I am facing problems sequencing a clone, in vector p.CDNA3.1.

More Anjali Mann's questions See All

Can anybody help me with an efficient way to de-protect poly(tert-butyl norbornene-2-carboxylate)?

I want to make poly(norbornene 2-carboxylic acid), for the sake of characterization, I decided to start with the protected monomer norbornene-tert-butyl-2-carboxylate for the ring-opening...

03 December 2020 3,852 5 View

Why Schiff bases change colour upon evaporation?

I got bright yellow coloured Schiff base after 6 hour reaction time. So i kept it for slow evaporation. Solvent was methanol. But after complete evaporation my product colour changes from yellow...

17 November 2020 3,824 2 View

Has anyone observed delamination of pyrolysed SU-8 on SiO2 coated Silica substrates when the pyrolysis is performed outside cleanroom?

We have a quartz tube furnace (diameter 80 mm) outside the cleanroom and when tried to pyrolyse the SU-8 on SiO2 coated Si substrates at 900 C in nitrogen atmosphere, the electrodes looks fine....

08 November 2020 4,357 2 View

Is there any chance for synthesis Schiff bases using 4-methyl-5-imidazole carboxaldehyde?

Is there any chance for getting product using the above aldehyde and different amines.

12 July 2020 8,330 2 View

Can anyone help me finding good impact factor journals to submit uninvited review paper on postharvest chilling injury in fruits.?

I have tried submitting my review paper in relevant journals, but most of them only accept the review paper invited by the editor of the journal

28 June 2020 4,371 5 View

In simple terms what is the difference between light cone quantisation and light front quantisation?

Susskind in his paper "The World as a Hologram" uses the term light front quantisation. I know only of light cone quantisation, hence this question. I am trying to see the connection between...

19 May 2020 832 3 View

What is an alternate way to recover a polymer product from DMSO or DMF other than evaporation?

Due to the high b.p of DMSO and DMF (189 and 153 degree Celsius), it is difficult to recover my polymer from the solution. I believe extraction in a triple system (such as DCM, DMSO and water)...

04 March 2020 3,028 12 View

What were the active sites on the magnetic activated carbon surface for adsorption of reactive dyes? Were they carbon atoms or Fe3O4?

In the adsorption process by using adsorbent magnetic-activated carbon for removal of reactive blue 13 dye which contains -N=N- group, SO3 group, OH, Cl, etc. In this process what are the active...

24 February 2020 1,110 4 View

Why i am getting only one peak at 280 nm for dyes ?

I prepared aminobenzothiazole reacted with amino phenol azo dyes but on taking UV I got single peak. Why I couldn't get 2 peaks?

18 February 2020 6,949 3 View

Could anyone please help me to get my schiff base product?

Hereby I am explaining the detailed procedure which i done in my lab. 1:1 molar ratio of 2-amino benzothiazole and 4-nitro benzaldehyde were refluxed for 12hr at 100 degree Celsius in toluene...

24 January 2020 5,094 3 View

Enhanced Yellow Fluorescent Protein (Aequorea victoria) DNA sequence?

I am on the lookout for the Enhanced Yellow Fluorescent Protein (Aequorea victoria) DNA sequence. Does anyone know where I can find it? Thank you in advance

03 March 2021 3,568 1 View

Can linear DNA be used as template for site-directed mutagenesis?

Is it possible to induce site-directed substitution mutation by quick-change method on linear dsDNA? or it has to be cloned in some vector? If yes, should it be treated with the Dpn1 enzyme...

03 March 2021 401 4 View

Does anyone have a recommendation for yeast reporter gene plasmid/protocol?

Hi, could anyone recommend a plasmid and/or protocol for reporter gene assay in S. cerevisiae? I want to assess the effect of growth conditions on a transcription factor, so I want to clone it`s...

01 March 2021 210 1 View

Is it possible for two human neuronal cell lines to have different gene sequence for the same protein?

I am looking at the ATP1A2 (Sodium/Potassium ATPase alpha subunit 2) in two human neuronal cell lines. Expression levels of this protein seems to be almost equal when detected by one antibody....

01 March 2021 3,607 3 View

Expression cloning by using cDNA,do I need to modify the cDNA first?

I am going to have a expression cloning of mammalian gene by using shuttle plasmid to transforming the E.coli However I don't know I should only inserting the Coding sequence ,or I can...

28 February 2021 5,440 3 View

Genome-wide gene identification protocol ?

Is there any book chapter/book, webpage or research article available to understand genome-wide gene identification?

28 February 2021 8,095 1 View

Can anyone provide the Support vector regression code structure of LIBSVM MATLAB or python ?

Please, if Gaussian Parameter optimization is possible in this code structure

28 February 2021 278 3 View

Any specific pipeline or parameter to analyse total transcriptomics study of brain tissue samples?

I have two groups of brain samples, control and treated for example. It was total RNA nova seq sequencing. I tried all the available pipeline like: star+rsem+deseq2, Hista+stringtie+cuffdiff,...

27 February 2021 356 6 View

Runs of nucleotides in Sanger sequencing?

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

Has anyone used the Illumina ITS1 primer sets?

Hi everyone, Illumina provides a list of primers to amplify with high taxonomic coverage the ITS1 region for further fungal sequencing, but I cannot find the exact amount necessary of each...

25 February 2021 6,969 3 View

Abel Tan

What do you mean plasmid performs good? Sufficient amount? Purity?

Are you outsourcing or doing sequencing in house?

Paul Rutland

can you post an .ABI file of the failed sequencing please.They contain a lot of useful information. Are all of your sequences failing and have you checked that the primer sequences exist in your vector. Are you sure that your sequence is in the vector on the samples that you are sequencing