How do I select best journal for publication?

The method of choosing a suitable publication has become more complicated as a result of the explosion of publications, specializations, and the rise of interdisciplinary topics. Until making a choice on when to write, authors must maximize against a variety of requirements or restrictions.

Which of the following factors do you most important to you to choose for publishing your research article(s)?

Hello,

I have a vapor production device that provides me with air+steam flow of 80% or 40% w/w (volume ratio) water vapor quality at 100 degC. The flow passes through a series of valves and tubes where it cools down because of heat transfer. There, the temperature is measured to be something around 50deC. I know that at 50degC, this amount of water vapor corresponds to super-saturated flow. So, I assume that the extra water vapor has been condensed inside the tube, and the resulting flow is a saturated vapor (I don't have access to see how much water has been condensed). Do you find this assumption realistic? Or I may be dealing with a super-saturated flow?

On the other hand, I am a bit uncertain about the measurements of the temperature sensor. To what extent, do you think that latent heat of condensation on the sensor can affect the temperature reading?

How to find a good journal to publish your work?

I am looking for useful proposals for doctoral research in the field of internal combustion engines (thermal engineering).

Which of the global publishing company is good?

Dear all

During reading in some papers about multiplex PCR primers, I have found some letters within the sequence as d, m, w and h which are referred to some bases sometimes one of three bases. The question here if I am going to request the same sequence which base I should add in stead of foreign letter or I have to try all till I got the one that give specific amplicon?

Thanks for your consideration

Best Regards

In the kit guide, it is mentioned that it is recommended to dilute the cDNA 3 fold before making a real-time PCR reaction setup.

Can I add 20 ul of nuclease-free water to 10 ul of cDNA to dilute 3 fold? Or I should add 90 ul of water and then I should take 10 ul of the final solution and add 90 ul of water to it again to make a 3-fold diluted cDNA?

Moreover, I am going to dilute cDNA for standard mix synthesis to use them in the real-time plate vessels. (S1,S2,S3,S4,55). I would like to know for diluting 1:10, 1:100, 1:1000, and 1:10000 of cDNA should I do serial dilutions?