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Producent: Avantor Fluid Handling
Opis: Complete pump systems for accurate fluid delivery - with an intuitive touch-screen interface.

MasterflexLive® 2 year warranty

Producent: Avantor Fluid Handling
Opis: Get the most our of your Masterflex® I/P® Easy-Load® Pump Head with these replacement parts.

Numer katalogowy: (181-0589)
Producent: Sartorius
Opis: The Microsart® e.jet is a laboratory vacuum pump which creates vacuum and concomitantly transfers the filtered liquid to waste.
j.m.: 1 * 1 SZT


Numer katalogowy: (516-0952)
Producent: Cytiva (Formerly Pall Lab)
Opis: The Sentino® pump system is ideal for microbiological MF technique using Pall MicroFunnel™ filtration units. Designed to use peristaltic action to draw the sample through the filter and send filtrate directly to drain or waste collection. The housing is a PC ABS-blended polymer, the keypad and label PE, the pump head PEI with PTFE-filled PBT rollers. The fluid path adapter is PP.
j.m.: 1 * 1 SZT


Numer katalogowy: (BOSSBS-13254R-A680)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-13254R-CY3)
Producent: Bioss
Opis: 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].
j.m.: 1 * 100 µl


Numer katalogowy: (MFLX75800-62)
Producent: Avantor Fluid Handling
Opis: Multiple designs—either dry pump cavity or lubricant filled—to best fit your system requirements.
j.m.: 1 * 1 SZT

1 year warranty


Producent: Avantor Fluid Handling
Opis: Long pumping life with superior flexibility reduces downtime and tubing failure.
Producent: Avantor Fluid Handling
Opis: Make the most of your Masterflex drives replacement parts and service kits.

Numer katalogowy: (MFLX07559-04)
Producent: Avantor Fluid Handling
Opis: Optimize performance of your Masterflex modular drives.
j.m.: 1 * 1 SZT


Producent: Avantor Fluid Handling
Opis: Maintain flexibility at extreme temperatures.
Producent: Avantor Fluid Handling
Opis: Compatible with aggressive chemicals.
Numer katalogowy: (BOSSBS-13254R-CY7)
Producent: Bioss
Opis: 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].
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-13254R-CY5)
Producent: Bioss
Opis: 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].
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-13254R-FITC)
Producent: Bioss
Opis: 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].
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-13254R-A488)
Producent: Bioss
Opis: 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].
j.m.: 1 * 100 µl


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Zapasy tego artykułu są ograniczone, ale możliwe, że jest on dostępny w pobliskim magazynie. Upewnij się, że jesteś zalogowany na stronie, aby móc sprawdzić dostępność zapasów. Jeśli call ciągle się wyświetla i potrzebujesz pomocy, zadzwoń na 58 323 82 00.
Ten produkt jest ograniczony w dostępie i można go zamówić tylko przy użyciu zaaprobowanego konta. Jeśli potrzebujesz pomocy, napisz do Działu Prawnego VWR na tomasz.chrobak@pl.vwr.com
Do zakupu tego produktu może być potrzebna dodatkowa dokumentacja. Przedstawiciel VWR skontaktuje się z Tobą w razie potrzeby.
Ten produkt jest zablokowany na stronie internetowej. W celu zamówienia, skontaktuj się z Działem Obsługi Klienta.
Produkt oryginalny został wycofany. Dostępny jest wskazny zamiennik .
Wybrany produkt został wycofany - sprzedaż do wyczerpania zapasów. Dostępne zamienniki można znaleźć poprzez wpisanie powyższego numeru katalogowego VWR w okno wyszukiwarki. Jeśli potrzebujesz dalszej pomocy, prosimy o kontakt z Działem Doradztwa Produktowego pod numerem telefonu 58 3238 220.
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