Then after transfer coomassie stain the transferred gel and ponceau stain the membrane. Transfer one but coomassie stain the other. One thing you can do to see the effectiveness of the transfer is to run two replica gels. Larger proteins can take longer to transfer, so whatever is happening in your situation your transfer is not very effective. I think the issue is that your transfer is not effective. These are things you can do for the time being. We also put an ice pack into the bio-rad wet transfer. We usually make a 10x stock (without methanol) and immediately prior to running the transfer we make up 1L of 1x transfer buffer by adding 700mL water + 100mL 10x buffer + 200mL methanol. Make sure you are making the towbin transfer buffer properly - just prepare a fresh batch or buy it. That usually has worked for every protein I have tried to transfer/blot. There are aggregates in the HRP conjugated secondary antibody.įilter the secondary antibody agent and remove the aggregates.I use a 0.45 micron nitrocellulose membrane and do a wet transfer with bio-rad with CONSTANT amperage 400 milliamps for 75 minutes. The antibody reacts with the blocking solution. The blocking agent was not well dissolved. Keep shaking when incubating the antibody. Reduce the voltage to slow down the migrationĭecrease the secondary antibody concentrationĪir bubbles were trapped against the membrane during transferring or the antibody is not well distributed during incubation Migration was too fast during electrophoresis Substrate is not well-distributed during incubation Remove bubbles in the gap of gel and membrane when preparing for transferring. Modification of proteins, such as glycosylation or phosphorylation, can result in an increase of molecular weight of protein.Īir bubbles were trapped in the gap of gel and membrane during transferring. Increase a process or intensity of protein denaturation Run a secondary antibody control or choose other secondary antibody Non-specific signal caused by the secondary antibody The size of every isoform protein is different. Some proteins derived from the same gene have different isoforms. Use primary cells or less passaging cells to run a controlĭecrease the concentration of the primary or secondary antibodyĬhoose monoclonal antibody or affinity purified antibody to ensure antibody specificityĮxistence of the different protein isoforms Use fresh samples and use protein inhibitorĬells were cultured too many passages to result in protein variation Setting loading control can validate the secondary detecting system.Īvoid sodium azide in all solutions and containersĭirectly mix enzyme and substrate. Primary antibody and species, primary antibody and secondary antibody, or enzyme and substrate are not compatible. The reagents are not compatible with each other Increase the concentration of the antibody and the incubation time. Insufficient reaction of antibody to membrane Use effective antibody in expiration, avoid freezing- thawing repeatedly, and use fresh solution. Lower the concentration of your blocking solution and shorten blocking time. As a result, choose suitable methanol concentration according to different molecular weight. At the same time, it may cause shrinking or hardening of the gel to inhibit transferring of high molecular weight proteins. ![]() Too high concentration of methanol may result in the separation of protein and SDS and thus cause protein precipitation in the gel. Control transfer temperature and optimize transfer electricity and time. Always ensure assembling electrode correctly. Make sure there are no air bubbles between the gel and membrane during transfer. Use 0.2 µm size membrane for proteins smaller than 22 KD. Use 0.45um size membrane for proteins larger than 22KD. If the level of target protein in samples is low, try to increase amount of loading sample.Ĭhoose suitable pore size membrane. No or low level of target protein in samples Optimize blocking solution, decrease blocking time or decrease the concentration of proteins in the blocking solution. The antigen is blocked by blocking buffer Add Tween-20 to the washing buffer to reduce cross reaction. The antibody concentration may be too highĭecrease the concentration of primary antibody or secondary antibodyĬross-reaction between antibody and blocking agentĬhoose blocking solution without cross-reaction. Increase washing time and washing buffer’s volume Incubate in sufficient reaction solution to prevent the membrane from drying out. Use clean tweezer and operate with gloves to prevent membrane fouling.
0 Comments
Leave a Reply. |
Details
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |