Search results for " protein L"
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				Real-Time Characterization of Biotherapeutics and Comparability of Biosimilars
								Real-Time Characterization of Biotherapeutics and Comparability of Biosimilars
	A major advantage of SPR-based analysis is its ability to estimate the association and dissociation rate constants, an …								
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				Managing Residual Impurities During Downstream Processing
								
	Increased understanding of potential impurities has spurred efforts to standardize monitoring procedures.
	By Cynthia A. Challener
	Manufacture of protein and other biologic drug substances via …								
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				Q&As with Industry Leaders
								
	
		Discovering the unknown: How does in silico process development change PD scientists’ work? 
		
	
	
		Jeanne Linke Northrop, BioPharm International 
		
		Nora Ketterer, Manager, Modeling Services…								
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				The Development and Application of a Monoclonal Antibody Purification Platform
								A purification scheme to maximize the efficiency of the purification process and product purity while minimizing the development time for early-phase therapeutic antibodies.
	
	
	
	The following ar…								
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				Milestones and Moderate Progress in 2012 Drug Approvals
								
	 
	
	   
First gene therapy and plant-based expression vector products approved in 2012. 
	
	In terms of product approvals, the past year can be considered reasonably successful. Twelve biopharm…								
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				Top Tips for Successful Development of Antibody Chromatography Processes
								But working with protein L, that only binds kappa subclass one, three and four, for instance, MabSelect™ VL, you could get a really high purity sample during the capture step. Since the lambda heterod…								
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				Optimizing your Cell Culture Process to Improve Productivity
								
	
		Cell Culture Process 
	
	
	
	In this video, Mary Szorik and Alicia Elwood at Cytiva, discuss the rationale for cell culture and analytical testing as well as the types of tests that can lead …								
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				Analytical Considerations for Successful Upstream Process Development with Spivey and Lane
								
	Spivey and Lane 
	
	Click here to view more Q&As >> 
	
	  
	
	  
	Analytic considerations for upstream processing – covering Process Analytic Technology (PAT), time-savings versus off-line ana…								
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				Tips for Purifying and Analyzing Cryo-EM Samples
								
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	Cryogenic electron microscopy (cryo-EM) provides possibilities to determine structures for more challenging proteins, such as membrane proteins and larger protein compl…								
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				Getting a Handle on Biopharma’s Most Critical Quality Attributes and Quality Control
								
	While the multiple attributes method gains ground and traditional lab methods improve, broad efforts are underway to determine biopharmaceuticals’ most significant critical quality attributes and en…