Drafting Patent Claims for Filing in the United States
... (c) determining the amounts of [product] produced in the first and second reaction mixtures; and (d) comparing the amounts of [product] produced in the first and second reaction mixtures; wherein the chemical is capable of inhibiting X enzyme activity if the amount of [product] produced in the secon ...
... (c) determining the amounts of [product] produced in the first and second reaction mixtures; and (d) comparing the amounts of [product] produced in the first and second reaction mixtures; wherein the chemical is capable of inhibiting X enzyme activity if the amount of [product] produced in the secon ...
Document
... involved into formation of the whole organism body. •Motor proteins. These proteins can convert chemical energy into mechanical energy. actin and myosin are responsible for muscular motion. •Receptors These proteins are responsible for signal detection and translation into other type of signal. •Sig ...
... involved into formation of the whole organism body. •Motor proteins. These proteins can convert chemical energy into mechanical energy. actin and myosin are responsible for muscular motion. •Receptors These proteins are responsible for signal detection and translation into other type of signal. •Sig ...
D2 - Interchim
... can be extracted and purified from bacteriophages, bacteria, fungi and yeasts, plants, soil, tissues, food/feed, blood and cell cultures. An absolutely new feature of PrestoSpin D is the purification of plasmid DNA in midi format, cosmid and BAC DNA, using mini spin column purification. The PrestoSp ...
... can be extracted and purified from bacteriophages, bacteria, fungi and yeasts, plants, soil, tissues, food/feed, blood and cell cultures. An absolutely new feature of PrestoSpin D is the purification of plasmid DNA in midi format, cosmid and BAC DNA, using mini spin column purification. The PrestoSp ...
protocol: restriction endonuclease digestion/analysis of
... A single PCR-generated band in a gel does not always indicate a single amplification product. One way to quickly determine if there is more than one product is to digest the PCR product with restriction endonucleases. For example, following restriction endonuclease digestion, if DNA fragments are vi ...
... A single PCR-generated band in a gel does not always indicate a single amplification product. One way to quickly determine if there is more than one product is to digest the PCR product with restriction endonucleases. For example, following restriction endonuclease digestion, if DNA fragments are vi ...
Single-stranded DNA-binding Proteins
... The combination of electrostatic, hydrogen-bonding and stacking interactions from proteins to ssDNA forms the basis for ssDNA binding and specificity. Unfortunately, dsDNA, dsRNA and single-stranded RNA (ssRNA) share many of these properties. How does an ssDNA-binding protein exclude these competing ...
... The combination of electrostatic, hydrogen-bonding and stacking interactions from proteins to ssDNA forms the basis for ssDNA binding and specificity. Unfortunately, dsDNA, dsRNA and single-stranded RNA (ssRNA) share many of these properties. How does an ssDNA-binding protein exclude these competing ...
Tuning Biphenyl Dioxygenase for Extended Substrate Specificity
... bphA gene from Burkholderia cepacia LB400 and Pseudomonas pseudoalcaligenes KF707. Activities were calculated from three independent experiments. ...
... bphA gene from Burkholderia cepacia LB400 and Pseudomonas pseudoalcaligenes KF707. Activities were calculated from three independent experiments. ...
Genomic DNA Purification Protocol
... subtyping methods have been refined over the past few years to aid in epidemiological investigation of outbreaks. One method, fluorescence-based Amplified Fragment Length Polymorphism (fbAFLP) DNA fingerprinting, has become a valuable technique for characterizing bacterial strains (1–3). For a clini ...
... subtyping methods have been refined over the past few years to aid in epidemiological investigation of outbreaks. One method, fluorescence-based Amplified Fragment Length Polymorphism (fbAFLP) DNA fingerprinting, has become a valuable technique for characterizing bacterial strains (1–3). For a clini ...
Lab - Week One: The Scientific Method
... rectangular grey/purplish post-it note. (A table of polar and non-polar amino acids will be provided for each table). charging tRNAs with the correct amino acid, and aligning tRNA/amino acids where they would base pair with the mRNA transcript. c) Find the first AUG and place your ribosome above it. ...
... rectangular grey/purplish post-it note. (A table of polar and non-polar amino acids will be provided for each table). charging tRNAs with the correct amino acid, and aligning tRNA/amino acids where they would base pair with the mRNA transcript. c) Find the first AUG and place your ribosome above it. ...
Our work was originally motivated my collaboration with Drs
... the agents of interest. This library will be used to 'bio-pan' for phages that bind to a number of toxins and infectious agents and can, thus, provide an endless supply of low cost, reliable, specific, and stable artificial receptors. ...
... the agents of interest. This library will be used to 'bio-pan' for phages that bind to a number of toxins and infectious agents and can, thus, provide an endless supply of low cost, reliable, specific, and stable artificial receptors. ...
Recombinant DNA Technology
... nature more often than in the laboratory; – for example, every time a bacteria phage or eukaryotic virus infects its host cell and integrates its DNA into the host genome, a recombinant is created. – Occasionally, these viruses pick up a fragment of host DNA when they excise from their host’s genome ...
... nature more often than in the laboratory; – for example, every time a bacteria phage or eukaryotic virus infects its host cell and integrates its DNA into the host genome, a recombinant is created. – Occasionally, these viruses pick up a fragment of host DNA when they excise from their host’s genome ...
Contents Introduction Storage and Stability - Omega Bio-tek
... All components of the SQ Plant DNA Kit are stable for at least 12 months from date of purchase when stored at Room Temperature except Rnase A which should be stored at 2-8°C. During shipment, or storage in cool ambient conditions, precipitates may form in the some of the buffers. Dissolve such depos ...
... All components of the SQ Plant DNA Kit are stable for at least 12 months from date of purchase when stored at Room Temperature except Rnase A which should be stored at 2-8°C. During shipment, or storage in cool ambient conditions, precipitates may form in the some of the buffers. Dissolve such depos ...
PART I
... b) Suppression subtraction hybridization (SSH): It was developed a PCR-based strategy to clone differentially expressed gene transcripts. Although it is technically not an RT-PCR approach, it does require the synthesis of double-stranded DNA as a starting point for exponential PCR amplification of g ...
... b) Suppression subtraction hybridization (SSH): It was developed a PCR-based strategy to clone differentially expressed gene transcripts. Although it is technically not an RT-PCR approach, it does require the synthesis of double-stranded DNA as a starting point for exponential PCR amplification of g ...
Genomic DNA Extraction from Buccal Cells
... reaction without quantification. The normalized protocol provides DNA up to a concentration of 3 ng/μl, an ideal concentration for STR analysis. ...
... reaction without quantification. The normalized protocol provides DNA up to a concentration of 3 ng/μl, an ideal concentration for STR analysis. ...
DNA Replication and Recombination - HMartin
... to invert the physical but not biological direction of synthesis. ...
... to invert the physical but not biological direction of synthesis. ...
Section 11.2 Summary – pages 288
... (this is to make sure they are bringing the correct amino acidIf the anti-codon doesn’t base pair with the codon, then the wrong amino acid was brought) ...
... (this is to make sure they are bringing the correct amino acidIf the anti-codon doesn’t base pair with the codon, then the wrong amino acid was brought) ...
