Відео

You're most welcome

Thank you for your kind words. Keep watching

Thank you dear

Thank you dear❤️❤️❤️❤️

Thank you for your kind words. I am glad that it was helpful

Thank you for the nice comment and Most welcome. I'll upload the next video in 3 to 4 days

You're welcome!

I agree that the procedure is painful

Thank you dear

Thank you dear

Thanks a lot dear 😊

Thank you so much for your incredibly kind words. It's truly heartwarming to receive such appreciation for my teaching efforts. I'm delighted to hear that you find my dedication and motivation inspiring, and I'm honored to have made a positive impact on your learning journey. Your commitment to learning and your generosity of spirit shine through in your comment. It's students like you who make teaching such a rewarding profession. While the idea of teaching you the whole science sounds like an exciting prospect, remember that the greatest reward for any teacher is seeing their students succeed and thrive in their endeavors. Your determination and eagerness to learn are what truly matter. I look forward to continuing this journey of knowledge and discovery together. Thank you once again for your kind words and encouragement.

This is the quickest way to do it dear, practice it a lot and you will be able to solve your exam question in a minute

@@learnbiotechnologyandmicrobiol Okay 👍. Thank you very much for this video. It’s very helpful I understood what to do.

@@ShivenStudy Most welcome. If there are any further questions or queries, you can contact me anytime

Thanks dear

Thank you so much 😊

Yes there are some differences between protein and DNA microarrays and I will soon make a video on DNA microarray. The basic difference is DNA microarray is an arrangement of DNA spots (in picomole) attached to a solid surface for the detection of DNA (gene) while in a protein microarray, collection of purified proteins, antibodies, affibodies etc are attached on a solid surface.

You are most welcome dear

Thank you dear

Thank you dear

Thank you

Thanks dear 🙂

Always welcome dear

You can contact me via email at ibrarkhan1984@uop.edu.pk

You can also contact me via WhatsApp at 00923315818733

Thank you😊😊😊😊

Thankyou so much

Check it tomorrow. I will upload the subtitles today and you can use the translate option

تحقق من ذلك غدًا. سأقوم بتحميل الترجمة اليوم ويمكنك استخدام خيار الترجمة.

يمكنك الآن استخدام خيار الترجمة في يوتيوب للحصول على ترجمة باللغة العربية

Yes, you are tight

Thank you

Thank you for the nice comment. Centrifugation served two main purposes in their experiments: 1. Initially, as the bacterial culture was grown in a liquid medium, they aimed to isolate the bacterial cells from the media. Centrifugation was employed to separate the denser bacterial cells, which formed a pellet, from the lighter media found in the supernatant. 2. After cell lysis, centrifugation played a crucial role in segregating cell debris and unbroken cells from the cellular components released during the lysis process. The answer to your second question is: After employing mechanical and enzymatic treatments, a homogenizer was used to further break down the cells. I hope this answers your questions. Feel free to contact if there is still any query

The levels of hemoglobin A2 (HbA2) and hemoglobin F (HbF) are relevant in the context of diagnosing certain hemoglobinopathies, including sickle cell trait. In a normal, healthy individual with no hemoglobinopathies, the typical hemoglobin composition is primarily hemoglobin A (HbA). Hemoglobin A2 (HbA2) is a minor component, usually making up less than 3.5% of total hemoglobin. Sickle cell trait (HbS/HbA) is characterized by the presence of hemoglobin S (HbS) along with hemoglobin A (HbA). In individuals with sickle cell trait, the level of HbS is typically less than 50%, as it is a heterozygous condition. Looking at your question values: HbA2: 3.1% HbF: 0.5% These levels are within the normal range for HbA2 and HbF. Based on these values alone, it doesn't suggest a diagnosis of sickle cell trait. However, it's essential to consider other factors and conduct a comprehensive assessment, as hemoglobinopathies can have various presentations, and additional tests may be needed for a definitive diagnosis. I hope this answers your question. Do not hesitate to ask again, if there is still any doubt

It's my pleasure

If the palindrome is relatively short and is located in a single-stranded region of the DNA, it might form a hairpin structure. In a hairpin structure, the single-stranded region folds back on itself, creating a loop and a stem. if the palindrome is part of a double-stranded region of DNA, it may contribute to the formation of a cruciform structure. I hope this answers your question. If not, don't hesitate to ask again

@@learnbiotechnologyandmicrobiol Yes sir, thankyou!!

Most welcome 🤗🤗🤗

Thankyou

Because it is caused by a virus

3rd image is same done is viral pharyngitis

You're very welcome!

You're so welcome!

Antibiotics will work fine and you will be good in days

Thankyou for your kind comments. Keep watching. I'll soon start lectures in Hindi

@@learnbiotechnologyandmicrobiol Sir its fine in english, easy to grasp🙂

Interferon is an antiviral mechanism

I will make videos in Urdu in Sha Allah

The lysis buffer and solution are used for both gram positive and negative one but for gram positive you have to add lysozyme as an extra component because of the thick peptidoglycan later in gram positive bacteria. I hope this answers your question. Feel free to ask if you have any more questions

@@learnbiotechnologyandmicrobiol can I add lysozyme enzyme with lysis solution ? I mean at the same time can I add both before inoculation?

most welcome