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Ethyl+3-(2-aminophenyl)acrylate
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Ethyl+3-(2-aminophenyl)acrylate
Artikel-Nr:
(94517-1ML)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
94517-1ML
Lokale Artikelnummer::
SUPL94517-1ML
Beschreibung:
Organic Standard, Quinoline, ≥98.0% (GC), 97.5 - 102.2 wt. % (NT)
VE:
1 * 1 mL
Lieferant:
Thermo Fisher Scientific
Beschreibung:
PETG, glasklar, mit HDPE-Schraubkappe und planem Boden.
Lieferant:
Thermo Fisher Scientific
Beschreibung:
PETG, transparent, mit HDPE-Schraubverschluss.
Artikel-Nr:
(BOSSBS-9372R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9372R-CY5
Lokale Artikelnummer::
BOSSBS-9372R-CY5
Beschreibung:
Protein geranylgeranyltransferase type I (GGTase-I) transfers a geranylgeranyl group to the cysteine residue of candidate proteins containing a C-terminal CAAX motif in which 'A' is an aliphatic amino acid and 'X' is leucine (summarized by Zhang et al., 1994 [PubMed 8106351]). The enzyme is composed of a 48-kD alpha subunit (FNTA; MIM 134635) and a 43-kD beta subunit, encoded by the PGGT1B gene. The FNTA gene encodes the alpha subunit for both GGTase-I and the related enzyme farnesyltransferase.[supplied by OMIM, Mar 2010]
VE:
1 * 100 µl
Lieferant:
ENTEGRIS
Beschreibung:
Conical pocket holds one wafer face down contacting only the edge of the wafer.
Lieferant:
Alfa Aesar
Beschreibung:
Silver, brazing alloy (Ag:Sn; 3.5:96.5 wt%), Ø 3.0 mm (0.13 in)
Artikel-Nr:
(BOSSBS-9369R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9369R-CY5.5
Lokale Artikelnummer::
BOSSBS-9369R-CY5.5
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-9369R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9369R-CY5
Lokale Artikelnummer::
BOSSBS-9369R-CY5
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
Lieferant:
Brand
Beschreibung:
Borosilikatglas 3.3, mit PP-Stopfen.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Acetamidoxime
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
N-Formylsaccharin
Artikel-Nr:
(BOSSBS-15131R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15131R-CY5
Lokale Artikelnummer::
BOSSBS-15131R-CY5
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-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15132R-CY3
Lokale Artikelnummer::
BOSSBS-15132R-CY3
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-9986R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9986R-A750
Lokale Artikelnummer::
BOSSBS-9986R-A750
Beschreibung:
C22orf36 is a 315 amino acid protein that contains two LRR (leucine-rich) repeats and exists as two alternatively spliced isoforms. C22orf36 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
Artikel-Nr:
(BLDPBD20315-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD20315-500G
Lokale Artikelnummer::
BLDPBD20315-500G
Beschreibung:
Cyclopentancarbonsäure 98%
VE:
1 * 500 g
Artikel-Nr:
(BOHLD647-24)
Lieferant:
Bohlender
Hersteller-Artikelnummer::
D647-24
Lokale Artikelnummer::
BOHLD647-24
Beschreibung:
Aus PA verstärkt mit Glasfaser zum Anziehen und Lösen von Schraubverbindungen auch bei hohen Arbeitstemperaturen.
VE:
1 * 1 ST
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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