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2,2-Dimethylbut-3-ynoic+acid
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2,2-Dimethylbut-3-ynoic+acid
Artikel-Nr:
(BOSSBS-9073R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9073R
Lokale Artikelnummer::
BOSSBS-9073R
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:
Alfa Aesar
Beschreibung:
2-Cyano-2-Methylpropionsäure Ethylester 97%
Artikel-Nr:
(ROCK100-601-143)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
100-601-143
Lokale Artikelnummer::
ROCK100-601-143
Beschreibung:
This product has been assayed against 1.0 µg of D-Amino Acid Oxidase (Pig Kidney) in a standard ELISA using Peroxidase conjugated Affinity Purified anti-Sheep IgG (H&L) (Goat) and ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid))
VE:
1 * 2 mL
Lieferant:
Thermo Scientific
Beschreibung:
Anilinblau, wasserlöslich
Artikel-Nr:
(APOSOR3597-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR3597-1G
Lokale Artikelnummer::
APOSOR3597-1G
Beschreibung:
1-Boc-6-chlor-2-indolboronsäure 98%
VE:
1 * 1 g
Lieferant:
Alfa Aesar
Beschreibung:
trans-4-Hydroxy-D-proline 97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Mono(boc)(PEO)-3-diamine, boc-DOOA 98%
Artikel-Nr:
(430841000.)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
430841000
Lokale Artikelnummer::
ACRO430841000
Beschreibung:
Methylchlorformiat 99%, AcroSeal®
VE:
1 * 100 mL
Artikel-Nr:
(BOSSBS-8112R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8112R-FITC
Lokale Artikelnummer::
BOSSBS-8112R-FITC
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:
Thermo Scientific
Beschreibung:
trans-1,2-Diaminocyclohexan-N,N,N',N'-tetraessigsäure Monohydrat 98%
Artikel-Nr:
(BOSSBS-8079R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8079R-A750
Lokale Artikelnummer::
BOSSBS-8079R-A750
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:
Merck
Beschreibung:
Xylenolorange Tetranatriumsalz, Supelco®
Artikel-Nr:
(BOSSBS-15140R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15140R-A750
Lokale Artikelnummer::
BOSSBS-15140R-A750
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-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8079R-HRP
Lokale Artikelnummer::
BOSSBS-8079R-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. 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-8079R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8079R-CY5.5
Lokale Artikelnummer::
BOSSBS-8079R-CY5.5
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
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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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