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Aurora Manufacturing Facility

Aurora Manufacturing Facility Our 65000 sq. ft. manufacturing facility in Aurora OH USA includes a 12000 sq. ft. excipient processing center 3000 sq. ft. for repackaging 35000 sq. ft. warehouse 8000 sq. ft. office 8000 sq. ft. manufacturing area a...

Back to Basics 2: Mobile Phase Selection In HPLC & UHPLC

Back to Basics 2: Mobile Phase Selection In HPLC & UHPLC Webinar Thursday 28th January 2021 15:00 to 16:00 CEST (Berlin Paris Madrid) Replay Mobile phase composition is a fundamental decision which has a major impact on the separation of analytes ...

HPLC

HPLC The right choice of chemical is crucial for your chromatography process. Below an overview of our chemical range for chromatography. Are you looking for columns instruments or other consumables as well? Akcie Chemické novinky Kontakt MSDS Cer...

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imagination at work Application note 29-0642-95 AA Chromatography systems Depletion of albumin from serum samples using ÄKTA™ start Albumin comprises 55% to 65% of the total protein in serum. The abundance of this protein makes it difficult to stu...

Liquid Chromatography - Sample Preparation

Liquid Chromatography - Sample Preparation Sample preparation is key but often overlooked step in the chromatography process. Every sample is unique and what works for one preparation may not work as well for another. That’s why Avantor offers a c...

Final fill for cell therapy

Final fill for cell therapy The cell therapy drug product is configured in different ways depending on the required delivery of the cells/tissues. For example delivery of chondrocytes for cartilage repair is administered by an injection. Expanded ...

Improve Your Biochromatography Separations - How to Optimize your Charge Variant Analysis

Improve Your Biochromatography Separations - How to Optimize your Charge Variant Analysis Webinar Thursday November 7th 2019 15:00 to 16:00 CEST (Berlin Paris Madrid) PRESENTED IN ENGLISH Replay Email Alerts Free Registration Chat Area Certificate...

CS-Vegetables-2019

CASE STUDY Vegetables FDA validated molecular method to detect C. cayetanensis in food samples Keyword: Cyclospora cayetanensis Fresh produce Prepared dish qPCR Aim of the study: Evaluate the performance of the FDA method for detection of C. Cayet...

Final fill for mAbs

Final fill for mAbs Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO Cla...

Stopová analýza a stanovení kovů

Stopová analýza a stanovení kovů Při analýze kovů se nyní shromažďují důkazy o prvcích z těch nejmenších stopových množství v rozsahu ppm ppb a ppt pomocí sofistikovaných nástrojů jako jsou AAS ICP-OES nebo v poslední době také ICP-MS. Více než po...

Upstream processing for vaccines

Upstream processing for vaccines Optimal production of vaccines is achieved in mammalian expression and insect systems using cell lines that are anchorage-dependent or suspension enabled. For most vaccines optimal production is achieved in mammali...

Spektrofotometre

Spektrofotometre Spektrofotometre majú široké využitie vo viacerých laboratóriách so zameraním na výskum kontrolu kvality a farmaceutiku a uplatňujú sa v oblasti chémie biochémie prírodných vied analýzy vody a v potravinárskom a nápojovom priemysl...

Downstream purification for recombinant proteins

Downstream purification for recombinant proteins With more than 30 years of chromatography experience developed products and services we have every solution to meet your needs. Our J.T.Baker® brand BAKERBOND™ chromatography resins have been used s...

Upstream processing for microbial-based recombinant proteins

Upstream processing for microbial-based recombinant proteins Using microbial fermentation for the development and manufacture of recombinant proteins keeps on showing advantages e.g for the expression of proteins that do not require post-translati...

Final fill for vaccines

Final fill for vaccines Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO...

Upstream processing for cell therapy

Upstream processing for cell therapy Compared to production volumes associated with other biologics (e.g. mAbs: 2000L to 10000L) cell therapy production volumes are more commonly between 1L to 10L. Even the quality parameters are different. Instea...