Literature DB >> 7105651

Precision method to determine denaturation temperature of collagen using ultraviolet difference spectroscopy.

C C Danielsen.   

Abstract

Ultraviolet difference spectroscopy was used to measure the thermal stability of molecular collagen under nonequilibrium conditions. A method using equipment commonly found in many laboratories and procedures for data gathering and data treatment are described. The melting temperature (Tm) was determined with high precision (S.D.: 0.10 degrees C) by means of close thermal spacing of recorded datas. Application of curve fitting procedures on the denaturation data enhanced the recognition of details in the thermal transition. Small transitions could be discriminated and thermally located with an accuracy of +/- 0.3 degrees C.

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Year:  1982        PMID: 7105651     DOI: 10.1016/s0174-173x(82)80030-7

Source DB:  PubMed          Journal:  Coll Relat Res        ISSN: 0174-173X


  3 in total

1.  Thermal stability of human-fibroblast-collagenase-cleavage products of type-I and type-III collagens.

Authors:  C C Danielsen
Journal:  Biochem J       Date:  1987-11-01       Impact factor: 3.857

2.  Reconstituted collagen fibrils. Fibrillar and molecular stability of the collagen upon maturation in vitro.

Authors:  C C Danielsen
Journal:  Biochem J       Date:  1984-09-15       Impact factor: 3.857

3.  Age-related thermal stability and susceptibility to proteolysis of rat bone collagen.

Authors:  C C Danielsen
Journal:  Biochem J       Date:  1990-12-15       Impact factor: 3.857

  3 in total

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