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:
Bernd Kraft
Beschreibung:
Pyrogallol, reinst
Artikel-Nr:
(BOSSBS-9073R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9073R-CY3
Lokale Artikelnummer::
BOSSBS-9073R-CY3
Beschreibung:
C22orf31, also known as HS747E2A or bK747E2.1, is a 290 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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Nitrilotriessigsäure 99%
Artikel-Nr:
(APOSPC6688-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC6688-25G
Lokale Artikelnummer::
APOSPC6688-25G
Beschreibung:
Ethylioddifluoracetat 97%
VE:
1 * 25 g
Lieferant:
Thermo Scientific
Beschreibung:
Pivalinsäure 99%
Artikel-Nr:
(CHMPFL1087.POR)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
FL1087.POR
Lokale Artikelnummer::
CHMPFL1087.POR
Beschreibung:
2-Iod-1-phenylethan
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-9073R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9073R-A647
Lokale Artikelnummer::
BOSSBS-9073R-A647
Beschreibung:
C22orf31, also known as HS747E2A or bK747E2.1, is a 290 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-15134R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15134R-HRP
Lokale Artikelnummer::
BOSSBS-15134R-HRP
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. Translo-acations 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 C22orf26 gene product has been provisionally designated C22orf26 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15132R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15132R-A555
Lokale Artikelnummer::
BOSSBS-15132R-A555
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
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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