12-0338-41

antibody from Invitrogen Antibodies

Targeting: CD33 FLJ00391, p67, SIGLEC-3, SIGLEC3

Provider product page for 12-0338-41

Flow cytometry

Other assay

Antibody data

Antibody Data
Antigen structure
References [14]
Comments [0]
Validations
Flow cytometry [1]
Other assay [9]

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Product number: 12-0338-41 - Provider product page
Provider: Invitrogen Antibodies
Product name: CD33 Monoclonal Antibody (WM-53 (WM53)), PE, eBioscience™
Antibody type: Monoclonal
Antigen: Other
Description: Description: The WM-53 monoclonal antibody reacts with human CD33, also known as GP67 and P67, a 67 kDa type I transmembrane glycoprotein that is a member of the Siglec (sialic acid-binding Ig superfamily lectin) family. It is highly specific to the hematopoietic compartment and is expressed on monocytes, activated T cells, granulocytes, myeloid progenitors, and mast cells.
Conjugate: Yellow dye
Antibody clone number: WM-53 (WM53)
Concentration: 5 µL/Test

CD33 protein structure - 12-0338-41 shown in red.

Supportive validation

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Experimental details: NULL
Conjugate: Yellow dye

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
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Experimental details: NULL
Conjugate: Yellow dye

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
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Experimental details: Fig. 1 METTL3 expression and CD33 + MDSC distribution in patients with CC. a , b The immunohistochemical staining for METL3 and CD33 CC specimens (x 400). c The isotype antibody IgG was included (x 400). d Immunofluorescence staining for METTL3 (red) and CD33 + (green) in CC specimens; the white arrows point to the METTL3 + and CD33 + cells. The images were taken by fluorescence microscope. HLA-DR - CD33 + CD11b + cells were gated by a FACS gating strategy and were defined as MDSCs in this study. e , f Representative density plots showed the MDSC population in the peripheral blood of healthy donors (HD) or CC patients, as well as in the immune cells from tumour tissues (TIL) or tumour-adjacent tissues (NIL). A statistical graph is included for the comparison between the indicated groups. (G-H) Representative immunoblotting shows the expression of METTL3 in the peripheral blood, TILs and NILs. A statistical graph is included for the comparison between the indicated groups. The experiments in e , f were performed at least three times, and the data were plotted as the mean +- SEM. Statistics were conducted with an unpaired Student''s t test, * P < 0.05, and *** P < 0.001 vs. the corresponding control
Conjugate: Yellow dye

Supportive validation

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Experimental details: Figure 2 Phenotypic analysis of LDGs and NDGs. LDGs and NDGs were isolated as described in materials and methods (n = 22) and the expression levels of CD11b (A), CD15 (B), CD33 (C), CD66b (D), CD16 (E), CD13 (F), CD63 (G) and arginase 1 (H) were determined by flow cytometry. Isotype controls:
Conjugate: Yellow dye

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
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Experimental details: Fig. 2 The effect of intra- and extra-cellular Gal-9 on MDSC differentiation and expansion in vitro. ELISA assay of IL-6 and IL-1beta concentrations in the conditioned media of TW03-EV and TW03-Gal-9 cells or CD33 + cells ( a ) or Gal-9 knockdown (shGal9-01 and shGal9-02) and control C666-1 cells ( b ) with or without addition of human recombinant Gal-9 (hR-Gal-9). c Differentiation of CD33 + cells isolated from healthy PBMCs investigated after treatment with control medium, co-cultivation with TW03-EV or TW03-Gal-9. Representative flow cytometry plots ( left ) and histogram ( right ) of MDSC differentiation assays showing the percentage of CD33 + CD11b + cells in the HLA-DR - gate arising from CD33 + cells. d Similar experiment based on co-cultivation with C666-1 cells using four experimental conditions: C666-1-shCtrl cells (shCtrl), unmodified C666-1-shGal9-01 (shGal-9), C666-1-shGal9-01 co-transfected with a control lentiviral vector (shGal9 + EV) or a Gal-9 lentiviral vector (ShGal-9+Gal-9). e Representative flow cytometry plots ( left ) and histogram ( right ) of MDSC differentiation assays showing the percentage of CD33 + CD11b + cells in the HLA-DR - gate arising from CD33 + cells with or without addition of human recombinant Gal-9 (hR-Gal-9). f Representative flow cytometry plots ( left ) and histogram ( right ) of the IFN-gamma-positive, proliferating T cells (CSFE assay) to test the immune-suppressive activity of MDSC cells induced by TW03-EV and TW03-Gal-9 or C666-
Conjugate: Yellow dye

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
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Experimental details: Fig. 3 Endogenous Gal-9 downregulates STING leading to tumor-associated MDSC expansion depending on cytokine-induction. a The extracts of TW03 cells stably expressing Flag-tagged-EV or Gal-9 (left) and CD33 + cells transfected with lenti-flag-tagged-EV or lenti-flagged-Gal-9 vector (right) were subjected to immunoblot with the indicated antibodies. b Upper panel: the lysates of TW03 cells and CD33 + cells expressing Flag-tagged EV or Gal-9 were subjected to immunoblot with the indicated antibodies. Lower panel: RT-PCR analysis of STING mRNA; GAPDH mRNA served as a transcript of reference. c The lysates of C666-1 cells transfected with Gal-9-specific shRNAs were subjected to immunoblot with the indicated antibodies. The mRNA expression levels of ISG genes were determined in TW03 cells transfected with the Gal-9-expressing vector or EV ( d ) C666-1 cells transfected with shRNA targeting Gal-9 ( e ) or corresponding control vectors using quantitative real time PCR (qRT-PCR). f ELISA assay of IL-6 and IL-1beta concentrations in the supernatants from control or STING-KO TW03 cells, transfected with Flag-EV and Flag-Gal-9 for 48 h. g Representative flow cytometry plots ( left ) and histogram ( right ) of MDSC differentiation assay for CD33 + cells co-cultured with Control (Ctrl) or STING-KO TW03 cells, transfected with Flag- EV or Flag-Gal-9 for 48 h. All experiments were performed at least three times, and the quantification data were plotted as the mean +- SEM. Statistics were co
Conjugate: Yellow dye

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
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Experimental details: Figure 1 gMDSC expand in subjects replicating HBV in the absence of immunopathology a ) Sequential gating strategy for gMDSC identification (CD11b high CD33 + HLA-DR - CD14 - CD15 + ) using 11-color flow cytometry from freshly isolated PBMC (doublet discrimination not shown). gMDSC population (superimposed in red) was calculated as a percentage of myeloid cells (CD11b high CD33 + ). Cumulative dot plots showing circulating b ) gMDSC and c ) mMDSC frequencies (n=44, healthy controls; n=84, CHB). d ) gMDSC frequencies analyzed by gender. e ) Summary plot of frequencies classified by disease phase using a subset of the cohort with clearly defined disease phases: 14 ""immunotolerants"" (HBeAg + , HBV DNA >10 7 IU/ml, ALT 5x10 5 IU/ml, ALT >60 IU/L), 21 ""inactive disease"" (HBeAg - , HBV DNA 60 IU/L). f ) gMDSC frequencies according to hepatic necroinflammatory score (n=42, CHB). g ) Unsupervised hierarchical clustering using Euclidean distance; dendrogram displaying similarity between clusters. Clinically assigned disease phase, shown adjacent to plot; immunotolerant: dark green, eAg + active disease: dark yellow, inactive disease: pale green, eAg - active disease: pale yellow (not used for analysis). Increasing color intensity (blue-red) corresponds to increasing gMDSC frequency, ALT (IU/L) or necroinflammatory score (n=42, CHB; maximum
Conjugate: Yellow dye

Supportive validation

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Experimental details: Figure 5 iPSCs Derived from Different Donors Show Variable Erythroid Lineage Differentiation Propensity (A) Representative micrographs showing the hematopoietic cells differentiated from iPSCs with reduced hemoglobinized erythroid cells in iPSCs derived from T42 (left panel). Scale bar, 100 mum. (B) Representative FACS plots of differentiated genetically matched F- and B-iPSC lines (n = 4) showing the percentage of erythroblasts (GPA+ CD71+ gated from CD45- CD33-). (C) Scatter graphs presenting percentage of erythroblasts generated from the genetically matched F- and B-iPSC lines. Each dot represents an independent experiment. (D) Percentage of erythroid colonies out of the total colony number generated from iPSC lines. Values are mean +- SEM. Statistics performed by Student's t test, in three or four biological replicates. (E) Gene set enrichment plot and heatmap showing the genes constituting the core enrichment of overlap between multi-potent progenitors sorted from the bone marrow of DBA patients and iPSC lines derived from T42 cells. T42 iPSC lines show decreased expression levels of genes that are downregulated in Diamond-Blackfan anemia patients.
Conjugate: Yellow dye

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
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Experimental details: Figure 1 Unfractionated PBMC contain highly serviceable, readily activated myeloid Ag-presenting cells A . Cryopreserved healthy donor PBMC derived by leukapheresis were thawed on d0, cultured overnight in RPMI 1640 with standard additives,10% heat deactivated human AB serum, 40ng/ml rhGM-CSF and 20ng/ml rhIL-4, then exposed on d1 to single or paired danger signals (pIC 50mug/ml, R848 10muM, LPS 50ng/ml, IFNgamma 2000 IU/ml). Supernatants were harvested for ELISA on d2 to determine production of IL-12 (functionally assembled IL-12p70 dimer), pg/ml, 6 million PBMC/ml. This is representative of 8 biological replicates. B . Scheme depicting Steps 1 and 2 of culture for groups receiving rhGM-CSF+R848+LPS. C . d2 analyses of PBMC cultured three different ways: (a) standard ""IL-12"" culture group (2 days prior to their initial exposure to rhIL-12 and rhIL-2); (b) ""GM"" conditioned culture group which received rhGM-CSF (40 ng/ml) on d0; (c) ""GM+R848+LPS"" group, same as ""GM"" group but also receiving R848+LPS on d1. d2 supernatants were assayed for IL-12p70 and IL-23 (BD = below detection) and resuspended PBMC were analyzed by FACS for B7.1 and HLA-DR expression within the CD33+ myeloid subpopulation. Mean fluorescent indices (MFI) were normalized relative to isotype control values of 1.0, and are representative of 5 biological replicates. D . Same groups as in C ., carried forward in culture after pulsation either with Candida albicans extract at a 1:10 dilution (CAN) or with r
Conjugate: Yellow dye