as i cloned promoter region in topo vector but somehow only 18oobp region was cloned instead of 2000bp
Was the band you cut out of your gel definitely 2kbp long? have you checked other colonies?
How did you initially check your TOPO clones? Keep in mind that if you do PCR with the M13F and R primers those sites are offset from the MCS and will add 200 bp of length to your fragment.
Robert Adolf Brinzer Thak you! yes, I did. Amy Klocko Thank you.
I am trying to perform the quantitative analysis of minerals in my samples. I have the XRD raw data of my samples. I started Rietveld refinement in X'pert Highscore and Match!* software but there...
22 April 2024 9,318 5 View
How to check LAB6 filament running hours in JEOL 120KV 1400. When we can say that the filament has blown off?
02 November 2023 402 1 View
How can we perform a quantitative analysis of the XPS peaks using Origin software? Please help, How can we do a quantitative analysis of each peak? The peaks of C1s are attached below.
31 October 2023 5,330 4 View
Can anyone please help me with how I can get the quantitative (mol%) value of any sub-peaks that are part of the main peak, such as N, C, and O?
26 October 2023 6,307 6 View
While conducting the similarity check, I have already excluded the bibliography and quotes. However, references after sentences are still appearing in the similarity check. How can I exclude...
25 August 2023 7,240 0 View
Recently, we conducted DSC experiments on various glassy alloys within the SeTeSnIn system. I have provided the attached DSC scans for your examination. Similar DSC scans were obtained at...
20 July 2023 2,099 3 View
I have X'pert high-score software for XRD analysis with PDF2 Database, please help me regarding search peaks section.
16 June 2023 6,447 6 View
Running coupling constant is always written as a function of momentum. Is it possible to write in terms of interquark separation distance? If so, what will be the formula?
13 June 2023 7,594 0 View
In mathematica, after I solve Schrodinger equation using Matrix Numerov method, I am getting pure numbers as eigenvectors. Is it possible to get pure numbers as eigenvectors? Now if I want the...
15 May 2023 8,075 0 View
Please provide me original literature or reference material for the given equation. Vitrinite Reflectance (Ro) % = -2.712 * log(V.M.) + 5.092 Where V.M. is on a dry ash-free basis.
27 April 2023 6,482 6 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, everyone. I want to transfer two genes in to the pseudomonas bacteria that isolated from the soil. The bacteria that I want to use for cloning haven't been identified and not be sequenced,...
02 August 2024 3,987 1 View
Hello, We found three packages of Illustra™ MicroSpin™ G-25 columns in the cabinet of an unused lab. They are very old but have never been opened. I have never used this kit before, and I couldn't...
25 July 2024 4,927 3 View
I am cloning an overexpression plasmid with my protein of interest tagged with mScarlet. After transforming my ligated product into DH5α bacteria and plating on LB agar, I noticed colonies with a...
22 July 2024 5,953 6 View
through genetic modification or metabolic engineering? Is it helpful, good for health ?
22 July 2024 7,811 4 View
I have immunized BalB/C mice with a protein using the intradermal (ID) method with Complete Freund's Adjuvant (CFA) and Incomplete Freund's Adjuvant (IFA), following a 14-day interval and three...
22 July 2024 9,160 2 View
hi every one I am making vector construction (for fusion proteins) and in this moment I wanna to amplification of ADAM17 prodomain with PCR. to yet, I couldn't amplified the ADAM17 prodomain with...
21 July 2024 8,660 1 View
I am treating human cells with an AAV vector encoding for my gene of interest tagged by FLAG. I want to quantify the mRNA expression of my gene of interest via qPCR to discriminate the endogenous...
14 July 2024 8,482 3 View
As flaviviruses genome is very frequently prone to mutation hence it is very difficult to clone whole genome inside vector what kind of vector and cells can sustain such amount of cloning...
11 July 2024 4,284 0 View
I am working on cloning of a gene fragment inside my vector everything we tried to do correctly like making insert and vector with utmost care but after ligation the morphology of colonies seems...
11 July 2024 9,010 3 View