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Benzoic+acid-acyl-\\\\u03B2-D-glucuronide
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Benzoic+acid-acyl-\\\\u03B2-D-glucuronide
Artikel-Nr:
(RTC000068-1L)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
RTC000068-1L
Lokale Artikelnummer::
SUPLRTC000068-1L
Beschreibung:
Natriumazid 0,05% in Wasser, Supelco®
VE:
1 * 1 L
Artikel-Nr:
(APOSOR930972-500G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR930972-500G
Lokale Artikelnummer::
APOSOR930972-500G
Beschreibung:
m-Tolyldiethanolamine 98%
VE:
1 * 500 g
Lieferant:
Alfa Aesar
Beschreibung:
(S)-(-)-1,1'-Bi-2-naphthol ≥99%
Lieferant:
Alfa Aesar
Beschreibung:
Bis(2-benzamidophenyl)disulphide 97%
Lieferant:
SIGMA ALDRICH MICROSCOPY
Beschreibung:
Nitro Blue Tetrazolium is a tetrazole compound with two tetrazole rings.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Dimesna
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:
Thermo Scientific
Beschreibung:
(±)-Camphen 75% remainder mainly alpha-fenchene
Lieferant:
Alfa Aesar
Beschreibung:
Pivalaldehyd (Trimethylacetaldehyd) 95%
Lieferant:
Alfa Aesar
Beschreibung:
Hydroxypivalic acid ≥97%
Lieferant:
BIOMOL RESEARCH LABORATORIES
Beschreibung:
BIS-TRIS-Propan
Artikel-Nr:
(BOSSBS-15134R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15134R-FITC
Lokale Artikelnummer::
BOSSBS-15134R-FITC
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-15131R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15131R-FITC
Lokale Artikelnummer::
BOSSBS-15131R-FITC
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 C22orf13 gene product has been provisionally designated C22orf13 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15132R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15132R-A350
Lokale Artikelnummer::
BOSSBS-15132R-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. The C22orf15 gene product has been provisionally designated C22orf15 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15131R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15131R-HRP
Lokale Artikelnummer::
BOSSBS-15131R-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. The C22orf13 gene product has been provisionally designated C22orf13 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9485R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9485R-A555
Lokale Artikelnummer::
BOSSBS-9485R-A555
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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