2-(4-Pyridinyloxy)-ethanamine+hydrochloride
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Bromo(difluoro)acetic anhydride
Lieferant:
Alfa Aesar
Beschreibung:
(±)-1,1′-Bi-2-naphthol ≥99%
Artikel-Nr:
(BOSSBS-9987R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9987R-A750
Lokale Artikelnummer::
BOSSBS-9987R-A750
Beschreibung:
C22orf9 is a 404 amino acid protein that exists as three alternatively spliced isoforms and 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
Lieferant:
Alfa Aesar
Beschreibung:
Ninhydrin ≥99%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Mycophenolic acid-O-β-D-glucuronide ≥97%
Lieferant:
Thermo Scientific
Beschreibung:
1-Methyl-1H-pyrazol-4-boronsäurepinakolester 97+%
Artikel-Nr:
(BOSSBS-15140R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15140R-A647
Lokale Artikelnummer::
BOSSBS-15140R-A647
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:
(J65402.03)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
J65402.03
Lokale Artikelnummer::
ALFAJ65402.03
Beschreibung:
N6-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-fluoro-2'-deoxyadenosine 98%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-15125R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15125R-A680
Lokale Artikelnummer::
BOSSBS-15125R-A680
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-15140R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15140R
Lokale Artikelnummer::
BOSSBS-15140R
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-8079R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8079R-CY7
Lokale Artikelnummer::
BOSSBS-8079R-CY7
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Dichloroacetaldehyde hydrate 90%
Lieferant:
Alfa Aesar
Beschreibung:
Pivalamidine hydrochloride 98%
Artikel-Nr:
(APOSOR6496-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR6496-5G
Lokale Artikelnummer::
APOSOR6496-5G
Beschreibung:
Aminoacetaldehyddiethylacetal
VE:
1 * 5 g
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
Iminodiessigsäure 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-(Pentafluoropropenyl)pivalate 98%
Preis auf Anfrage
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