Kanako Iha

ORCID: 0000-0003-4292-0318
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About
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Research Areas
  • Biosensors and Analytical Detection
  • Advanced Biosensing Techniques and Applications
  • Extracellular vesicles in disease
  • Anodic Oxide Films and Nanostructures
  • Advanced biosensing and bioanalysis techniques
  • Genetics, Bioinformatics, and Biomedical Research
  • Peptidase Inhibition and Analysis
  • Virus-based gene therapy research
  • SARS-CoV-2 detection and testing
  • RNA Interference and Gene Delivery
  • Studies on Chitinases and Chitosanases
  • HIV-related health complications and treatments
  • Thermal properties of materials
  • Antimicrobial Peptides and Activities
  • Molecular Biology Techniques and Applications

Waseda University
2019-2023

Exosomes transfer molecules horizontally to surrounding cells and therefore have a key role in cancer progression. To clarify the of exosomes progression, trace amounts proteins their lumen membrane fractions should be analyzed separately. For this purpose, an adequate easy-to-use method separating must developed. Further, because contain only proteins, ultrasensitive protein detection is necessary. develop fraction separation method, we applied commercially available kit originally...

10.1016/j.ab.2022.114831 article EN cc-by Analytical Biochemistry 2022-07-31

Cancer cells communicate with each other via exosomes in the tumor microenvironment. However, measuring trace amounts of proteins is difficult, and thus cancer stemness-promoting mechanisms exosomal have not been elucidated. In present study, we attempted to quantify 78-kDa glucose-regulated protein (GRP78), which involved progression, released from cultured gastric using an ultrasensitive ELISA combined thio-NAD cycling. We also evaluated effects by application high-GRP78-containing cells....

10.3390/cancers14163887 article EN Cancers 2022-08-11

For the diagnosis of disease, ability to quantitatively detect trace amounts causal proteins from bacteria/viruses as biomarkers in patient specimens is highly desirable. Here we introduce a simple, rapid, and colorimetric assay de novo, ultrasensitive detection method. This consists sandwich enzyme-linked immunosorbent (ELISA) thionicotinamide-adenine dinucleotide (thio-NAD) cycling, forming an ELISA, which signal substrate (i.e., thio-NADH) accumulates triangular manner, accumulated...

10.20944/preprints201905.0328.v1 preprint EN 2019-05-28

An enzyme immunoassay, in which an (e.g., alkaline phosphatase, ALP) is conjugated with antibody, a precise and simple protein detection method. Precise measurements of enzymes at low concentrations allow for ultrasensitive detection. The application phosphorylated substrate to ALP, followed by using dephosphorylated thionicotinamide-adenine dinucleotide cycling, provides quantification ALP. We describe protocol detecting ALP the zeptomole level colorimetric

10.2116/analsci.21n009 article EN Analytical Sciences 2021-03-18

We used single-enzyme cycling with 3α-hydroxysteroid dehydrogenase (3α-HSD) [9].The 3α-HSD catalyzes the

10.33696/immunology.5.157 article EN cc-by Journal of Cellular Immunology 2023-03-23
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