What is the best way to obtain high-performance aptamers after performing sequence amplification by asymmetric PCR other than biotin and streptavidin?
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You could use a 5’ phosphorylated primer for the strand that you do not want then digest the product with lambda exonuclease then separate on non denaturing PAGE to get rid of the remaining dsDNA
Dear all. I'm modeling the RC column with cyclic displacement by Abaqus-Explicit. The concrete model used Concrete Plastic Damage model. However I'm facing with a error about the excessive...
01 February 2021 7,726 1 View
20 January 2021 7,043 2 View
Hello I recently am suffering calculation of temperature change resulted from the Joule-Thomson effect when propylene gas at 35 oC at 2 bar passes through a membrane to vacuum pressure (~ 0 bar)...
23 December 2020 4,091 2 View
Please, can the concentration of the drug inside the nanocarriers or nanoparticles be determined using a UV spectrophotometer after getting the calibration curve of the drug alone?
19 December 2020 4,634 5 View
I'm working with Herpesvirus and Adenovirus. For Herpesvirus, I use Vero cell line to activate and check virus titer. For Adenovirus, I use Hela cell line. Recently, I could activate them, but...
16 December 2020 4,073 5 View
If possible, let us know about the which vaccine would be available in your geographic location.
06 December 2020 3,527 23 View
Nowadays I have received a lot of invitations for attending conference online like webinar and get certificate and I am wandering about this certificate is the same for real attendence physically...
26 November 2020 5,344 4 View
I read some publications stated that the value of enthalaply change higher than 40 kJ/mol the adsorption will be chemisorption and below this value will be physisorption he negative values of...
22 November 2020 8,353 5 View
there many analyze to determine the exact size of the synthesized nanoparticles which is a more accurate TEM or XRD data analysis
05 November 2020 9,736 11 View
Make no mistake that journals indexed in reputable databases such as Scopus can be considered legit by default. Your contribution sure whets your appetite for learning which venue should...
27 October 2020 246 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
Hello, We would like to increase the yield of our PCR product. We are running a series of PCR reactions that is targeting ~1.1kb sequence. We begin each reaction with ~400pg of template DNA...
02 March 2021 4,029 3 View
I am going to have 3 different probes in my qPCR work that I am going to do. But I realized that the machine we have in the lab is a Rotor-Gene Q 2plex HRM Platform, saying it has green, yellow,...
01 March 2021 8,544 1 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
Does anyone have the experience of using Taq Man probes in the QIAGEN Rotar- Gene qPCR machine?
01 March 2021 5,311 1 View
I have used an AllPrep DNA/RNA/Protein Mini Kit QIAGEN kit to extract RNA and protein from my samples. At the end of the protein purification, I resuspend my protein in 5% SDS. Will these samples...
28 February 2021 7,370 3 View
Dear All, mirna primer showing some problem in the melting curve? any idea why? As attached is the melting curve. The forward sequence is obtained from miRBase and reverse primer is universal.
28 February 2021 5,008 4 View
I performed site directed mutagenesis, transformation, and then I sent out plasmids for Sanger sequencing and found out that there is extension of DNA just before the stop codon. I am not sure...
27 February 2021 547 3 View
Hi, my question is about the heating of thermal cycler machines and I hope some of you had experienced a similar thing previously. There are two thermal cycler machines in the lab(BioRad) and for...
26 February 2021 4,777 4 View
Hi I am a bit confused. They are asking me to find out the volume of DNA required in ul (a total of 30-100 ng for genomic DNA) from the DNA concentration in the nanodrop reading which was 404.8...
26 February 2021 5,029 2 View