Hi every one, I am going to prepare a TBE buffer, and the EDTA preparation takes a long time, so can I keep the EDTA without autoclaving for a long time until I get ready to do so.
Hi Muna, Yes, you can
Hello. I run my Abaqus simulation in the supercomputer and once it's done, I copied the result (odb file) into my local computer using winSCP. But I faced a problem to read that file (see...
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Does the H-Index for researchers appear on the Scopus website without activating or doing anything by the researchers?
17 November 2020 3,849 5 View
dear Colleague I have research with my students about ABO groups and Anemia. Is there relationship between both of parameters? what your opinion and do any have references because we looked for...
09 March 2020 8,528 11 View
The scientific basis for choosing the idea of research with the lowest probability of expected errors.
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Effects of different media composition, light intensity and photoperiod on the morphology and physiology of freshwater microalgae Ankistrodesmus falcatus - potential strain for biofuel production
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This is my graduation project subject and I want your advise and recommendations of the experimental procedure.
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How can we analyze the qualitative data from a semi structured interview? and how much the sample size needed for ethnographic qualitative research?
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Hello! I want to quantify by ELISA the secreted (from platelets poor plasma) and the non-secreted (from platelet lysate) PF4 before and after TRAP stimulation. I will use the ELISA from R&D...
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Results of single-case research designs (i.e., n-of-1 trials) are often evaluated by visually inspecting the time-series graph and computing quantitative indices. A question our research team is...
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Hello, If i am doing a buffer exchange for an antibody of 1mg/mL, does the elution lose protein in the process of buffer exchange? For example, if i flow through 500 uL of 1mg/mL sample, and...
03 March 2021 6,299 3 View
Hello! I'll do a size exclusion chromatography, but I only have an open column, and I'll perform the peptide extraction from yeast, using buffer lysis (sodium phosphate 50 mM/NaCl 30 mM/DNAse and...
01 March 2021 2,215 2 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
To dear Researchers, I was analyzing a series of concentration for estimation of Real-Time PCR efficiency. The concentration was 1:10. I used MS-excel to evaluate Slope. The result of slope was -8...
01 March 2021 8,683 4 View
I'm looking at the aggregation of my protein sample using DLS. Unfortunately, my buffer (20mM HEPES) also results in a set of peaks. These are at approximately 1 and 1000 d.nm. The lowest peak...
01 March 2021 9,015 2 View
I want to use 0.1% gelatin. Should that be made in PBS or sterile water? Should I autoclave the gelatin soln after making it in water/PBS?
28 February 2021 274 2 View
Is the period to autoclave not enough? The inoculation in a hood and flame and UV and alcohol.
27 February 2021 9,356 3 View
I need to extract protein from fermented carbon sources for Bradford assay. Most researchers experiencing insolubility of pellet in resuspension buffer. Please assist me to select most suitable...
26 February 2021 7,129 3 View