Decorin Antibody Rabbit Monoclonal / DCN [clone DCN/8760R] (V4308)

Decorin Antibody Rabbit Monoclonal Prostate IHC. Immunohistochemistry of Decorin antibody in human prostate carcinoma tissue. Formalin-fixed, paraffin-embedded human prostate carcinoma was stained using rabbit monoclonal Decorin antibody (clone DCN/8760R). Heat induced epitope retrieval was performed by boiling tissue sections in 10mM Tris with 1mM EDTA, pH 9, for 20 min followed by cooling prior to staining. HRP-DAB brown chromogenic signal highlights extracellular stromal connective tissue and desmoplastic matrix surrounding malignant glands, consistent with Decorin localization within collagen-rich tumor stroma.

SDS-PAGE analysis of purified, BSA-free Decorin antibody rabbit monoclonal (clone DCN/8760R) as confirmation of integrity and purity.

Decorin Antibody Human Tissue Panel WB. Western blot analysis of human 1) heart, 2) lung, and 3) skeletal muscle tissue lysates using Decorin Antibody (clone DCN/8760R) detects multiple bands between approximately 50-120 kDa, consistent with glycosylated and partially processed forms of Decorin (DCN). The higher molecular weight bands reflect glycosaminoglycan-modified Decorin, while lower bands likely represent core protein or proteolytic fragments. The consistent banding pattern across tissues supports reliable detection of DCN and its post-translationally modified variants in extracellular matrix-rich samples.

Decorin Antibody Multi-Species Heart and Lung WB. Western blot analysis of heart and lung tissue lysates from human, mouse, rat, hamster, guinea pig, and rabbit using Decorin Antibody (clone DCN/8760R) detects multiple bands ranging from approximately 50-120 kDa, consistent with glycosylated and partially processed forms of Decorin (DCN). The higher molecular weight bands reflect glycosaminoglycan-modified Decorin, while lower bands likely represent core protein or proteolytically processed forms. The conserved banding pattern across species supports reliable detection of DCN and its post-translationally modified variants in extracellular matrix-rich tissues.