Category: probe

buffer protein, Free Radical Generation in Far-UV Synchrotron Radiation Circular Dichroism Assays-Protein and Buffer Composition Contribution

Free Radical Generation in Far-UV Synchrotron Radiation Circular Dichroism Assays-Protein and Buffer Composition ContributionFree Radical Generation in Far-UV Synchrotron Radiation Circular Dichroism Assays-Protein and Buffer Composition Contribution

A great tool to investigate the ligands and/or environmental contribution to protein stability is represented by the Synchrotron Radiation Round Dichroism UV-denaturation assay that consists within the acquisition of a

immunoblotting technique, Completing the Immunological Fingerprint by Refractory Proteins: Autoantibody Screening via an Improved Immunoblotting Technique.

Completing the Immunological Fingerprint by Refractory Proteins: Autoantibody Screening via an Improved Immunoblotting Technique.Completing the Immunological Fingerprint by Refractory Proteins: Autoantibody Screening via an Improved Immunoblotting Technique.

Figuring out autoantigens of serological autoantibodies requires costly strategies, reminiscent of protein microarrays or IP+MS. Thus, sera are generally pre-screened for attention-grabbing immunopatterns by way of immunocytochemistry/immunohistochemistry. Nonetheless, distinguishing immunopatterns

acid phosphatase assay, Smartphone colorimetric assay of acid phosphatase based on a controlled iodine-mediated etching of gold nanorods

Smartphone colorimetric assay of acid phosphatase based on a controlled iodine-mediated etching of gold nanorodsSmartphone colorimetric assay of acid phosphatase based on a controlled iodine-mediated etching of gold nanorods

A easy however environment friendly colorimetric assay was developed for the detection and quantification of acid phosphatase (ACP) utilizing a smartphone. This technique relies on target-controlled iodine-mediated etching of gold