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  • Book
    edited by Biji T. Kurien, R. Hal Scofield.
    Contents:
    Western blotting : origin and ascent of the species / W. Neal Burnette
    Methods to concentrate proteins for protein isolation, proteomic, and peptidomic evaluation / J. P. Dean Goldring
    Measuring protein concentration on nitrocellulose and after the electrophoretic transfer of protein to nitrocellulose / J. P. Dean Goldring
    Detection of blotted proteins : not all blockers are created equal / Vishal Kothari and Suresh T. Mathews
    Protein stains to detect antigen on membranes / Anil Dsouza and R. Hal Scofield
    Fluorescent labeling of proteins and its application to SDS-PAGE and Western blotting / F. Javier Alba, Salvador Bartolomé, Antonio Bermúdez, and Joan-Ramon Daban
    Rapid, antibody-free detection of recombinant proteins on blots using enzyme fragment complementation / Neil W. Charter, Joe Horecka Chin-Yee Loh, Albert Doan, Tom Wehrman, and Keith R. Olson
    Use of nonradioactive detection method for north and South-Western blot / Claudia Franke, Daniel Gräfe, Holger Bartsch, and Michael P. Bachmann
    Immunoblotting using radiolabeled reagents for detection / Holger Bartsch, Claudia Franke, and Michael P. Bachmann
    Immunoblotting of antigens : whole, strip, and new-line nitrocellulose membrane immunoblotting using the chemiluminescence technique / Yaser Dorri
    Detection of protein carbonyls by means of biotin hydrazide-streptavidin affinity methods / Kenneth Hensley
    Direct immunodetection of antigens within the precast polyacrylamide gel / Surbhi Desai, Boguslawa R. Dworecki, and Marie C. Nlend
    Quantitative analysis of signal transduction with in-cell Western immunofluorescence assays / Vince Boveia and Amy Schutz-Geschwender
    Ultrasensitive protein detection on dot blots and Western blots with semiconducting polymer dots / Fangmao Ye, Polina B. Smith, and Daniel T. Chiu
    Co-detection of target and total protein by CyDye labeling and fluorescent ECL plex immunoblotting in a standard proteomics workflow / Caitriona Scaife, Ciara A. McManus, Pamela M. Donoghue, and Michael J. Dunn
    Using biotinylated proteins to demonstrate immunodetection of antigens via Western blotting, dot blots, and immunohistochemistry / Thomas Millar, Ronald Knighton, and Jo-Anne Chuck
    Calcium binding by Ro 60 multiple antigenic peptides on PVDF membrane / Biji T. Kurien and Michael P. Bachmann
    Sequential use of immunoblots for characterization of autoantibody specificities / Holger Bartsch and Michael P. Bachmann
    Nanogold immunodetection detection systems for the identification of autoantigens by Western blotting / Jacen S. Moore and R. Hal Scofield
    Application of intermittent microwave irradiation to Western blot analysis / Yu-Ting Liu and Shinya Toyokuni
    Visualization of unstained protein bands on PVDF / Jun Park, Masaharu Mabuchi, and Ajay Sharma
    Multiplexed fluorescent immunodetection using low autofluorescence Immobilon®-FL membrane / Jun Park, Masaharu Mabuchi, and Ajay Sharma
    Cold microwave-enabled protein detection and quantification / Niels Grützner, Romy M. Heilmann, Aaron G. Smith, Carol B. Johnson, Stanislav Vitha, Jörg M. Steiner, and Andreas K. Holzenburg
    TLC-blot (Far-Eastern blot) and its application to functional lipidomics / Takao Taki
    Analysis of electroblotted proteins by mass spectrometry / Jose L. Luque-Garcia and Thomas A. Neubert
    On-membrane renaturation of recombinant Ro60 autoantigen by calcium ions / Biji T. Kurien and Michael P. Bachmann
    Phosphoprotein detection on protein electroblot using a phosphate-specific fluorophore / Lee Broderick Bockus and R. Hal Scofield
    Purification of tryptic digests on polyvinylidene difluoride membrane / Biji T. Kurien and R. Hal Scofield
    Detection of blotted proteins on nitrocellulose/PVDF membranes by Alta / Jayanta K. Pal, Shilpa J. Rao, and Dhanashri J. Godbole
    Nonstripping "rainbow" and multiple antigen detection (MAD) Western blotting / Stan (Stanislaw) Krajewski, Michelle M. Tsukamoto, Xianshu Huang, and Sebastian B. Krajewski
    Supported molecular matrix electrophoresis / Yu-ki Matsuno and Akihiko Kameyama
    Parafilm-M®, an available cost-effective alternative for immuno-blot pouches / Syed M. S. Quadri
    Succinylation-alcian blue staining of mucins on polyvinylidene difluoride membranes / Akihiko Kameyama, Weijie Dong, and Yu-ki Matsuno
    Comparison of chemiluminescence vs. infrared techniques for detection of fetuin-A in saliva / Suresh T. Mathews, Emily Graff, Robert L. Judd, and Vishal Kothari
    A novel methodology for stripping and reprobing of Western blots originally developed with colorimetric substrate TMB / Parmita Kar, Saurabh Kumar Agnihotri, Archana Sharma, Rekha Sachan, Madan Lal Bhatt, and Monika Sachdev
    Other notable methods of membrane protein detection : a brief review / Biji T. Kurien and R. Hal Scofield
    Nitrocellulose membrane : the new canvas / Jasmin R. Kurien and Bianca A. Kurien
    Invisible ink marking in ECL membrane assays / Biji T. Kurien.
    Digital Access Springer 2015
  • Book
    vstupitelʹnai͡a statʹi͡a S.V. Vinogradovoĭ ; bibliografii͡a sostavlena L.I͡A. Nilovoĭ, O.F. Rumi͡ant͡sevoĭ, i S.V. Semenovoĭ.
    Print 1982
  • Article
    Landrey SR, Applegate R, Cardenas JM.
    Comp Biochem Physiol B. 1978;60(4):383-8.
    1. Analysis of the enolase isozymic distribution has been performed in tissues of the Coho salmon, using electrophoretic separation on cellulose acetate strips followed by localization of enzymatic activity. 2. A total of six electrophoretically distinct forms are seen in Coho salmon in patterns that differ both qualitatively and quantitatively from one tissue to another. 3. The isozymes in skeletal muscle and liver are sufficiently similar to one another that a purification procedure previously developed for trout muscle enolase by Cory & Wold (1966) can be used to partially purify enolase from either of the above-mentioned Coho tissues. The main form of enolase in Coho muscle has an isoelectric point of 7.57. 4. Both liver and skeletal muscle enolases can be reversibly denatured in guanidine HCl and subsequently renatured. Liver enolase appeared to renature somewhat faster than muscle enolase under the same conditions. 5. While polyploidy among salmonids may contribute to the complexity of enolase patterns in fish, the differences in isozymic patterns seen from one tissue to another indicate the presence of distinct, nonallelic genes, probably arising through gene duplication.
    Digital Access Access Options