Why should we make agarose gel by hand and no sell?
Is it related to properties of gel?
Hello, I have read some papers about hematologic malignancies. And, I wondered why investigators compare short-term infusion and continuous infusion during phase I study. And also, I wondered why...
03 April 2018 1,966 3 View
Are acetone, methanol, and ethanol proper as cleaning agents for glassware? In addition to volatility, solubility, and low cost, what kinds of reason that ensure them as good cleaning agents?
07 August 2017 2,544 3 View
We mainly use endotoxin-free kit for plasmid preparation due to disturbance of LDS. But there are also non-endotoxin-free kit. Why do we use it? I think that non-endotoxin-free kit is cheaper than...
07 August 2017 1,401 3 View
When we prepare plasmid DNA with some tools like maxi prep., endotoxin-free is very improtant. In terms of transfection efficiency, I guess that LDS may compete with DNA as transfection reagents,...
07 August 2017 5,398 5 View
I have studied translocation of exogenous DNA during transformation of E.coli But, I cannot understand homologous recombination of ssDNA and relationship among RecA, DprA, and ssDNA Can you...
07 August 2017 456 1 View
If we extract protein in heads of flies, we homogenize the heads and put LDS buffer and reducing agents. And then, we put them in heating block Why do we heat the homogenized heads in heating...
06 July 2017 7,050 2 View
06 July 2017 933 1 View
Hi, I have problems with running gel electrophoresis. I have tried agarose gel electrophoresis and native PAGE. I have two proteins, which have molecular weights of ~30kDa and ~180kDa and two...
03 March 2021 4,275 4 View
Gel electrophoresis, RNA degradation, RNA extraction from fresh tissue
02 March 2021 5,433 5 View
I'd like to perform single-strand conformation polymorphism (SSCP) in my thesis, however I cannot control the temperature of the vertical PAGE since we are using the conventional tanks. Is there a...
02 March 2021 9,157 1 View
Can someone please give me some possible things that could go wrong? Here is my recipe: 0.5g Agarose 50 mL of TAE 1x 1 uL ethyl bromide. Gel was run at 100V for 1 hour. The buffer used is also TAE.
01 March 2021 9,952 3 View
Hi, I am running a size exclusion chromatography experiment with a buffer containing Potassium Acetate as a salt. I analyse these fractions through SDS-PAGE. After boiling my SEC fractions in...
01 March 2021 2,622 3 View
I am trying to classify and analyze the results of an SDS-PAGE based array for bacterial detection using machine learning, but I have trouble finding the best way to represent the results with...
27 February 2021 9,176 3 View
I am worried about this overexposure of the upper part of the gel in the picture. Is it possible that this is the result of too much concentration of ethidium bromide? Why is there such a big...
25 February 2021 8,140 3 View
I'm running an EMSA to show the DNA binding activity of recombinant proteins versus the Wild type. Previous assays run by my research group using a different test system show the protein-DNA...
24 February 2021 8,325 1 View
I am trying to clone 2 copies of the same mammalian gene into the pSF-CMV-Ub-Puro Ascl (contains HindIII, KpnI and NheI cut sites) plasmid. This is what the final product is supposed to look like...
24 February 2021 6,310 3 View
Hi Everyone, I am a bigginer in western blotting and I am trying to use it for validation of my proteomics data. I have: two regulated proteins with molecular mass of 40 and 73 kDa one control...
23 February 2021 6,671 4 View