I got dark background
proteins are not visible
Following Silver-ammonia method
Hi Urooj
Is it for staining protein in a SDS-PAGE gel? If yes, do you cast your own gels or do you use pre-cast commercial gels?
For silver staining you need to have very well cleaned glass plates and other material!
I am doing native PAGE gel for enzyme proteins
Be sure to have all glass equipment absolutely clean. Soap, ddH2O and ethanol or acetone.
Maybe the concentration of substrate for the enzyme reaction is too high.
Meet me
Here are my recommendations:
1. Use fresh SDS running buffer
2. Use only mQ water or dH20....avoid tap water for cleaning
3. minimize hand contact (or glove contact) with the gel...in other words, do not touch gels!
4. Check your sample buffer for possible protein contamination....if possible, use fresh one.
Staining methods
08 September 2014 152 4 View
02 March 2021 3,060 3 View
I took measurements of different concentrations of 15 nm and 5 nm Au nano particle solutions. I'm trying to determine which concentration I measured gives the best reading overall. I also...
02 March 2021 7,626 1 View
Hello Everyone. Currently I am working to characterize macrophages in the myocardium after ischemia-reperfusion injury in rats. Due to the low total cell number isolated from rat hearts I can...
01 March 2021 3,867 3 View
We are preparing some experiments based on irradiating cells under different conditions in order to evaluate the effects in terms of DNA damage, genetic expression, etc. As our project is...
01 March 2021 3,355 3 View
In the stabilization of AgNPs are vital in current research interest. However, some of the 2D nano-materials like graphene oxide, MoS2, etc... previously used to stabilize it. But still they shown...
01 March 2021 2,207 3 View
I am looking at the ATP1A2 (Sodium/Potassium ATPase alpha subunit 2) in two human neuronal cell lines. Expression levels of this protein seems to be almost equal when detected by one antibody....
01 March 2021 3,607 3 View
Also when RHAMM binds hyaluronic acid, they get internalized, will RHAMM also be degraded? Or both CD44 and RHAMM will be transferred back to the cell membrane? Asking for breast cancer cell line...
01 March 2021 8,169 2 View
I'm a student and I have to produce a cell line with a knockin for the NRF2 gene with GFP. I have to put a promotor in front of the GFP because the gene will be too far away from the promotor of...
28 February 2021 7,127 2 View
Interested to stain mice brain tissue with WGA 488 conjugate, appreciate if anyone willing to offer me some guidance or suggestions! Thank you!
28 February 2021 3,951 2 View
Im doing PBMC isolation -> CD14+ enrichment using magnetic beads -> stimulation setup. My negative control is just cells in cRPMI but they seem to get activated over and over again.
28 February 2021 7,883 3 View