Abstract: A method for the determination and quantification of collagen types (I- V) using sample pretreatment has been developed. This work is a continuation of our previous work dealing with the determination of collagen types I and III in tissues [1]. The tissues (rat placenta and porcine cartilage) were firstly homogenized with a pestle in a grinding mortar with liquid ni-trogen. Collagens were isolated from these tissues by cleavage with pepsin. The collagen types of interest were then pre-cipitated successively by adding sodium chloride. For quantitation purposes, the sample preparation protocol has been simplified to the one-step precipitation of collagens from a solution containing 4.5 mol/L of sodium chloride. The frac-tions were f...
24 Annotation: This work is concerned with the development and application of high performance separ...
Sensitive and selective assay of collagen is of substantial importance to the diagnostic study of he...
Sequence analysis of bovine and porcine collagen type I indicates that some partial sequences are sp...
The methods of quantitating the relative amounts of type I and III collagens in samples containing c...
IntroductionThis study develops assays to quantify collagen subtypes and crosslinks with liquid chro...
The purpose of this study was to establish a collagen determination method based on an isotope-label...
With a view to facilitating the study of human genetic connective tissue diseases we have developed ...
Collagen is a ubiquitous biomaterial in vertebrate animals. Although each of its 28 subtypes contrib...
Collagen is one of the most ubiquitous proteins in the animal kingdom and the dominant protein in ex...
Abstract Collagens are the most abundant proteins in vertebrate tissues and constitute significant m...
We present a novel method for the isolation and analysis of the bone collagen (I) α2 chain carboxyte...
Collagens are the most abundant proteins in animals and are involved in many physiological/pathologi...
Collagen, which is one of the most abundant proteins in mammalian proteomes, is of significant medic...
SummaryType II collagen is an excellent indicator of the cartilage phenotype. Accurate quantificatio...
Abstract Fibrillar type I and III collagens are the major constituents of the extracellular matrix, ...
24 Annotation: This work is concerned with the development and application of high performance separ...
Sensitive and selective assay of collagen is of substantial importance to the diagnostic study of he...
Sequence analysis of bovine and porcine collagen type I indicates that some partial sequences are sp...
The methods of quantitating the relative amounts of type I and III collagens in samples containing c...
IntroductionThis study develops assays to quantify collagen subtypes and crosslinks with liquid chro...
The purpose of this study was to establish a collagen determination method based on an isotope-label...
With a view to facilitating the study of human genetic connective tissue diseases we have developed ...
Collagen is a ubiquitous biomaterial in vertebrate animals. Although each of its 28 subtypes contrib...
Collagen is one of the most ubiquitous proteins in the animal kingdom and the dominant protein in ex...
Abstract Collagens are the most abundant proteins in vertebrate tissues and constitute significant m...
We present a novel method for the isolation and analysis of the bone collagen (I) α2 chain carboxyte...
Collagens are the most abundant proteins in animals and are involved in many physiological/pathologi...
Collagen, which is one of the most abundant proteins in mammalian proteomes, is of significant medic...
SummaryType II collagen is an excellent indicator of the cartilage phenotype. Accurate quantificatio...
Abstract Fibrillar type I and III collagens are the major constituents of the extracellular matrix, ...
24 Annotation: This work is concerned with the development and application of high performance separ...
Sensitive and selective assay of collagen is of substantial importance to the diagnostic study of he...
Sequence analysis of bovine and porcine collagen type I indicates that some partial sequences are sp...