Exosome Research - Starting Package Reference: EX11 The pack has been designed to introduce you to our complete range of solutions from isolation to the detection of exosomes in a wide range of applications. This pack is intended both for researchers who are new to the field and existing researchers who would like to try our kit to compare to methods they currently use.
Trident 10X TBST Reference: GTX30976 This buffer is supplied as 10X TBS solution containing 1% Tween. It is used as 1X in all western blotting, ELISA and Chemiluminescence assays as a washing buffer, making blocking solution, diluting HRP-secondary and primary antibody etc. This buffer does not contain any phosphate, sodium azide or mercury preservative and can be used for dilution of all antibodies, including peroxidase, and antibodies to phosphoproteins. This buffer does not contain any proteins.
Trident 10X PBST Reference: GTX30977 This buffer is supplied as 10X PBS solution containing 1% Tween. It is used as 1X in all western blotting, ELISA and Chemiluminescence assays as a washing buffer, making blocking solution, diluting HRP-secondary and primary antibody etc. This buffer does not contain any sodium azide or mercury preservative and can be used for dilution of all antibodies, including peroxidase. This buffer does not contain any proteins.
Citrate buffer, 10X pH6.0 Reference: GTX30936 This buffer is intended for heat-induced epitope retrieval (HIER) of formalin-fixed paraffin-embedded (FFPE) tissue sections prior to application of antibodies. In IHC, commonly used fixatives (like formalin) mask tissue antigens through cross-linking, often resulting in poor or no staining. The use of this buffer on FFPE tissue sections improves antibody accessibility to tissue antigens.
EDTA buffer, 10X pH 8.0 Reference: GTX30937 This buffer is intended for heat-induced antigen retriever on formalin-fixed paraffin-embedded (FFPE) tissue sections prior to application of antibodies. In IHC most commonly used fixative like formalin mask tissue antigens (cellular, membrane and nuclear) by cross-linking process, this results in poor or no staining in IHC. The use of this buffer on FFPE tissue section improves accessibility of antibodies to tissue antigens.