183132 Results for: "Batch Pressure Filter Cloth"

Supplier: Brand

AR-Glas®.

Supplier: Brand

Borosilicate glass 3.3, with PP stopper.

Supplier: VWR Chemicals

SeraFree cryopreservation media is ready to use freezing media for cryopreservation of adherent or suspension cultured cells. The animal-free media composition eliminates batch-to-batch variability and is optimised for cell viability and cell growth after thawing. Suitable for use in environments that prohibit the use of animal-derived products.

Supplier: BIOCONCEPT

SF-4 baculovirus expression medium allows high yield expression of proteins well above all other commercially available media. The products has no variability therefore does not require initial batch testing and batch reservation.

Supplier: EPPENDORF

Combitips advanced® fungerar enligt principen om positiv förskjutning. Därför dispenserar de alltid rätt volym, oberoende av densiteten hos vätskan och dess flödeskarakteristika (t.ex. ökat ångtryck eller ökad viskositet). Idealiska för användning med alla Eppendorf multipetter.

Supplier: asecos

Recirculating air filter system UFA.20.30
Avoid complex wall, ceiling and roof penetrations and costly extract systems. Safe capturing of escaping vapours at the point where they are released or produced.
High flexibility in choosing the installation location
Active personal protection through safe capture of harmful vapours with retention in the filter system
Very low noise, ~39 dB(A)
ATEX complient: CE II 3/-G Ex ic nA IIB T4 Gc
Housing made of sheet-steel plastic laminated
With multistage filter system and power cord
Incl. VDE tested extraction and filter monitoring
Optical and acoustical alarm including potential-free alarm contact
Dimensions W×D×H: 305×555×210 mm
The plug-in recirculating air filter system UFA.20.30 is capable of retaining solvent vapours (hydrocarbons) permanently up to a filter saturation of more than 99,999%, under normal operating conditions as well as for a simulated accident in the safety storage cabinet.
A special version of the recirculating air filter system UFA.20.30-AUS is also available to meet the pressure conditions and volumetric flows of safety storage cabinets with a small internal volume. It can be installed on a wall bracket or in a convenient housing unit.

Supplier: QSONICA LLC

Flocell provides inline or continuous, large volume, batch sample processing. Flocell is ideal for mixing and dispersing applications.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: VWR Collection

This bag rack is used for batch preparation of samples prior to blending as well as sample storage after blending.

Supplier: VWR Chemicals

Avantor offers a wide range of REDOX (ORP) standards, which are produced from high quality reagents.These reference materials can be used as control standards to check the functionality of both the elextrodes and the measuring instruments. The values are temperature dependent, so it is important to control the environment of the measurement. A table of temperatue and corresponding Redox value is available on both the label and the batch specific certificate.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.

Supplier: USP

Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.