We tried to isolate plasmid by Alkali Lysis method. In the circled region we could not visualize so what may be probable reasons for that
Possibly when you washed the precipitated plasmid the dna pellet was not sufficiently well centrifuged and it was lost in aspiration or tube inversion
Today there is a great push for GMO technology as it seems to be marketed as something that has the potential to address major world problems including world hunger, food security, etc. However,...
07 September 2022 5,190 5 View
Hello everyone, I have did EIS test on substrate steel of GI steel and GI steel using CorrTest software. I have obtained the Nyquist plots and Bode plots, but the surface of the exposed area to...
16 November 2020 2,507 6 View
Please give your opinion on these connectors. Are these connectors useful for a 1 to 40 GHz printed monopole antenna with tapered microstrip feed width varying from 2.95 mm to 1.6 mm. Substrate...
15 September 2019 7,141 3 View
Can any one please tell me what should be the minimum/maximum distance between two identical super wide band antennas to measure group delay, isolation (both magnitude and phase) and fidelity...
09 September 2019 6,211 5 View
I have designed and simulated a super wideband antenna in HFSS. Simulation results gave a bandwidth from 2.2 GHz to 30 GHz for S11 < -10 dB and other results are also good. A lossy FR4...
04 September 2019 3,816 4 View
Can any one please tell me how to model and simulate SMA connector in HFSS as shown in the attached file. Thanks and Regards, Srinivasarao Alluri.
12 March 2018 7,642 4 View
I have designed a super wideband antenna having 1 GHz to 40 GHz bandwidth using HFSS and i got simulated results. Now i would like to fabricate and make some VSWR, input impedance, radiation...
04 March 2018 1,133 6 View
Practically in antenna design patch, feed and ground are made with copper sheets with non zero thickness. what is the thickness of copper used for ground, patch and feed in antenna design if the...
03 March 2018 2,552 9 View
I am trying to do immuno-precipitations in denaturing conditions. One protocol I have says denature in a buffer with 1.85 M NaOH + 7% β-Mercaptoethanol, then precipitated with 50 %TCA. Again the...
08 May 2016 3,554 3 View
Hi all, I have a query I completed docking with Auto dock vina in Windows machine. I want to visualize interaction (hydrogen) bonds between ligand and protein after docking with Auto dock vina. I...
12 June 2015 3,757 5 View
I'm cloning a fragment of 3200 nts into plasmid. The cloning was successful, however, 02 amino acids were mutated. Now I want to fix these 02 aa by site-directed mutagenesis technique using...
08 August 2024 4,645 2 View
Hi all, I need to introduce an ARS (autonomously replicating sequence) in my plasmid but I'm not sure which position would be the best. Does anyone have any suggestion? A picture of the plasmid...
05 August 2024 1,573 4 View
I want to introduce a point mutation (change in one nucleotide) into my gene of interest (DNA binding domain) I have designed primers as recommended on the Data sheet of the kit : -Both primers...
05 August 2024 9,059 3 View
I am performing ligation of the plasmid and a target gene. The steps I have taken are: 1. Double digestion of the plasmid and target gene 2. Ligation of the plasmid with the target gene 3....
05 August 2024 2,570 3 View
Dear All, I am trying to transfect a pCDNA3.1 vector containing my gene of interest. The purpose is to figure out the localization of the protein of interest. I have fused the protein with GFP on...
31 July 2024 9,892 4 View
Hello I am trying to create a stable cell line in HEK293 via Lipofectamine 3000 transfection. My plasmid is a CD63-IL10-GFP construct with Puromycin resistance. I am successful with the...
30 July 2024 6,648 1 View
I have been trying to electroporate SKOV3 cells with a large plasmid (11kb) without much success. Any tips?
29 July 2024 3,229 1 View
I created two potential gene expression cassettes (constitutive and inducible) for expression of a mutant PETase gene on PeptiCloud using the version tree feature, which allows users to create...
28 July 2024 7,559 1 View
Please address the best way to drop a plasmid. Background: I have a "bait" plasmid resistant to kanamycin and a "prey" plasmid resistant to carbenicillin. After many rounds of streaking on...
25 July 2024 2,532 3 View
I am currently at a stage in my research where I will be using the pLV6-Bmal-luc plasmid (Addgene #: 68833). However, I am encountering some issues with the isolation of this plasmid and am unable...
23 July 2024 5,296 0 View