The current pioneer project incited from the combination opinions, thought, research efforts and long experiences on the related fields by our team colleagues above. The presence of natural antimicrobial activities presents in the CM, which is almost 10 folds more than the cow’s milk, and/or other types of animal milks. It is quite known that CM is highly close to human mother’s milk and considered as supper food and white gold for its nutrient’s beneficial properties [1-3]. This shows for us a golden opportunity to be tested innocuous natural treatment for patients with COVID-19 infection [4,5] It has been shown that in many countries of the Middle East, Africa, and Asian countries, that they use it very frequently as natural nutrients, also as medication beverage for their health benefits [5-6]. The Camel Milk (CM) contains rich therapeutic biocomponent nutrients, such as vitamins, electrolytes, peptidoglycans recognition, lactoferrin, and lysozyme. Also, has potential effect in treating many wellknown diseases such as Diabetes Mellitus, allergies, autism, crohn’s disease, viral hepatitis, malignancies, anti-infectious, and auto-immune diseases. All these medical properties attract us to try the natural CM or their bioactive products as an excellent option to treat the Covid-19 [7]. On the other hand, some interesting publication reports demonstrated that camels are host to show good immune response to MERS-2 virus, their essential immune defense factors made us focus on the rare immunological natural existence and high affinity activity of the unique mono heavy chains of the CM Nanoimmunoglobulins (nIgs), which can easily pass through the whole intestinal ducts, kidney basement membranes (glomeruli), and brain tissues. Also, have supper antiviral activity (ies) [8]. These interesting molecules are stable at high temperature, can neutralize viruses in infected cells, resist to the activity of digestive enzymes in stomach, can easily pass through the whole intestinal ducts and have high affinity against many other germs [9]. All these extra characteristics of the CM together brought up the idea of building up this project to hopefully applying it in vitro and in vivo as a natural therapy against the most dangerous virus worldwide in the last 100 years ago, which is called the MERS-Covid-2 or Covid-19 by the WHO [10].

Most of the tropical neglected diseases casing agents are single celled eukaryotic parasites that affect millions of global populations physiologically, economically and sociologically. These diseases not only affect humans but also affect the animals that sustain life within these populations completely influencing the societal fabric on sustenance. The current therapies are limited to poorly selected drugs that have a poor efficacy and extreme adverse effects. The current quick growth in sequencing and atomic structure determination of the parasites cellular organelles has accelerated the venture to obtain newer intervenes that would serve to benefit these populations. The rapid in silico determination of the ribosomal structure, specifically the 18S rRNA has revealed the mechanisms by which some therapeutics induces their effect on the process of translation to the parasites. We show some in silico atomic resolution structures of 18S rRNA of neglected tropical diseases. We further show strategies and scenarios that are exploited to interfere with translation, thus highlighting the 18S rRNA as a primary drug target. The results also highlight unique as well as conserved elements in binding pocket that can serve as hotspots for novel therapeutics development.

A versatile programmable tool for effective and precise genome editing and gene targeting has been utilized and prepared with normal Clustered regularly interspaced short palindromic repeat-CRISPR-associated protein (CRISPR-Cas) genome editing, a prokaryotic adaptive immune system. This ground breaking approach can be used for the treatment, detection and treatment of cells, in vivo gene therapy or animal models. Safe and effective provision of CRISPR/Cas9 remains one of the biggest therapeutic problems in recent years. Though in-vivo and in-vitro genome editing have many advantages, their severe obstacles, such as small insertion sizes, high risk of carcinogenesis, and stimulation of the immune system are causing many problems for laboratory and clinical applications. The power of the latest cancer therapeutic approach has been shown by the genetically engineered immune cells using chimeric antigen receptors (CAR) or modified T cell receptors (TCR). While Autologous CD19 CAR T cells are effective in their clinical development, they have many advantages over their autologous counterparts, and recently, due to the advent of multiplex genome editing techniques, in particular CRISPR/Cas systems, have gathered wide-ranging attention.

Microarrays are utilized to study the declaration of thousands of qualities in a solitary analysis. Applied inventively, they can be utilized to test just as create new speculations. As the innovation turns out to be more available, microarray examination is discovering applications in assorted spaces of science. Microarrays are just a strategy for imagining which qualities are probably going to be utilized in a specific tissue at a specific time under a specific arrangement of conditions. The yield of a microarray try is known as a "quality articulation profile."

In vitro ribosome development could empower investigations of ribosome get together and work, give a course toward building insignificant cells for manufactured science, and grant the development of ribosome variations with new capacities. Toward these drawn-out objectives, we as of late wrote about a coordinated, one-pot ribosomal RNA blend (rRNA), ribosome gathering, and interpretation innovation (named iSAT) for the development of Escherichia coli ribosomes in rough without ribosome S150 removes. Here, we planned to improve the movement of iSAT through transcriptional tuning. In particular, we expanded transcriptional effectiveness through 3′ alterations to the rRNA quality groupings, upgraded plasmid and polymerase focuses, and showed the utilization of a T7-advanced rRNA operon for stoichiometrically adjusted rRNA blend and local rRNA preparing. Our alterations delivered a 45-crease improvement in iSAT protein blend movement, empowering combination of 429 ± 15 nmol/l green fluorescent protein in 6 h cluster responses. Further, we show that the translational movement of ribosomes decontaminated from iSAT responses is about 20% the action of local ribosomes cleansed straightforwardly from E. coli cells. Looking forward, we trust iSAT will empower extraordinary examinations to disentangle the frameworks science of ribosome biogenesis and open the best approach to new techniques for making and contemplating ribosomal variations.

Advanced transcriptomics with pyrophosphatase based super high throughput DNA sequencing of di-labels gives high affectability and practical quality articulation profiling. Test readiness and taking care of are incredibly improved contrasted with Serial Analysis of Gene Expression (SAGE). We analyze Deeps AGE and Long SAGE information and show more prominent force of recognition and multiplexing of tests got from potato. The record examination uncovered an extraordinary plenitude of up-controlled potato records related with pressure in lethargic potatoes contrasted with collect. Critically, numerous records were distinguished that can't be coordinated to known qualities, however is probably going to be important for the abiotic stress-reaction in potato.

The Array Express Archive is one of the three worldwide public stores of utilitarian genomics information supporting distributions. It incorporates information produced by sequencing or exhibit based advancements. Information is put together by clients and imported straightforwardly from the NCBI Gene Expression Omnibus. The Array Express Archive is firmly coordinated with the Gene Expression Atlas and the succession information bases at the European Bioinformatics Institute. Progressed questions gave through philosophy empowered interfaces incorporate inquiries dependent on innovation and test ascribes like infection, cell types and life systems

A total of 50 clinical samples were taken from the blood of typhoid fever patients who visited Al-Hillah Surgical Teaching Hospital and private laboratories in the AL-Hillah/Babylon region between February and August 2021. This research included 50 people who looked to be healthy and diseasefree. Individuals with genotype GA were significantly represented among the patients with typhoid fever: 33 (66%), P-value = 0.0030, as compared with healthy control subjects, 18 (36%), and had an increased risk of developing typhoid fever infection. The IL-1beta (G) allele was less frequent among patients (51%, n=51) than control, and the (A) allele was more frequent among patients than control (49%, n=49). The results showed that there was a significant association between GA genotype and typhoid fever under most inheritance models. The A allele represents a risk factor for patients with typhoid fever and the inheritance of codominant, dominant, and overdominant models as risk factors. The GA genotype has an odd ratio of 4.07 (1.54–10.79) in the model of inheritance. Codominant and dominant models have a related odd ratio of 3.04 (1.21–7.60) and the overdominant model has a related odd ratio of 3.45 (1.52–7.85). A highly interesting Nucleic Acid Polymorphism (SNP) was detected in this study in the investigated samples, in which guanine was replaced with adenine at position 122, namely G122A for the IL-1beta gene

Transposable elements are repetitive sequences widely present in eukaryotic genomes, embedded in the heterochromatin-the tightly condensed chromatin-which prevents their transposition. The unscheduled transcription of transposons and its harmful consequences have been proven to play a role in neuron degeneration. Drosophila models are crucial to unveiling this role and the mechanisms triggering transposon activity. Specifically, abnormal heterochromatin relaxation, which is also observed in Alzheimer’s disease, has been found as the key event leading to transposon “escape” in the brain. This review recapitulates the main efforts towards demonstrating the role of transposons in neurodegeneration focusing on drosophila models, and offers an integrated overview of common and specific molecular mechanisms useful for identifying new therapeutic targets.