IS-16 Innovation on Microfluidics-based Device for Single Cell Analysis, A Canine Cutaneous Mast Cell Tumor Model

Recently, our laboratory, Companion Animal Cancer Research Unit, CAC-RU is interested in cancer stem cell (CSC) analysis both at the single cell and the tissue-based levels. However, cellular heterogeneity is still the major hassle for our comprehension in CSC biology. Therefore, to overcome and eradicate this big obstacles, a single cell analysis method must be established. Our laboratory has finally setup and integrated the microfluidics-based single cell analysis into our CSC researches under the association with Department of Mechanical Engineering, Faculty of Engineering, Chulalongkorn University and Thai Micro-electronic Centre, NECTEC, Ministry of Science and Technology, Thailand and Faculty of Medical Technic, Mahidol University since 2013 till present

Developmental and tissue-specific expression of NITRs

Novel immune-type receptors (NITRs) are encoded by large multi-gene families and share structural and signaling similarities to mammalian natural killer receptors (NKRs). NITRs have been identified in multiple bony fish species, including zebrafish, and may be restricted to this large taxonomic group. Thirty-nine NITR genes that can be classified into 14 families are encoded on zebrafish chromosomes 7 and 14. Herein, we demonstrate the expression of multiple NITR genes in the zebrafish ovary and during embryogenesis. All 14 families of zebrafish NITRs are expressed in hematopoietic kidney, spleen and intestine as are immunoglobulin and T cell antigen receptors. Furthermore, all 14 families of NITRs are shown to be expressed in the lymphocyte lineage, but not in the myeloid lineage, consistent with the hypothesis that NITRs function as NKRs. Sequence analyses of NITR amplicons identify known alleles and reveal additional alleles within the nitr1, nitr2, nitr3, and nitr5 families, reflecting the recent evolution of this gene family

Genomic organisation analysis of novel immunoglobulin-like transcripts in Atlantic salmon (Salmo salar) reveals a tightly clustered and multigene family

Copyright 2011 Elsevier B.V., All rights reserved.Peer reviewedPublisher PD

HPTLC simultaneous quantification of triterpene acids for quality control of Plantago major L. and evaluation of their cytotoxic and antioxidant activities

A validated high performance thin-layer chromatography (HPTLC) method was developed for simultaneous determination of ursolic acid (UA) and oleanolic acid (OA) contents in Plantago major which were collected from several plantation areas in Indonesia. The cytotoxic effect against two cancer cell lines, SiHa and Hep G2, and antioxidant activity were evaluated using the MTT and DPPH-radical scavenging assay, respectively. The test samples included various extracts of P. major from different plant parts using methanol and water as extracting solvents and pure compounds derived from this plant. The results showed that both plant parts and extracting solvents affected the chemical contents and their biological activities. The contents of UA and OA varied according to the organs and provenances of plant. The highest content of UA (0.22–0.48% dry weight) and OA (0.17–0.33% dry weight) were found in the methanol extract of seed. This extract also exhibited the highest cytotoxic activity (IC50 value: 174.42–246.38 μg/ml), whereas the strongest free radical scavenging activity was obtained from the leaf methanol extract (IC50 value: 263.57 μg/ml). The developed HPTLC method can be used for routine analysis and standardization of P. major crude drugs, extracts, and/or finished products using UA and OA as appropriate markers for anticancer products