Supplemental Figure 1 A. EpCAM Gating Strategy Top Row: Histogram showing unstained BT474 cells with low fluorescent intensity of the EpCAM specific PE.

Slides:



Advertisements
Similar presentations
Research Techniques Made Simple: Flow Cytometry Richard R
Advertisements

Slide 1, 4/12/2015 of DNA.ppt  Purdue University Cytometry Laboratories DNA1.ppt.
A. a). d). c). f). b).e). g). Figure S1. NAT2 expression in lymphocytes and monocytes from a healthy volunteer. PBMC from a healthy volunteer were simple.
What is Flow Cytometry? Flow Cytometry uic Introduction to Flow Cytometry IGC Workshop Multicolor Flow Cytometry IGC – April 28, 2010 Adapted from Holden.
750LP 780/60 710/ LP 710/50 530/30 Blue Laser (488nm, 100mW)Red laser (644nm,100mW) Alexa 700 APC Cy7 APC-Alexa750 Alexa 488 FITC CFSE SYTOX Green.
FLOW CYTOMETRY Dr. MOHAMMED H SAIEMA LDAHR KAAU FACULTY OF APPLIED MEDICAL SCIENCES MEDICAL TECHNOLOGY DEPT. 2 ND YEAR MT INSTROMINTATION EXT
Introducing a new instrument to the Cancer Center Flow Cytometry Core Facility: The LSR II by Becton Dickinson.
Page 1 © J.Paul Robinson, Purdue University Cytometry Laboratories BMS 602 LECTURE 9.PPT BMS LECTURE 9 Flow Cytometry: Theory Hansen Hall,
Isotype control Supplementary Figure S1. Strategy for gating CD11b+CD14-CD33+CD40+ myeloid cells. Singlets were gated from live cells shown in forward.
Basics of Flow Cytometry Holden Maecker. Outline Definitions, what can be measured by flow cytometry Fluidics: Sheath and sample streams, flow cells,
Cell viability studies Sepideh Khoshnevis. The Goal To distinguish live cells from dead and apoptotic cells in order to calculate the the percentage of.
Flow Cytometry at Boston University Medical Campus Introduction to some methods that we offer Yan Deng (X4-5225), Gerald Denis (X4-1371),
Introduction To Flow Cytometry By Noha Kamel. Flow cytometry is a method of measuring multiple physical and chemical characteristics of particles by optical.
Basic Principles in Flow Cytometry
Laser Flow Cytometry Forward Scatter indicates size Forward Scatter.
Flow Cytometry Basic Training. What Is Flow Cytometry? Flow ~ cells in motion Cyto ~ cell Metry ~ measure Measuring properties of cells while in a fluid.
Flow Cytometry (FCM) Yun-Ju Lee September 13, 2002.
IFNγIL-2TNFaIL-17A CD40 L MOPP DMSO CD4+ Supplemental figure 5A SEB isotype control isotype control isotype control CD69+ A.
FLOW CYTOMETRY Not as scary as it sounds!. A BIT OF HOUSEKEEPING…  About me!  About you  Institute  Prior knowledge  Core facility.
% % % TcFc1: Expression of CD3, 4 and 8 T cells were gated according to size and granularity to exclude non-vital cells in.
Flow Cytometry. Applications FRET- protein interaction Membrane protein expression Intracellular protein expression Cell viability Ca 2+
Date of download: 5/31/2016 Copyright © 2016 American Medical Association. All rights reserved. From: Toll-like Receptors in Regulatory T Cells of Patients.
Fluorescence and Fluorochromes Peter O’Toole Tel:
Fluorescence and Fluorochromes Peter O’Toole Tel:
Determination of cytotoxic T lymphocyte activity against
Fluorescence intensity
بسم الله الرحمن الرحیم.
Flow Cytometry Halima Moncrieffe, University College London, UK IL-17
Flowcytometry.
Copyright © 2014 American Medical Association. All rights reserved.
Evaluation of SERS labeling of CD20 on CLL cells using optical microscopy and fluorescence flow cytometry  Christina M. MacLaughlin, BSc, Edward P.K.
Representative flow cytometry dot plots from a healthy individual
FLOWCYTOMETRY.
Default LSR II Configuration BLUE 488nm PerCP, PerCP-Cy5.5, PE-Cy5
Core Facility Operator
Figure 2 Percentage of CD19+/CD34+ cells with decreased CD81 median fluorescence intensity (MFI;
COMPENSATION + FITC - PE - + PE - FITC - FITC detector FITC PE
A B C D CD4+ CD8+ Control Isotype Ab Anti-TNFa Ab Control Isotype Ab
A B C Supplementary Figure 1 Group 1 Group 2 Group 3 #1 #2 #3 #4 #5 #6
Red pulp macrophages in the human spleen are a distinct cell population with a unique expression of Fc-γ receptors by Sietse Q. Nagelkerke, Christine W.
Volume 6, Issue 5, Pages e5 (May 2018)
Residual Cancer Lymphocytes in Patients With Chronic Lymphocytic Leukemia After Therapy Show Increased Expression of Surface Antigen CD52 Detected Using.
A B Supplemental Figure 1 PBMC Cervical Cytobrush
Reticulocyte Detection
Flow Cytometry Journal of Investigative Dermatology
Figure S2 Gating strategy of AT2 cells based on EpCAM and MHCII
Volume 8, Issue 16, Pages (July 1998)
Optical measurement.
Use of EAS to define TCR-Vb3- and TCR-Cb1-expressing T cells
Volume 119, Issue 5, Pages (November 2000)
the common cytokine receptor g chain,
Flow cytometric analysis of putative progenitor cells.
Increased chemokine content and leukocyte infiltrate in D6-negative tumors. Increased chemokine content and leukocyte infiltrate in D6-negative tumors.
Label-Retaining Cells (Presumptive Stem Cells) of Mice Vibrissae Do Not Express Gap Junction Protein Connexin 43  Maja Matic, Marcia Simon  Journal of.
The Art of Flow Cytometry
Figure S1. Representative gating of 7-hr suppression assay from one subject Teff with media alone (top row), Teff with activation beads but not Tregs (middle),
Supplemental Digital Content 2 – Figure 1
Flow cytometry analysis of TNF-β- and IL-10-producing CD33+ cells.
Supplemental Digital Content 3 – Figure 2
Postoperative changes in blood monocyte subsets.
(A) HLA-E expression on the surface of CD14+ cells in patients with AS, HLA-B*2705, HLA-B*2709-positive and HLA-B27-negative HCs. Results are expressed.
Residual Cancer Lymphocytes in Patients With Chronic Lymphocytic Leukemia After Therapy Show Increased Expression of Surface Antigen CD52 Detected Using.
Figure 1 CD52 expression on innate myeloid and lymphoid cell subsets
Lack of Membrane Expression of Interleukin-2 Receptor α Chain (CD25) in Mycosis Fungoides: Application of Laser Scanning Cytometry for Phenotyping of.
1. Use the brightest fluorophores available. Brightness Expression
PD-L1 expression by DC subsets from lesional CTCL and healthy skin.
Flow cytometry analysis of intracellular cytokine expression in control PBMC (left set of panels) and following either PMA-ionomycin activation (middle.
S.varasteh 10/11/2012.
Hypoxia upregulates CD137 expression in T lymphocytes undergoing activation. Hypoxia upregulates CD137 expression in T lymphocytes undergoing activation.
Alinne Colin, M. D. , Gerardo Barroso, M. D. , M. Sc
Presentation transcript:

Supplemental Figure 1 A. EpCAM Gating Strategy Top Row: Histogram showing unstained BT474 cells with low fluorescent intensity of the EpCAM specific PE Fluorochrome (488nm laser, 585/42-A emission filter) (x axis; y axis = CD45 PE Cy7, 488 nm laser, 780/60-A emission filter). The corresponding unstained cytometry enumeration gate displayed no EpCAM positive populations. Bottom Row: Histogram showing EpCAM Antibody stained BT474 cells with high fluorescent intensity in the PE Fluorochrome channel. Stained cells vastly populating the EpCAM positive enumeration gate.

Supplemental Figure 1 B. Thioflavin Gating Strategy Top Row: Histogram showing unstained BT474 cells with low fluorescent intensity of the Thioflavin specific PE Fluorochrome (407nm laser, 530/30-A emission filter) (x axis; y axis = Side Scatter Profile). The corresponding unstained cytometry enumeration gate displayed no Thioflavin positive populations. Bottom Row: Histogram showing Thioflavin Antibody stained BT474 cells with high fluorescent intensity in the Pacific Orange Fluorochrome channel. Stained cells clearly displaying right shift when compared to Unstained cells.

Supplemental Figure 1 C. CD45 Gating Strategy Top Row: Histogram showing unstained BT474 cells with low fluorescent intensity of the CD45 specific PE Fluorochrome (407nm laser, 530/30-A emission filter) (x axis; y axis = Side Scatter Profile). The corresponding unstained cytometry enumeration gate displayed no CD45 positive populations. Bottom Row: Histogram showing CD45 Antibody stained BT474 cells with low fluorescent intensity in the PECy7 Fluorochrome channel. Stained cells clearly displaying no apparent shift when compared to unstained cells, thus demonstrating no expression of leukocyte-specific CD45 Antibody on BT474 cells.