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4-Oxohexahydrocyclopenta[c]pyrrole-2-carboxylic+acid+tert-butyl+e


6 037  results were found

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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
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

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

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

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15131R-A647
Lokale Artikelnummer:: BOSSBS-15131R-A647
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
Lieferant:  Alfa Aesar
Beschreibung:   Bis(2-chlorethyl)ether ≥99%
Artikel-Nr: (TSLA75056)

Lieferant:  TECHNICAL QUARTZ SOLUTIONS
Hersteller-Artikelnummer:: 75056
Lokale Artikelnummer:: TSLA75056
Beschreibung:   Quartz, transparent, glazed.
VE:  1 * 1 ST
Artikel-Nr: (BOSSBS-9440R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9440R-CY5
Lokale Artikelnummer:: BOSSBS-9440R-CY5
Beschreibung:   MTA1 is a component of the NURD (nucleosome remodeling and histone deacetylation) complex, which is associated with ATP-dependent chromatin-remodeling and histone deacetylase activity. MTA1 functions in conjunction with other components of NURD to mediate transcriptional repression as it facilitates the association of repressor molecules with the chromatin. Structurally, MTA1 contains a single SH3-binding motif and a zinc finger domain, along with a region similar to the co-repressor protein N-Cor. MTA1 is normally expressed at low levels in various tissues and is more highly expressed in testis. Overexpression of MTA1 correlates with tumor invasion and metastasis in various carcinomas including colorectal, gastrointestinal and breast carcinomas. Elevation of MTA1 levels in these tumors appears to enhance the metastases to lymph nodes, increase mammary cell motility and potentiate growth, and therefore may be an indicator for assessing the potential malignancies of various tumors. A similar protein, MTA2, also designated MTA1-L1 (MTA1-like protein 1), shares more than 55% sequence homology with MTA1 and is ubiquitously expressed.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-9440R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9440R
Lokale Artikelnummer:: BOSSBS-9440R
Beschreibung:   MTA1 is a component of the NURD (nucleosome remodeling and histone deacetylation) complex, which is associated with ATP-dependent chromatin-remodeling and histone deacetylase activity. MTA1 functions in conjunction with other components of NURD to mediate transcriptional repression as it facilitates the association of repressor molecules with the chromatin. Structurally, MTA1 contains a single SH3-binding motif and a zinc finger domain, along with a region similar to the co-repressor protein N-Cor. MTA1 is normally expressed at low levels in various tissues and is more highly expressed in testis. Overexpression of MTA1 correlates with tumor invasion and metastasis in various carcinomas including colorectal, gastrointestinal and breast carcinomas. Elevation of MTA1 levels in these tumors appears to enhance the metastases to lymph nodes, increase mammary cell motility and potentiate growth, and therefore may be an indicator for assessing the potential malignancies of various tumors. A similar protein, MTA2, also designated MTA1-L1 (MTA1-like protein 1), shares more than 55% sequence homology with MTA1 and is ubiquitously expressed.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9440R-A750
Lokale Artikelnummer:: BOSSBS-9440R-A750
Beschreibung:   MTA1 is a component of the NURD (nucleosome remodeling and histone deacetylation) complex, which is associated with ATP-dependent chromatin-remodeling and histone deacetylase activity. MTA1 functions in conjunction with other components of NURD to mediate transcriptional repression as it facilitates the association of repressor molecules with the chromatin. Structurally, MTA1 contains a single SH3-binding motif and a zinc finger domain, along with a region similar to the co-repressor protein N-Cor. MTA1 is normally expressed at low levels in various tissues and is more highly expressed in testis. Overexpression of MTA1 correlates with tumour invasion and metastasis in various carcinomas including colorectal, gastrointestinal and breast carcinomas. Elevation of MTA1 levels in these tumours appears to enhance the metastases to lymph nodes, increase mammary cell motility and potentiate growth, and therefore may be an indicator for assessing the potential malignancies of various tumours. A similar protein, MTA2, also designated MTA1-L1 (MTA1-like protein 1), shares more than 55% sequence homology with MTA1 and is ubiquitously expressed.
VE:  1 * 100 µl
Lieferant:  Sigma-Aldrich
Beschreibung:   Dimedon, Sigma-Aldrich®

Lieferant:  Merck
Hersteller-Artikelnummer:: 8.41034.0050
Lokale Artikelnummer:: MERC8.41034.0050
Beschreibung:   Aminoacetonitril-Sulfat zur Synthese, Sigma-Aldrich®
VE:  1 * 50 g
Artikel-Nr: (BLDPBD14303-10G)

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD14303-10G
Lokale Artikelnummer:: BLDPBD14303-10G
Beschreibung:   Bis(hexylene glycolato)diboron 98%
VE:  1 * 10 g
Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: L20016700IO
Lokale Artikelnummer:: EHERL20016700IO
Beschreibung:   Organic Standard, 2,3',4,4',5,5'-Hexachlorbiphenyl (PCB Nr. 167) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:  1 * 10 mL
Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: L20018900IO
Lokale Artikelnummer:: EHERL20018900IO
Beschreibung:   Organic Standard, 2,3,3',4,4',5,5'-Heptachlorbiphenyl (PCB Nr. 189) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:  1 * 10 mL
Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: L20020500IO
Lokale Artikelnummer:: EHERL20020500IO
Beschreibung:   Organic Standard, 2,3,3',4,4',5,5',6-Octachlorbiphenyl (PCB Nr. 205) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:  1 * 10 mL
Preis auf Anfrage
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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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