Lonza | FAQ DB http://www.lonzabio.com/meta/faq/ Thu, 17 May 2012 19:06:07 +0100 FeedCreator 1.7.2 http://www.lonzabio.com/fileadmin/images/lonza_logo_220_75.gif Lonza Cologne AG http://www.lonzabio.com/meta/faq/ Lonza Cologne AG Do I need a special media or protocol for culturing these diseased cells? http://www.lonzabio.com/go/faq/627 Lonza Cologne AG Do we know the severity of the asthma or the genotype of the cystic fibrosis donors? http://www.lonzabio.com/go/faq/626 Lonza Cologne AG How many passages can I use the diseased cells? http://www.lonzabio.com/go/faq/625 Lonza Cologne AG Do we have any Diseased Human Bronchial/Tracheal Epithelial Cells (DHBE) screened for Air Liquid Interface (ALI) differentiation using B-ALI? http://www.lonzabio.com/go/faq/624 Lonza Cologne AG Is the viability of cells from diseased or diabetic donors less than cells from normal donors? http://www.lonzabio.com/go/faq/623 Lonza Cologne AG Does the recommended media for each of the diabetic cells contain glucose? Is there a glucose-free media option? http://www.lonzabio.com/go/faq/622 Lonza Cologne AG Can cells from diseased or diabetic donors be shipped out of the U.S.? http://www.lonzabio.com/go/faq/621 Lonza Cologne AG Can you use the AdipoRed Assay on cells other than preadipocytes? http://www.lonzabio.com/go/faq/620 Lonza Cologne AG Can ProSieve EX running and transfer buffers be re-used? http://www.lonzabio.com/go/faq/615 Lonza Cologne AG I transfected neurons using the Y unit. After Nucleofection, there were precipitates in my culture. What can I do? http://www.lonzabio.com/go/faq/613 Lonza Cologne AG The basic protocol for adherent Nucleofection of neurons using the Y unit recommends to plate 150,000 freshly isolated or 300,000 cryopreserved ... http://www.lonzabio.com/go/faq/611 Lonza Cologne AG I would like to use the dipping electrode array for less than 24 wells. How can I keep non-required dipping electrodes clean? http://www.lonzabio.com/go/faq/608 Lonza Cologne AG I transfected neurons using the 4D-Nucleofector™ Y unit. During analysis I observed areas with low or no cell density, even in my no pulse ... http://www.lonzabio.com/go/faq/606 Lonza Cologne AG How can I find out if other 24-well culture plates than Greiner or Nunc are compatible to the dipping electrode array for adherent Nucleofection? http://www.lonzabio.com/go/faq/602 Lonza Cologne AG How can I best clean used dipping electrodes and store unused for later use? Can I wash used dipping electrodes in an ethanol bath? http://www.lonzabio.com/go/faq/601 Lonza Cologne AG How can I check the configuration or the warranty status of the laptop model which is delivered with the 96-well Shuttle System™? http://www.lonzabio.com/go/faq/596 Lonza Cologne AG How many culture/trans-wells does your B-ALI™ Media Kit kit provide? http://www.lonzabio.com/go/faq/592 Lonza Cologne AG What passage are your B-ALI™ cells when plating on transwells? http://www.lonzabio.com/go/faq/591 Lonza Cologne AG Won\'t the apical surface of B-ALI™ cells dry out in Air-Lifted culture? http://www.lonzabio.com/go/faq/590 Lonza Cologne AG How is the B-ALI™ media system performance tested? http://www.lonzabio.com/go/faq/589 Lonza Cologne AG