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BIO315
BIO315

... functions in that they are both involved in transport within the cell, so they are similar. However, their functions are very distinct, & so are their sequences. ...
The phosphatidylinositol transfer protein RdgBβ binds 14-3
The phosphatidylinositol transfer protein RdgBβ binds 14-3

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Adenovirus-associated Virus Structural Protein Sequence Homology
Adenovirus-associated Virus Structural Protein Sequence Homology

... serum albumin as the standard protein. Radioiodination of virion protein. Purified virions were disrupted by treatment in I.O~o SDS at loo °C for 2 min. Samples containing 3o to 5o/zg of virus protein were suspended in 5o/zl of o'o5 M-phosphate buffer, pH 7'4 (buffer I), and the proteins iodinated b ...
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... and temperature, each protein folds spontaneously into one three-dimensional conformation, called the native conformation. 3.1.2 This conformation is usually thermodynamically the most stable (having the lowest Gibb’s free energy), and predominates among the innumerable theoretically possible ones. ...
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... or Tim8p–Tim13p is bound directly to the precursor. Equally plausible is a model in which the 70 kDa complexes form a link between the TOM and the TIM complexes. In this model, the precursor is not released into the intermembrane space but binds to the small Tim proteins as it emerges from the TOM c ...
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... 6. Dihazi, H., et al., One-step purification of recombinant yeast 6-phosphofructo-2-kinase after the identification of contaminants by MALDI-TOF MS. Protein Expr. Purif., 21(1), 201-209 (2001). 7. Fernandes, S., et al., Affinity extraction of dye- and metal ion-binding proteins in polyvinylpyrrolido ...
use of tobacco plants as bioreactors for the production of human
use of tobacco plants as bioreactors for the production of human

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embj201490361-sup-0002

... the accuracy of the intact measurement is typically better than 3 Da for a protein with a mass of 50K Da. B An expanded region of the mass spectrum focusing on the peak for TRIM5αrh. Note also the absence of species corresponding to unacetylated, demethionylated TRIM5α or methionylated TRIM5. ...
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... labeled by random primed DNA labeling using dioxigenin-dUTP as probe. Conditions of hydridization were: pre-hybridization 1 hr at 65ºC and hybridization o/n at 65ºC, in standard buffer: 5x SSC, 0.1% N-lauroylsarcosine, 0.02% SDS, 1% blocking reagent (#1096176 from Roche Applied Science) dissolved in ...
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Worksheet – Proteins Proteins are polymers of amino acids, joined

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Building Blocks of Life

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20. Biochemistry of Muscles and Connective Tissue

... •Structural unit of miofibril sarcomer •Both ends of thick miosin filaments are free •One end of thin filaments is attached to Z-plate ...
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Western blot



The western blot (sometimes called the protein immunoblot) is a widely used analytical technique used to detect specific proteins in a sample of tissue homogenate or extract. It uses gel electrophoresis to separate native proteins by 3-D structure or denatured proteins by the length of the polypeptide. The proteins are then transferred to a membrane (typically nitrocellulose or PVDF), where they are stained with antibodies specific to the target protein. The gel electrophoresis step is included in western blot analysis to resolve the issue of the cross-reactivity of antibodies.There are many reagent companies that specialize in providing antibodies (both monoclonal and polyclonal antibodies) against tens of thousands of different proteins. Commercial antibodies can be expensive, although the unbound antibody can be reused between experiments. This method is used in the fields of molecular biology, immunogenetics and other molecular biology disciplines. A number of search engines, such as CiteAb, Antibodypedia, and SeekProducts, are available that can help researchers find suitable antibodies for use in western blotting.Other related techniques include dot blot analysis, immunohistochemistry and immunocytochemistry where antibodies are used to detect proteins in tissues and cells by immunostaining, and enzyme-linked immunosorbent assay (ELISA).The method originated in the laboratory of Harry Towbin at the Friedrich Miescher Institute. The name western blot was given to the technique by W. Neal Burnette and is a play on the name Southern blot, a technique for DNA detection developed earlier by Edwin Southern. Detection of RNA is termed northern blot and was developed by George Stark at Stanford.
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