2,2-Dimethylbut-3-ynoic+acid
Artikel-Nr:
(80013.)
Lieferant:
Biotium
Hersteller-Artikelnummer::
80013
Lokale Artikelnummer::
BTIU80013
Beschreibung:
Calcein
VE:
1 * 100 mg
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:
APOLLO SCIENTIFIC
Beschreibung:
Mono(boc)(PEO)-3-diamine, boc-DOOA 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:
VWR Chemicals
Beschreibung:
EDTA Tetranatriumsalz Hydrat ≥99,5%, Ultrareine Qualität
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
Lieferant:
Alfa Aesar
Beschreibung:
2-Cyano-2-Methylpropionsäure Ethylester 97%
Lieferant:
Merck
Beschreibung:
Xylenolorange Tetranatriumsalz, Supelco®
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:
Thermo Scientific
Beschreibung:
Anilinblau, wasserlöslich
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
Artikel-Nr:
(BOSSBS-8079R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8079R-A350
Lokale Artikelnummer::
BOSSBS-8079R-A350
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)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8079R
Lokale Artikelnummer::
BOSSBS-8079R
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-15140R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15140R-CY7
Lokale Artikelnummer::
BOSSBS-15140R-CY7
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
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