I would like to know how to convert the gel image from black background to white background for publication.
Do you have "invert display" button on your gel image system? If you are using Bio-Rad, they have this function.
Which gel imaging system do you use ? you don't need to change the background the journal editor request it.
Easily done in The Gimp, free image software. Load your black background image in and press invert.
If you have Adobe Photoshop, you can save your image as tiff file and open in Photoshop. Under "Layers", click "invert" under "refine", your image will have white background.
I'd like to know if it is allowed to put an "invert display" gel picture on publicated paper?
Dear Pls, follow the link provided below to register to invaluable experiences in the face of COVID-19. https://swinuw.au1.qualtrics.com/jfe/form/SV_88qs1TRRQAv8Q9T
14 April 2020 191 3 View
I am working in ternary composites. Is there anyone working in graphene and its derivatives. I want to make a composite comprised of GO with some inorganic material.
05 May 2019 6,642 3 View
I need to dope metal to my metal oxide matrix, Can anyone clearly explain me about the calculations that i need to workout for mol %.
26 March 2019 1,277 4 View
Does the growth of microbes on ISP4 medium confirm the organisms to be a streptomycete? Kindly suggest some selection medium for Streptomycetes
17 February 2019 7,129 3 View
Usually the filter papers will be desiccated for 24 hr before and after ambient air pollutant sampling. As we encounter some error in weighing balance, we are unable to weigh the exposed air...
22 October 2018 1,718 4 View
I prepared nanorod structured undoped (pure) oxide thin film by spray pyrolysis method function of different substrate temperatures (STs). I found that decrease the bandgap when decreases the...
08 August 2017 5,868 21 View
25 May 2017 6,484 4 View
Similar to CONQUAS (Singapore) and PASS (HK), Is there any other quality assessement models available in the practice or in the literature domain?. Thanks Marimuthu K
26 October 2016 6,584 4 View
Im working on yeast secretary protein, my protein was his tagged so i use Anti-his monoclonal antibody for WB, i can see the signal but i got two band on each protein (totally i have two proteins...
16 December 2015 5,351 12 View
We isolated bacteria from various samples. It is identified by biochemical tests as Lactobacillus spp. Now we are going to sequencing it for species level identification. I'm a little confused...
29 March 2014 1,563 5 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 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 tried to separate my substance from a protein in a sillica gel column. By mistake, it dried and cracked. Can I save the trapped substance? Can I repack it ,or at least elute all of the trapped...
22 February 2021 1,789 3 View
This is gel electrophoresis result for total RNA samples with good conc. However, I guess there is a problem with the purity of the samples, i can't figure out why it appears like this? And how...
22 February 2021 338 9 View
Hi all, I proceed with nucleic acid gel electrophoresis recently several times, but a wried phenomenon is they always melted after running over 30min. My gel concentration is 1% percentage...
22 February 2021 9,896 3 View
I have cloned two domains of a gene into two bacterial vectors using cut and paste cloning with different RE sites. I checked the putative clones by colony PCR and Restriction Digestion (fallouts...
18 February 2021 6,736 4 View