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2,2-Dimethylbut-3-ynoic+acid
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2,2-Dimethylbut-3-ynoic+acid
Lieferant:
Alfa Aesar
Beschreibung:
Stabilized with potassium carbonate
Lieferant:
Sigma-Aldrich
Beschreibung:
2,2-Dimethylpentan, Sigma-Aldrich®
Lieferant:
Thermo Scientific
Beschreibung:
Bromkresolgrün Natriumsalz, wasserlöslich Indikator
Lieferant:
Alfa Aesar
Beschreibung:
Silber ≥99,99% (Metall-Basis), Schnecke, Länge 12.7 mm (0.50 in), Ø 6.35 mm (0.25 in)
Artikel-Nr:
(MODU395413)
Lieferant:
Vitrex Medical A/S
Hersteller-Artikelnummer::
395413
Lokale Artikelnummer::
MODU395413
Beschreibung:
Sterile safety lancets intended for blood glucose and other <i>in vitro</i> diagnostic tests. Protects the health workers facing accidental needle-stick injury while caring for patients, putting themselves at risk to bloodborne illnesses including the AIDS virus and Hepatitis.
VE:
1 * 100 ST
Artikel-Nr:
(BOSSBS-5592R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5592R-FITC
Lokale Artikelnummer::
BOSSBS-5592R-FITC
Beschreibung:
This gene is the cellular homolog of the Yamaguchi sarcoma virus oncogene. The encoded protein has tyrosine kinase activity and belongs to the src family of proteins. This gene lies in close proximity to thymidylate synthase gene on chromosome 18, and a corresponding pseudogene has been found on chromosome 22. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5592R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5592R-A555
Lokale Artikelnummer::
BOSSBS-5592R-A555
Beschreibung:
This gene is the cellular homolog of the Yamaguchi sarcoma virus oncogene. The encoded protein has tyrosine kinase activity and belongs to the src family of proteins. This gene lies in close proximity to thymidylate synthase gene on chromosome 18, and a corresponding pseudogene has been found on chromosome 22. [provided by RefSeq].
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Silber ≥99,99% (Metall-Basis), Schnecke, Länge 6.35 mm (0.25 in), Ø 3.175 mm (0.125 in)
Lieferant:
Alfa Aesar
Beschreibung:
Silber hart ≥99,998% (Metall-Basis), Folie, Premion®, hart, Dicke 0.25 mm (0.01 in)
Artikel-Nr:
(BOSSBS-9990R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9990R-A750
Lokale Artikelnummer::
BOSSBS-9990R-A750
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11722R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11722R-A647
Lokale Artikelnummer::
BOSSBS-11722R-A647
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(41264.KS)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
41264.KS
Lokale Artikelnummer::
ALFA41264.KS
Beschreibung:
Silber ≥99,99% (Metall-Basis), Aufdampfplatte, Ø 50.8 mm (2.0 in), Dicke 3.18 mm (0.125 in)
VE:
1 * 1 ST
Lieferant:
Sigma-Aldrich
Beschreibung:
2,2'-Dipyridyldisulfid, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-9990R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9990R-A680
Lokale Artikelnummer::
BOSSBS-9990R-A680
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11722R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11722R-A750
Lokale Artikelnummer::
BOSSBS-11722R-A750
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11722R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11722R-CY5
Lokale Artikelnummer::
BOSSBS-11722R-CY5
Beschreibung:
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.
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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