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Hai cercato: Pompe+a+tamburo


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Codice catalogo: (224-2061)
Fornitore: Saint Gobain Life Sciences
Codice articolo fornitore: R6002-23
Codice articolo locale: VERNR6002-23
Descrizione: TUBO PER POMPE, NORPRENE, TIPO B 1,6X1,6 1 * 15 m
UOM: 1 * 15 m


Fornitore: VACUUBRAND
Descrizione: Per collegare le pompe con i tubi di vuoto.
Alluminio.

Codice catalogo: (613-0120)
Fornitore: B. Braun
Codice articolo fornitore: 8728844F
Codice articolo locale: BRAU8728844F
Descrizione: PP syringe with safe plunger backstop and minimal residual volume.
UOM: 1 * 100 pezzi

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Codice catalogo: (224-2065)
Fornitore: Saint Gobain Life Sciences
Codice articolo fornitore: AFL00022-S
Codice articolo locale: VERNAFL00022-S
Descrizione: TUBO PER POMPE, NORPRENE TIPO F 8,0X1,6 1 * 15 m
UOM: 1 * 15 m


Codice catalogo: (BOSSBS-13254R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-A750
Codice articolo locale: BOSSBS-13254R-A750
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-A555
Codice articolo locale: BOSSBS-13254R-A555
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-A647
Codice articolo locale: BOSSBS-13254R-A647
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-HRP
Codice articolo locale: BOSSBS-13254R-HRP
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-A680
Codice articolo locale: BOSSBS-13254R-A680
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-A350
Codice articolo locale: BOSSBS-13254R-A350
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R
Codice articolo locale: BOSSBS-13254R
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-FITC
Codice articolo locale: BOSSBS-13254R-FITC
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-A488
Codice articolo locale: BOSSBS-13254R-A488
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-CY3
Codice articolo locale: BOSSBS-13254R-CY3
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-CY5
Codice articolo locale: BOSSBS-13254R-CY5
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13254R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-13254R-CY7
Codice articolo locale: BOSSBS-13254R-CY7
Descrizione: This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
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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