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ELBE WERKSTATTEN
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
N-Ethyl-5-fluoro-2-nitroaniline 97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ethyl-1,3-benzothiazol-2-carboxylat
Lieferant:
Merck
Beschreibung:
N-Methylmorpholin-N-oxid 50% in wässriger Lösung, Sigma-Aldrich®
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ethyl-2,6-dichloropyridine-3-carboxylate
Artikel-Nr:
(BLDPBD33651-100G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD33651-100G
Lokale Artikelnummer::
BLDPBD33651-100G
Beschreibung:
Ethyl-1-aminocyclopropancarboxylathydrochlorid 95%
VE:
1 * 100 g
Lieferant:
Alfa Aesar
Beschreibung:
2-Propylvaleriansäure ≥98%
Artikel-Nr:
(71747-50MG)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
71747-50MG
Lokale Artikelnummer::
SUPL71747-50MG
Beschreibung:
Sodium ionophore X is generally used in the preparation of ion-selective electrode (ISE).
VE:
1 * 50 mg
Lieferant:
Alfa Aesar
Beschreibung:
Ethyl-4-hydroxy-3-nitrobenzoate 98%
Artikel-Nr:
(BOSSBS-9369R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9369R-CY3
Lokale Artikelnummer::
BOSSBS-9369R-CY3
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
Artikel-Nr:
(BOSSBS-15134R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15134R
Lokale Artikelnummer::
BOSSBS-15134R
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-9485R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9485R-FITC
Lokale Artikelnummer::
BOSSBS-9485R-FITC
Beschreibung:
The ENTHD1 gene is conserved in chimpanzee, dog, cow, mouse and rat, and maps to human chromosome 22q13.1. 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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15134R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15134R-A680
Lokale Artikelnummer::
BOSSBS-15134R-A680
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-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
Artikel-Nr:
(BOSSBS-9485R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9485R-CY7
Lokale Artikelnummer::
BOSSBS-9485R-CY7
Beschreibung:
The ENTHD1 gene is conserved in chimpanzee, dog, cow, mouse and rat, and maps to human chromosome 22q13.1. 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.
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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