DEPARTMENT OF MICROBIOLOGY University of Delhi South campus New Delhi-110021 PhD Course work
... regulation, Utilization of other modes of nitrogen, nitrate and nitrite utilization, amino acid biosynthetic pathways and their regulation, amino acid utilization – reduction amination and deamination; decarboxylation; Stickland reaction; amino acid oxidases, polyamine biosynthesis and utilization L ...
... regulation, Utilization of other modes of nitrogen, nitrate and nitrite utilization, amino acid biosynthetic pathways and their regulation, amino acid utilization – reduction amination and deamination; decarboxylation; Stickland reaction; amino acid oxidases, polyamine biosynthesis and utilization L ...
Nucleosides, nucleotides, nucleic acids
... protein synthesis. Single stranded. - ribosomal RNA = rRNA : components of the ribosome, which is the site of protein synthesis (translation). rRNA forms self-complementary double-stranded regions (in RNA there is Uracil instead of Thymine as a base, it forms double hydrogen bonds with Adenine). - t ...
... protein synthesis. Single stranded. - ribosomal RNA = rRNA : components of the ribosome, which is the site of protein synthesis (translation). rRNA forms self-complementary double-stranded regions (in RNA there is Uracil instead of Thymine as a base, it forms double hydrogen bonds with Adenine). - t ...
Executive Summary - Defra Science Search
... 18. The second method of generating arrays was Suppression Subtractive Hybridisation. This produces cDNA libraries that are greatly enriched for genes with altered gene expression consequent on exposure to a hazardous chemical. Individual genes can be isolated from such libraries and identified by s ...
... 18. The second method of generating arrays was Suppression Subtractive Hybridisation. This produces cDNA libraries that are greatly enriched for genes with altered gene expression consequent on exposure to a hazardous chemical. Individual genes can be isolated from such libraries and identified by s ...
File
... Eukaryotic cells modify mRNA after transcription. Splicing of mRNA increases the number of different proteins an organism can produce. Gene expression is regulated by proteins that bind to specific base sequences in DNA. The environment of a cell and of an organism has an impact on gene expression. ...
... Eukaryotic cells modify mRNA after transcription. Splicing of mRNA increases the number of different proteins an organism can produce. Gene expression is regulated by proteins that bind to specific base sequences in DNA. The environment of a cell and of an organism has an impact on gene expression. ...
What_I_need_to_know_about_Protein_Synthesis_2013
... 20. Protein synthesis is the process of making _________ A gene is the instructions to make a _____________ The protein is the expressed __________ of the organism. 21. Where does protein synthesis occur in the cell? _________________ 22. The process of protein synthesis begins with one ____________ ...
... 20. Protein synthesis is the process of making _________ A gene is the instructions to make a _____________ The protein is the expressed __________ of the organism. 21. Where does protein synthesis occur in the cell? _________________ 22. The process of protein synthesis begins with one ____________ ...
Learning objectives
... 12. Describe the process of nucleic acid hybridization. 13. Describe the Southern blotting procedure and explain how it can be used to identify the heterozygous carriers of a mutant allele. 14. Explain how Northern blotting or the reverse transcriptase-polymerase chain reaction (RT-PCR) can be used ...
... 12. Describe the process of nucleic acid hybridization. 13. Describe the Southern blotting procedure and explain how it can be used to identify the heterozygous carriers of a mutant allele. 14. Explain how Northern blotting or the reverse transcriptase-polymerase chain reaction (RT-PCR) can be used ...
Learning objectives
... 12. Describe the process of nucleic acid hybridization. 13. Describe the Southern blotting procedure and explain how it can be used to identify the heterozygous carriers of a mutant allele. 14. Explain how Northern blotting or the reverse transcriptase-polymerase chain reaction (RT-PCR) can be used ...
... 12. Describe the process of nucleic acid hybridization. 13. Describe the Southern blotting procedure and explain how it can be used to identify the heterozygous carriers of a mutant allele. 14. Explain how Northern blotting or the reverse transcriptase-polymerase chain reaction (RT-PCR) can be used ...
Chapter 16 and 17 Review
... The monomer of DNA is called _____________. What are the three parts that make up the DNA monomer? Name the four DNA nucleotides. How do the nucleotides pair? How many strands are in a DNA molecule? What kind of bond holds DNA strands together? The two DNA strands are said to be antiparallel. What d ...
... The monomer of DNA is called _____________. What are the three parts that make up the DNA monomer? Name the four DNA nucleotides. How do the nucleotides pair? How many strands are in a DNA molecule? What kind of bond holds DNA strands together? The two DNA strands are said to be antiparallel. What d ...
STUDY GUIDE SEMESTER 2 EXAM 4 Dr. Marks Name: Class
... Refer to the illustration above. The anticodons for the codons in the mRNA with the sequence CUCAAGUGCUUC are ...
... Refer to the illustration above. The anticodons for the codons in the mRNA with the sequence CUCAAGUGCUUC are ...
Genetic Improvement of Crop Plants short version with animation links
... • Crops, strains and genes have moved around the globe. ...
... • Crops, strains and genes have moved around the globe. ...
Course Outline
... To enable understanding of the principles of human nutrition and knowing the types and amounts of macronutrients that are needed to maintain optimal health. 4. To give students information about the structure and function and the clinical importance of fat-soluble vitamins in health and disease. 5. ...
... To enable understanding of the principles of human nutrition and knowing the types and amounts of macronutrients that are needed to maintain optimal health. 4. To give students information about the structure and function and the clinical importance of fat-soluble vitamins in health and disease. 5. ...
Ch 8 Genetic Technology and Diagnostics
... •Primers: DNA strands 15 – 30 bases long that serve as landmarks where DNA amplification should begin •DNA polymerase from thermophilic bacteria - “Taq” polymerase isolated from Thermus aquaticus - remain active at elevated temperatures used in PCR •Thermal cycler: automatically performs the cyclic ...
... •Primers: DNA strands 15 – 30 bases long that serve as landmarks where DNA amplification should begin •DNA polymerase from thermophilic bacteria - “Taq” polymerase isolated from Thermus aquaticus - remain active at elevated temperatures used in PCR •Thermal cycler: automatically performs the cyclic ...
1 - marric.us
... 30. What is the function of each of the following organelles? a. Cell membrane (pg 187) d. Ribosomes (pg 193) b. Endoplasmic Reticulum (pg 194) e. Chloroplasts (pg 197) c. Golgi apparatus (pg 195) 31. What are the differences between a prokaryotic and eukaryotic cell? (pg 185-186) 32. Make a sketch ...
... 30. What is the function of each of the following organelles? a. Cell membrane (pg 187) d. Ribosomes (pg 193) b. Endoplasmic Reticulum (pg 194) e. Chloroplasts (pg 197) c. Golgi apparatus (pg 195) 31. What are the differences between a prokaryotic and eukaryotic cell? (pg 185-186) 32. Make a sketch ...
Class: AP Bio Unit: Genetics Estimated Date Target Reading
... require use of the rule of multiplication and two probability questions that require use of the rule of addition.) Describe non-mendelian inheritance and human genetic disorders. ...
... require use of the rule of multiplication and two probability questions that require use of the rule of addition.) Describe non-mendelian inheritance and human genetic disorders. ...
Real-time polymerase chain reaction
A real-time polymerase chain reaction is a laboratory technique of molecular biology based on the polymerase chain reaction (PCR). It monitors the amplification of a targeted DNA molecule during the PCR, i.e. in real-time, and not at its end, as in conventional PCR. Real-time PCR can be used quantitatively (Quantitative real-time PCR), semi-quantitatively, i.e. above/below a certain amount of DNA molecules (Semi quantitative real-time PCR) or qualitatively (Qualitative real-time PCR).Two common methods for the detection of PCR products in real-time PCR are: (1) non-specific fluorescent dyes that intercalate with any double-stranded DNA, and (2) sequence-specific DNA probes consisting of oligonucleotides that are labelled with a fluorescent reporter which permits detection only after hybridization of the probe with its complementary sequence.The Minimum Information for Publication of Quantitative Real-Time PCR Experiments (MIQE) guidelines propose that the abbreviation qPCR be used for quantitative real-time PCR and that RT-qPCR be used for reverse transcription–qPCR [1]. The acronym ""RT-PCR"" commonly denotes reverse transcription polymerase chain reaction and not real-time PCR, but not all authors adhere to this convention.