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F9550 - Datasheet - Sigma
F9550 - Datasheet - Sigma

... Stop reactions by the addition 5 µl stop solution. Boil for 5 min. at 95 °C. Load 4 µl sample on the denaturing gel. Note: wash the wells before loading. Run the mini gel at 200V with circulating cold water (~10°C) to reduce heating until the stain front reaches 1-2 cm of the bottom of the gel (brom ...
Nucleotide Metabolism -Biosynthesis- Dr. Sooad Al
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... Denovo Purine Nucleotide Biosynthesis  The two parent purine nucleotides of nucleic acids are adenosine 5monophosphate (AMP) and guanosine 5-monophosphate (GMP).  The origin of the carbon and nitrogen atoms of the purine ring system, as determined by John Buchanan using isotopic tracer experiment ...
A novel dipeptidomimetic containing a cyclic threonine.
A novel dipeptidomimetic containing a cyclic threonine.

... properties when compared to the natural analogs. For instance, these compounds contain an additional a-substituent which result in a tertiary a-carbon like in 1-amino-2-hydroxycyclohexane carboxylic acid derivatives.17–20 Apart from this, Thr has been used for the assembly of several cyclic systems ...
Vitamins Clinical relevance: homocystinuria: B6 and/or B12 and/or
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C485 Exam I
C485 Exam I

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A Supramolecular Peptide Synthesizer
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26.3 Synthesis of Amino Acids
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Discovery-4 - Peptide Machines, Inc.
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Multiple Choice Questions- Chemistry and Metabolism of nucleotides
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... increased levels of serum uric acid. These symptoms are characteristic of Lesch Nyhan syndrome, which is due to defectivea) Salvage pathway for pyrimidine biosynthesis b) Denovo synthesis of pyrimidines c) Xanthine oxidase d) HGPRT (Hypoxanthine Guanine Phospho Ribosyl Transferase) e) Formyl transfe ...
IOSR Journal of Applied Chemistry (IOSR-JAC)
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... 2278-5736. Volume 7, Issue 10 Ver. I. (Oct. 2014), PP 01-05. In continuation of this research another novel βLactam derivative amino acid was synthesized. NEPA-NCA (III) i.e. [(S)-ethyl-2-((S)-4-methyl-2,5-dioxooxazolidin-3-yl)-4-phenyl butanoate], is an important side chain component used in the sy ...
Sample exam
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Pa I I, hl.  L.   Blasticidin-S: on... Cycloheximide  has been used widely  as  ...
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... with blosticidin-S giver significant inhibition of incorporation into protein. incubation with 5Opg/ml blarticidin-S monohydrochloride giver almost complete inhibition of incorporation. is ...
Pentose Phosphate Pathway (aka Hexose monophosphate shunt)
Pentose Phosphate Pathway (aka Hexose monophosphate shunt)

... • G6PD is the most regulated enzyme: inhibition by NADPH, expression is dependent on insulin thus it is only expressed at high glucose concentration • Since the non-oxidative pathway is reversible, the direction is dependent on the need of the cell for ATP / acetyl CoA (energy / fatty acid synthesis ...
Document
Document

... • Look at the slides that follow containing the list of reactions on which to focus. • Re-read the indicated pages where each reaction is described in Creighton. Look at related power point slides and examples discussed in class. • Put together a summary sheet with each reaction in as much detail as ...
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Oligonucleotide synthesis



Oligonucleotide synthesis is the chemical synthesis of relatively short fragments of nucleic acids with defined chemical structure (sequence). The technique is extremely useful in current laboratory practice because it provides a rapid and inexpensive access to custom-made oligonucleotides of the desired sequence. Whereas enzymes synthesize DNA and RNA only in a 5' to 3' direction, chemical oligonucleotide synthesis does not suffer from this limitation, although it is, most often, carried out in the opposite, 3' to 5' direction. Currently, the process is implemented as solid-phase synthesis using phosphoramidite method and phosphoramidite building blocks derived from protected 2'-deoxynucleosides (dA, dC, dG, and T), ribonucleosides (A, C, G, and U), or chemically modified nucleosides, e.g. LNA, BNA.To obtain the desired oligonucleotide, the building blocks are sequentially coupled to the growing oligonucleotide chain in the order required by the sequence of the product (see Synthetic cycle below). The process has been fully automated since the late 1970s. Upon the completion of the chain assembly, the product is released from the solid phase to solution, deprotected, and collected. The occurrence of side reactions sets practical limits for the length of synthetic oligonucleotides (up to about 200 nucleotide residues) because the number of errors accumulates with the length of the oligonucleotide being synthesized. Products are often isolated by high-performance liquid chromatography (HPLC) to obtain the desired oligonucleotides in high purity. Typically, synthetic oligonucleotides are single-stranded DNA or RNA molecules around 15–25 bases in length.Oligonucleotides find a variety of applications in molecular biology and medicine. They are most commonly used as antisense oligonucleotides, small interfering RNA, primers for DNA sequencing and amplification, probes for detecting complementary DNA or RNA via molecular hybridization, tools for the targeted introduction of mutations and restriction sites, and for the synthesis of artificial genes.
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