Literature DB >> 8660517

Calibrating gelatin zymograms with human gelatinase standards.

G S Makowski1, M L Ramsby.   

Abstract

We describe the use of gelatinase standards from human capillary whole blood for calibrating gelatin zymograms. Capillary blood was obtained by fingerstick puncture and prepared in nonreducing Laemmli SDS-PAGE sample buffer without heating. Gelatin zymography revealed that whole blood (0.25- 1 microliter) contained substantial fibroblast-derived (72-kDa) and neutrophil-derived (92-, 130-, and 225-kDa) gelatinases which could be used for calibration purposes. Calibration was linear under different electrophoretic conditions using 6.5-10% polyacrylamide gels containing 1-2 mg/ml gelatin (correlation range, r = 0.990-0.998; perfect correlation, r = 1.000). The use of the standards for characterizing gelatinases from arthritic joint fluid is demonstrated. The standards are easily obtained and well characterized, and should facilitate interlaboratory comparison and standardization.

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Year:  1996        PMID: 8660517     DOI: 10.1006/abio.1996.0179

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  21 in total

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4.  Regulation of tissue-degrading factors and in vitro invasiveness in progression of breast cancer cells.

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5.  Interaction of amorphous calcium phosphate with fibrin in vitro causes decreased fibrinolysis and altered protease profiles: implications for atherosclerotic disease.

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6.  Binding of latent matrix metalloproteinase 9 to fibrin: activation via a plasmin-dependent pathway.

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Journal:  Inflammation       Date:  1998-06       Impact factor: 4.092

7.  Comparison of morphology, viability, and function between blood and milk neutrophils from peak lactating goats.

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8.  Binding of matrix metalloproteinase 9 to fibrin is mediated by amorphous calcium-phosphate.

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Journal:  Inflammation       Date:  1998-12       Impact factor: 4.092

9.  Antiangiogenic activity of orally absorbable heparin derivative in different types of cancer cells.

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10.  Matrix metalloproteinase-2-deficient fibroblasts exhibit an alteration in the fibrotic response to connective tissue growth factor/CCN2 because of an increase in the levels of endogenous fibronectin.

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