If your product does not perform as described on this datasheet, we will refund or replace your product...
Read our guarantee »This product is covered by the Abpromise guarantee. Our scientific support team are available to answer any questions or queries - fill out an inquiry form for ab59680 for help.
Alternatively, you can search the previous enquiries about this product to see if your query has already been answered.
|
|||||||||
|
|||||||||
The answer I received is still not specific enough. I wanted to know if it was based on a Tris Glycine gel or some other type of SDS-Page gel type. |
|||||||||
ANSWER: |
Thank you for your enquiry. I have recontacted the originator for detail information and they have confirmed that a Tris Glycine gel was used in the WB. If there is anything else that I can help you with, please do not hesitate to contact us. Have a nice day. |
||||||||
|
|||||||||
When you show an image of a western blot band, is the electrophoresis done on Tris Glycine gels? I'm concerned about the MW assignment (in this case 55kD) and I need to be sure it's based on TG gels otherwise it might migrate with my protein of interest (LDH-A, lactate dehydrogenase A), which runs just a tad lower than GAPDH. Thanks |
|||||||||
ANSWER: |
Thank you for your enquiry. I have confirmed with the originator of the product that the WB testing was performed using a SDS-PAGE gel. I hope this information will not hinder your experimental results. If there is anything else that I can help you with, please do not hesitate to contact me. |
||||||||
|
|||||||||
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Anti-Tubulin antibody (ab59680) at 4 µg/ml + HeLa cell lysate
Predicted band size : 55 kDa
Observed band size : 55 kDa
ICC/IF image of ab59680 stained HepG2 cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab59680, 1µg/ml) overnight at +4ºC. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
0
Call 01223 696 000 or contact us