Human TRA-1-85/CD147 PE-conjugated Antibody Summary
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of TRA‑1‑85/CD147 in Human PBMCs by Flow Cytometry. Human peripheral blood lymphocytes and monocytes were stained with either (A) Mouse Anti-Human TRA-1-85/CD147 PE-conjugated Monoclonal Antibody (Catalog # FAB3195P) or (B) Mouse IgG1Phycoerythrin Isotype Control (Catalog # IC002P). View our protocol for Staining Membrane-associated Proteins.
Detection of Mouse TRA-1-85/CD147 by Flow Cytometry Flow cytometry analysis of total cell fractions of dissociated cells from PDX models.A) Basal-like xenograft cells. B) Luminal-like xenograft cells. A and B displays pseudo-color dot plots (left panels) and histograms (right panels). Freshly harvested xenografts were minced and the whole cell suspensions were washed and stained with monoclonal antibody towards EpCAM, TRA-1-85 (filled blue in histograms), H2-kd (red line in lower histogram) and Hoecst-33342 (intensity measure for DNA content of cells, grey contours in both histograms. Left peak indicate mouse cells, right peak indicate human cells). The population positive for both EpCAM and TRA-1-85, i.e the human tumor cells, are indicated with a circle in the dot plots. C) Flow cytometry analysis of double stained samples (marker of interest and EpCAM/Tra-1-85) of the Luminal-like PDX model. Flow cytometry histograms show the distribution of the markers indicated in the figure. Filled blue histogram represents EpCAM positive tumor cell population, and the EpCAM negative population (mouse stroma cells) is indicated by the red line. Grey contour represent unstained control. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/25419568), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of Mouse TRA-1-85/CD147 by Flow Cytometry Flow cytometry analysis of total cell fractions of dissociated cells from PDX models.A) Basal-like xenograft cells. B) Luminal-like xenograft cells. A and B displays pseudo-color dot plots (left panels) and histograms (right panels). Freshly harvested xenografts were minced and the whole cell suspensions were washed and stained with monoclonal antibody towards EpCAM, TRA-1-85 (filled blue in histograms), H2-kd (red line in lower histogram) and Hoecst-33342 (intensity measure for DNA content of cells, grey contours in both histograms. Left peak indicate mouse cells, right peak indicate human cells). The population positive for both EpCAM and TRA-1-85, i.e the human tumor cells, are indicated with a circle in the dot plots. C) Flow cytometry analysis of double stained samples (marker of interest and EpCAM/Tra-1-85) of the Luminal-like PDX model. Flow cytometry histograms show the distribution of the markers indicated in the figure. Filled blue histogram represents EpCAM positive tumor cell population, and the EpCAM negative population (mouse stroma cells) is indicated by the red line. Grey contour represent unstained control. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/25419568), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of Mouse TRA-1-85/CD147 by Flow Cytometry Flow cytometry analysis of total cell fractions of dissociated cells from PDX models.A) Basal-like xenograft cells. B) Luminal-like xenograft cells. A and B displays pseudo-color dot plots (left panels) and histograms (right panels). Freshly harvested xenografts were minced and the whole cell suspensions were washed and stained with monoclonal antibody towards EpCAM, TRA-1-85 (filled blue in histograms), H2-kd (red line in lower histogram) and Hoecst-33342 (intensity measure for DNA content of cells, grey contours in both histograms. Left peak indicate mouse cells, right peak indicate human cells). The population positive for both EpCAM and TRA-1-85, i.e the human tumor cells, are indicated with a circle in the dot plots. C) Flow cytometry analysis of double stained samples (marker of interest and EpCAM/Tra-1-85) of the Luminal-like PDX model. Flow cytometry histograms show the distribution of the markers indicated in the figure. Filled blue histogram represents EpCAM positive tumor cell population, and the EpCAM negative population (mouse stroma cells) is indicated by the red line. Grey contour represent unstained control. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/25419568), licensed under a CC-BY license. Not internally tested by R&D Systems.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, 2 to 8 °C as supplied.
Background: TRA-1-85/CD147
The TRA-1-85 antigen, also known as OKa blood group antigen, is a specific epitope within the protein known as Basigin, EMMPRIN and CD147. It is a cell surface determinant expressed on almost all human cell types. This antibody has been used in somatic cell hybrid studies to identify tissues of partial human origin (1, 2).
Product Datasheets
Citations for Human TRA-1-85/CD147 PE-conjugated Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 7
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TET1 facilitates specification of early human lineages including germ cells
Authors: Fei-Man Hsu, Qiu Ya Wu, Emily B. Fabyanic, Alex Wei, Hao Wu, Amander T. Clark
iScience
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Generation of three human induced pluripotent stem cell sublines (UCLAi004-A, UCLAi004-B, and UCLAi004-C) for reproductive science research
Authors: EC Pandolfi, TJ Hunt, S Goldsmith, K Hurlbut, SJ Silber, AT Clark
Stem Cell Research, 2021-06-24;54(0):102446.
Species: Human
Sample Types: Whole Cells
Applications: ICC -
Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research
Authors: EC Pandolfi, TJ Hunt, S Goldsmith, K Hurlbut, SJ Silber, AT Clark
Stem Cell Research, 2021-06-08;54(0):102409.
Species: Human
Sample Types: Whole Cells
Applications: IHC -
Generation of three human induced pluripotent stem cell sublines (MZT04D, MZT04J, MZT04C) for reproductive science research
Authors: EC Pandolfi, EJ Rojas, E Sosa, JJ Gell, TJ Hunt, S Goldsmith, Y Fan, SJ Silber, AT Clark
Stem Cell Res, 2019-09-16;40(0):101576.
Species: Human
Sample Types: Whole Cells
Applications: Flow Cytometry -
Differential in vivo tumorigenicity of distinct subpopulations from a luminal-like breast cancer xenograft.
Authors: Skrbo N, Hjortland G, Kristian A, Holm R, Nord S, Prasmickaite L, Engebraaten O, Maelandsmo G, Sorlie T, Andersen K
PLoS ONE, 2014-11-24;9(11):e113278.
Species: Human
Sample Types: Whole Cells
Applications: Flow Cytometry -
Maturation, not initiation, is the major roadblock during reprogramming toward pluripotency from human fibroblasts
Authors: Koji Tanabe, Michiko Nakamura, Megumi Narita, Kazutoshi Takahashi, Shinya Yamanaka
Proceedings of the National Academy of Sciences
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Three-dimensional culture systems for the expansion of pluripotent embryonic stem cells.
Authors: Storm MP, Orchard CB, Bone HK, Chaudhuri JB, Welham MJ
Biotechnol. Bioeng., 2010-11-01;107(4):683-95.
Species: Human
Sample Types: Whole Cells
Applications: Flow Cytometry, ICC
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