180009 Results for: "Batch Pressure Filter Cloth"

Supplier: VICI JOUR RESEARCH

The stainless steel in-line filter has virtually no dead volume and can be used in various applications without significant band broadening or loss of efficiency. This version is intended for analytical use between the autosampler injection valve and the column.

Supplier: VWR Collection

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

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: 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: 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.

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: EPPENDORF

Combitips advanced® function according to the positive displacement principle, as a result they always dispense the correct volume independently of the density of the liquid and its flow characteristics (e.g., increased vapour pressure or increased viscosity). They are ideal for use with all Eppendorf multipettes.

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: Avantor

J.T.Baker® Viral Inactivation Solution Ultrapure bioreagent is a highly effective, ready-to-use product, specifically developed for detergent-based viral inactivation in biopharmaceutical operations and plasma derived therapy processes. J.T.Baker® Viral Inactivation Solution is formulated with non-ionic detergent, that is readily biodegradable and alkylphenol ethoxylate free, addressing environmental concerns associated with REACH. This innovative solution is optimized to have low protein reactive impurities, low viscosity and compatibility with typical downstream processes. J.T.Baker® Viral Inactivation Solution Ultrapure bioreagent is available in a variety of sizes to support development to large scale commercial batches. Detail description provided in technical literature.

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.