Regulation Of Extracellular Matrix Assembly Pathway Bioinformatics
Disease and disorder research has been conducted in relation to the Regulation Of Extracellular Matrix Assembly Pathway and Neoplasms, Pathologic Neovascularization. The study of the Regulation Of Extracellular Matrix Assembly Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Regulation Of Extracellular Matrix Assembly Pathway has been researched in relation to Extracellular Matrix Assembly, Fertilization, Cell Growth, Pathogenesis. The Regulation Of Extracellular Matrix Assembly Pathway complements our catalog of research reagents including antibodies and ELISA kits against SPARC, TNFRSF10B, FST.
Top Research Reagents
We have 826 products for the study of the Regulation Of Extracellular Matrix Assembly Pathway that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![N/A Follistatin [HRP]](https://images.novusbio.com/fullsize2/DATA_Follistatin_DFN00_ELISA_681.jpg)
![N/A Follistatin [HRP]](https://images.novusbio.com/fullsize2/DATA_Follistatin_DFN00_ELISA_682.jpg)
![Western Blot: TRAILR2/TNFRSF10B Antibody [NB100-56618] - TRAIL R2/TNFRSF10B Antibody [NB100-56618] - Total protein from HL-60, HepG2, HCT-116 and human placenta was separated on a 12% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2.0 ug/ml anti-TRAIL R2 in 1% non-fat milk in TBST and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.](https://images.novusbio.com/fullsize/TRAIL-R2-TNFRSF10B-Antibody-Western-Blot-NB100-56618-img0005.jpg)
![Immunohistochemistry-Paraffin: TRAILR2/TNFRSF10B Antibody [NB100-56618] - TRAIL R2/TNFRSF10B Antibody [NB100-56618] - Analysis of a formalin fixed paraffin-embedded (FFPE) human brain cerebellum using 1:200 conc. of TRAIL R2/TNFRSF10B antibody on a Bond Rx autostainer (Leica Biosystems). The assay involved 30 minutes of heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 9.0) and endogenous peroxidase quenching with peroxide block. The sections were incubated with primary antibody for 15 minutes and Bond Polymer Refine Detection (Leica Biosystems) with DAB was used for signal development followed by counterstaining with hematoxylin. Cytoplasmic staining was observed in the Purkinje cell layer.](https://images.novusbio.com/fullsize/TRAIL-R2-TNFRSF10B-Antibody-Immunohistochemistry-Paraffin-NB100-56618-img0007.jpg)
