Scientific misconduct and recent cases

I followed the first one about a Japanese researcher Haruko Obokata who was suspected of spiking her work with stem cells from other sources to suggest that she could induce inducible pluripotent stem cells iPSCs by stressing normal cells (or somatic cells).

Recently, another case in the US about a researcher Dong Pyou Han who spiked his rabbit blood samples with human antibodies to suggest that vaccine injected to the rabbits was able to induce immune response against the vaccine against HIV.

For the latest case, the perpetrator got a prison sentence.

XIST and pol III in XCI

X-chromosome inactive specific transcript (or Xist) is involved in X chromosome inactivation (XCI).
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Silencing or kd of Xist in somatic cells only produces low level reactivation in XCI.
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Those reactivated XCI transcripts are non-coding and upstream of the regulatory region contains SINEs (Short-INterspersed repetitive Elements targeted by RNA pol III).
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Involvement of RNA pol III?
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Kd of RNA pol III changed chromatin epigenetic landscape. A promising sign.
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Refers to work by Prof Zhang Li-feng (Nanyang Technological University)

Mnemonic for nucleotide nomenclature

This information is procured from "Nucleotide Nomenclature and Symbol" (In Biological Sciences).

Mnemonic for nucleotide nomenclature and symbol. The letters cap and underlined are the symbols. E.g. W represents Adenine and Thymine (or W = A or T), K represents Guanine and Thymine (K = G or T).

Information unfriendly commercial companies

I get it, that secret ingredients are what makes commercial companies thrive.
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Unfortunately, kits with minimal information is not helping students understand the concept behind workability of the kit (or approach). It is a disservice to Science and knowledge.
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I never liked companies that provided less-to-no information about their products. I shun away from these companies to save myself from being made into a technical person who follow instructions.
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Some companies are friendlier while others are protective of self-interest.
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For those who want to learn more about kits, the ideal place to look would be via patent files. Google is one place to start.
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Just to share.

Estimate the molecular/formula weight of DNA based on its length in base pair (bp)

This is just an estimation, i.e. 650.
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How to calculate Molarity and Number of DNA molecules

• Calculate the molecular weight of DNA molecule

A double stranded DNA of 100 bp will have an estimated molecular/formula weight = 100 bp x 650/bp = 65,000. Note that 650 is the molecular weight of one base pair.
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• Calculate the Molarity of DNA solution

To calculate molarity of DNA, e.g. 100 µg/ml (equivalent to 0.1 g/l) of 100 bp DNA will corresponds to 0.1/65000 Molar = 1.5 µM DNA (equivalent to 1.5 µmol/l).
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• Calculate the number of DNA molecules in a volume of DNA solution

To calculate the numbers of DNA molecules in 1 µl (equivalent to 1 x 10^-6 l) of 1.5 µM DNA, use the Avagadro number to convert mol to the number of molecules. First, determine the mol of DNA in 1 µl of 1.5 µmol/l DNA solution, e.g. 1.5 x 10^-6 x 10^-6 = 1.5 x 10^-12 mol. Next, determine number of DNA molecules, e.g. 1.5 x 10^-12 x 6.023 x 10^23 = 9.03 x 10^11 DNA molecules. That is equivalent to 0.9 trillion DNA molecules.
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• Calculate the number of DNA molecules based on mass

If I have a mass of DNA molecule, e.g. 135 pg of 500 bp dsDNA, how many DNA molecules is there? First, determine the molecular weight, i.e. 500 bp x 650/bp = 325,000. Note that 135 pg is equivalent to 135 x 10^-12 g. Next, determine the mol of DNA, i.e. 135 x 10^-12 / 325,000 = 4.15 x 10^-16 mol. In a mole, there is 6.023 x 10^23 molecules, thus the amount of DNA molecules is 4.15 x 10^-16 x 6.023 x 10^23 = 250 million DNA molecules.
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This is for my own reference.

Prevent autoclave water from seeping into pipette tip boxes

When I want to autoclave pipette tip boxes, I would place these boxes at higher level during autoclave. Placing these boxes (or other materials) near to the perforated platform just above the autoclave water would invite the "dirty" autoclave water (sometimes we tend to change the water once every two days or more) from seeping into the tip boxes. The brownish (probably due to spilt media) water will seep into the boxes and when dried, the tips will have a yellowish to brown stain covering them later.

When the tip boxes are placed neat to the perforate platform just above the autoclave water, then during the autoclave, the dirty water will thrash inside the autoclave and some of the water will seep into the tip boxes via cracks. That will contaminate these boxes.

The dirty water might contain impurities that will inhibit sensitive reactions or worst, contaminate stock solutions, enzymes, and expensive reagents.

Not all labs would use commercially packed filtered tips and we do use sterilized tips for dispensing expensive reagents. It is very important to properly autoclave tip boxes so that no contamination from the autoclave water will occur.

I had my fair share of dirty tips due to the above type of autoclave machine.

Just to share.

Inspiring story about Robert Langer

This is a story about Robert Langer,  "Engineer of Change" by TheScientist. 

At times, it's so challenging to stay in Science. If you don't publish, it's difficult to stay on to do research, as you might get penalized during job application or interview (for not having enough publications). I'm struggling with that now and it's demoralizing to get no rejection (no news).

I have to remind myself that it's all about having the right attitude (to get through the day). If indeed there is genuine love and passion for Science and the believe that our contribution will benefit mankind, environment and future, I guess going at different callings (opportunity that came knocking during the downs) will eventually lead us back to Science. For now, I'm applying for more options than just relying on research.

This article helped