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Hai cercato: 3\\\'-Bromo-2,2\\\':5\\\',2\\\'\\\'-terthiophene


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Fornitore: TCI EUROPE
Descrizione: 3'-Bromo-2,2':5',2''-terthiophene ≥97.0% (by GC)

Fornitore: TCI EUROPE
Descrizione: 5''-Bromo-2,2':5',2''-terthiophene-5-carboxaldehyde ≥94.0% (by GC)

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Fornitore: TCI EUROPE
Descrizione: 5,5''-Dibromo-2,2':5',2''-terthiophene ≥97.0% (by GC)

Fornitore: Apollo Scientific
Descrizione: 2,2':5',2''-Terthiophene 98%

Fornitore: Apollo Scientific
Descrizione: 2,2':5',2''-Terthiophene-5-carboxaldehyde

Codice catalogo: (TCIAT1805-1G)
Fornitore: TCI EUROPE
Codice articolo fornitore: T1805-1G
Codice articolo locale: TCIAT1805-1G
Descrizione: 2,2':5',2''-Terthiophene-5-carboxaldehyde ≥98.0% (by HPLC)
UOM: 1 * 1 g


Fornitore: Thermo Scientific
Descrizione: 2,2':5',2''-Terthiophene ≥99%
Fornitore: TCI EUROPE
Descrizione: 2,2':5',2''-Terthiophene ≥98.0% (by GC), purified by sublimation

Codice catalogo: (TCIAT2639-1G)
Fornitore: TCI EUROPE
Codice articolo fornitore: T2639-1G
Codice articolo locale: TCIAT2639-1G
Descrizione: 2,2':5',2''-Terthiophene-5,5''-dicarboxaldehyde ≥98.0% (by GC)
UOM: 1 * 1 g


Fornitore: TCI EUROPE
Descrizione: 5,5''-Bis(trimethylstannyl)-2,2':5',2''-terthiophene ≥98.0% (by HPLC)

Fornitore: Thermo Scientific
Descrizione: 2,3':4',2''-Terthiophene 95%

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Codice catalogo: (BOSSBS-9990R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-9990R-A680
Codice articolo locale: BOSSBS-9990R-A680
Descrizione: Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin-1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterised by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt's lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11722R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-11722R-A750
Codice articolo locale: BOSSBS-11722R-A750
Descrizione: Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin 1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterised by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11722R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-11722R-CY5
Codice articolo locale: BOSSBS-11722R-CY5
Descrizione: Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin ?1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterized by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt抯 lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11722R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-11722R-A555
Codice articolo locale: BOSSBS-11722R-A555
Descrizione: Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin ?1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterized by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt抯 lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11722R)
Fornitore: Bioss
Codice articolo fornitore: BS-11722R
Codice articolo locale: BOSSBS-11722R
Descrizione: Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin ?1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterized by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt抯 lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
UOM: 1 * 100 µl


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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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