Lecturer, Good at teaching, impropmtu speaking, Good communication sk
Resume:
RESUME
UMASHANKAR B M
Mobile No: 799-***-****
Email id:
************@*****.***
Permanent Address :
#*, ************* *****, ************
(Res), Narasipura (P), Sompura (H),
Nelamangala (T),
Bangalore Rural District
Pin Code – 562111.
Personal Data:
Father Name: Mallikarjunaiah D M
Date Of Birth: 16th June 1993
Sex : Male
Nationality : Indian
Marital Status: Single
Languages Known:
Kannada & English.
Experience:
Two months Experience in
B.Ed. Practice teaching class.
Experience in class seminar
during MSc.
Professional Objective
To work with a reputed institution as an teacher that will provide me a good platform to utilize my teaching and administration skills and will help me to grow my career.
Academics
Course College/School
Year of
Passing
Percentage
M.Sc.
(Biochemistry)
Kuvempu
university
Shankarghatta
Shivamooga
2018 67.77%
B.Ed.
(Physical
Science &
Biology )
Sree. Sarvajna
College Of
Education,
Vijayanagar,
Bangalore – 40.
2015 82.15%
B.Sc.
(CBZ)
Sree. Siddaganga
F.G.C. of Arts,
Science And
Commerce,
Tumkur.
2014 75.21%
P.U.C
Sree. Siddaganga
Boys PU
College,
BH Road,
Tumkur.
2011 48.33%
S.S.L.C
Sri.
Siddalingeshwara
Res H.R.SEC.
School,
Siddaganga,
Tumkur.
2009 80.16%
Academic project: Isolation and purification of Taq DNA polymerase enzyme This project is done for partial fulfilment requirement degree for M.sc in Biochemistry. It was done in Shreedhar Bhat’s laboratories Bangalore. Under the guidance of Dr.Shreedhar bhat. Director of Shreedhar bhat laboratories and co guided by Dr. Shivayoggeshwar Neelagund Professor Department of Biochemistry. PCR is a most widely-used technique in biology, which utilizes thermostable DNA polymerase from Thermus aquaticus (Taq).The gene that encoded the Taq DNA polymerase had been cloned and expressed in Escherichia coli efficiently. This has greatly facilitated the production and reduced the price of the enzyme. Even so the expense spent on the enzyme is also very great to some labs, for example some genetics labs which need to do a large number of PCRs to detect polymorphism of molecular markers. Thus, many labs made the enzyme by themselves to save money. The full-length Taq DNA polymerase (Taq Pol Ι) gene encodes a 94 kD native protein with 832 amino acids. Subsequently, a 61 kD Taq Pol Ι, termed ‘Stoffel fragment’ with 544 amino acids, was obtained. Comparing with the full-length Taq Pol Ι, the deletion version lost 5 to 3 exonuclease activity .This was usually extracted with pluthero’s method. In this method used ammonium sulphate to precipitate the enzyme. And this method used as partial purification for Taq DNA for complete purification column chromatography is used.
Interested area:
Teaching
Research and development in life science.
Professional qualifications:
Through understanding of the subject with ability to convey the same to the students.
Good communication and comprehension abilities.
Posse’s knowledge about the internal administrative tasks that are performed with in institutions.
Skilled in teaching students adopting lecturing method.
Expert in English keyboard Typing.
Preparing question paper based on blue print.
Evaluation the answer papers based on CCE method. EXTRA ACTIVITIES:
Participated in essay writing and quiz competitions at School & college levels.
Participated in cultural activities.
Skill Sets:
Anchoring
Impromptu Speech
Conflict resolution
Creative writing
Event management and Class room Management
Quick learning
Comfortable with computer (M.S. Office & Internet) Hobbies: Reading books, listening Music, Watching Drama & Movies. References: Dr. Shivayogeshwar Neelagund Msc, PhD, PGDCA and PDF in USA Professor Department of BIO CHEMISTRY
KUVEMPU UNIVERSITY Shivamogga
Email: neelgund @gmail.com, ********@*******.**.** Phone number- +91-944*******
DECLARATION
I hereby declare that all my above details are true and best to my knowledge. Date:
Place:
Yours faithfully,
(UMASHANKAR B M)
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