boronophenylalanine bpa uptake assay kit (Dojindo Labs)
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Boronophenylalanine Bpa Uptake Assay Kit, supplied by Dojindo Labs, used in various techniques. Bioz Stars score: 93/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bpa+uptake+assay/pmc12489427-108-9-17?v=Dojindo+Labs
Average 93 stars, based on 17 article reviews
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1) Product Images from "Relationship between amino acid transporter activity and radioactive iodine therapy efficacy in differentiated thyroid cancer"
Article Title: Relationship between amino acid transporter activity and radioactive iodine therapy efficacy in differentiated thyroid cancer
Journal: Oncology Reports
doi: 10.3892/or.2025.8993
Figure Legend Snippet: Analysis of BPA uptake. (A) BPA uptake in plated cells exposed to 8 Gy IR was analyzed using a microplate reader. Data are presented as the mean ± SD of the ratio of the IR group (n=6) relative to the control group (n=10). (B) Representative histogram of BPA uptake in single cells analyzed by flow cytometry. (C) Quantification of BPA uptake in single cells (n=3). *P<0.01 (unpaired Student's t-test). BPA, boronophenylalanine; IR, ionizing radiation.
Techniques Used: Control, Flow Cytometry
![(A) Schematic depiction of the LAT1-dependent uptake assay for import of the amino acid analog π-Boronophenylalanine <t>(L-BPA).</t> Cell were treated with L-BPA for 5min (1) after which cells were extensively washed, followed by the addition of a specific membrane permeable probe for additional 5 min (2), which emits fluorescent signal when bound to L-BPA(3). (B) Graph shows L- <t>BPA</t> <t>uptake</t> by Myd88 KO iBMDMs infected with the indicated Lp strains at MOI=20 or left uninfected (UN). In some control conditions, the LAT1 inhibitor 2-Aminobicyclo [2.2.1] heptane-2-carboxylic acid (BCH) at 1mM was added 10 min prior to and for the duration of the L-BPA uptake assay. BPA uptake lasted 5min and was measured at 4 hpi, after which fluorescence output was measured, the cells were lysed and total protein content was measured. Mean fluorescence data was normalized to the total protein content. Averages ± SEM of data from three biological repeats are shown for each condition. Statistical analysis was completed via one-way ANOVA Kruskal-Wallis test with Dunn’s multiple comparison and the respective p-values among the conditions compared are indicated.](https://bio-rxiv-images-cdn.bioz.com/dois_ending_with_45/10__1101_slash_2025__02__20__639245/10__1101_slash_2025__02__20__639245___F7.large.jpg)