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antibody from Invitrogen Antibodies
Targeting: CLEC7A
CD369, CLECSF12, dectin-1, hDectin-1, SCARE2
Flow cytometryAntibody data
- Antibody Data
- Antigen structure
- References [5]
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- Validations
- Flow cytometry [1]
- Other assay [3]
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- Product number
- 46-9856-42 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- CD369 (Clec7a, Dectin-1) Monoclonal Antibody (15E2), PerCP-eFluor 710, eBioscience™
- Antibody type
- Monoclonal
- Antigen
- Other
- Reactivity
- Human
- Host
- Mouse
- Isotype
- IgG
- Antibody clone number
- 15E2
- Vial size
- 100 Tests
- Concentration
- 5 µL/Test
- Storage
- 4° C, store in dark, DO NOT FREEZE!
Submitted references High-Yield Human Induced Pluripotent Stem Cell-Derived Monocytes and Macrophages Are Functionally Comparable With Primary Cells.
The Correlation of CD206, CD209, and Disease Severity in Behçet's Disease with Arthritis.
Isoform localization of Dectin-1 regulates the signaling quality of anti-fungal immunity.
MiR-146a negatively regulates dectin-1-induced inflammatory responses.
Porphyromonas gingivalis evasion of autophagy and intracellular killing by human myeloid dendritic cells involves DC-SIGN-TLR2 crosstalk.
Cui D, Franz A, Fillon SA, Jannetti L, Isambert T, Fundel-Clemens K, Huber HJ, Viollet C, Ghanem A, Niwa A, Weigle B, Pflanz S
Frontiers in cell and developmental biology 2021;9:656867
Frontiers in cell and developmental biology 2021;9:656867
The Correlation of CD206, CD209, and Disease Severity in Behçet's Disease with Arthritis.
Choi B, Suh CH, Kim HA, Sayeed HM, Sohn S
Mediators of inflammation 2017;2017:7539529
Mediators of inflammation 2017;2017:7539529
Isoform localization of Dectin-1 regulates the signaling quality of anti-fungal immunity.
Fischer M, Müller JP, Spies-Weisshart B, Gräfe C, Kurzai O, Hünniger K, Hochhaus A, Scholl S, Schnetzke U
European journal of immunology 2017 May;47(5):848-859
European journal of immunology 2017 May;47(5):848-859
MiR-146a negatively regulates dectin-1-induced inflammatory responses.
Du L, Chen X, Duan Z, Liu C, Zeng R, Chen Q, Li M
Oncotarget 2017 Jun 6;8(23):37355-37366
Oncotarget 2017 Jun 6;8(23):37355-37366
Porphyromonas gingivalis evasion of autophagy and intracellular killing by human myeloid dendritic cells involves DC-SIGN-TLR2 crosstalk.
El-Awady AR, Miles B, Scisci E, Kurago ZB, Palani CD, Arce RM, Waller JL, Genco CA, Slocum C, Manning M, Schoenlein PV, Cutler CW
PLoS pathogens 2015 Feb;10(2):e1004647
PLoS pathogens 2015 Feb;10(2):e1004647
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Staining of normal human peripheral blood cells with Anti-Human CD14 FITC (Product # 11-0149-42) and Anti-Human/Non-Human Primate CD369 (Clec7a, Dectin-1) PerCP-eFluor® 710. Cells in the lymphocyte and monocyte gate were used for analysis.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- NULL
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 1 Ca IG induces the transcription and expression of IL-6, TNFalpha involving the dectin-1-Syk pathways ( A ) RNA was harvested at 0, 1, 3, 6, 24 hours after treated with 100 mug/ml Ca IG and subjected to gene expression analysis by qRT-PCR normalized to beta-actin expression. For both genes analyzed, the significant difference of the Ca IG treated cells was compared with the corresponding untreated cells. ( B ) The culture medium of THP-1 cells treated with 100 mug/ml Ca IG for 24 hours was analyzed by ELISA to determine the protein level of IL-6 and TNFalpha. ( C ) The expression of dectin-1 in THP-1 cells. The THP-1 cells (2 x 10 5 cells) were incubated with anti-human primate Dectin-1 monoclonal antibody for flow cytometric analysis. ( D ) Representative images of Western Blot analyses of p-Syk, Syk, p-IkappaBalpha, IkappaBalpha, p-p38 and p38 protein levels. Protein extracts were made from untreated cells and from Ca IG treated cells for 30, 60 and 90 minutes. Extracted protein samples (50 mug per lane) were subjected to electrophoresis and immunoblotting with antibodies specific for the 6 proteins and beta-actin as control for equal loading. ( E ) NF-kappaB p65 translocation was analyzed by staining with NF-kappaB-p65 (red); and nucleuses were colored with DAPI (blue). Scale bar = 20 mum. ( F ) THP-1 cells were transfected with dectin-1 specific siRNA (siRNA-dectin-1) or scrambled control siRNA (NC) for 48 hours, and were subsequently treated with Ca IG for 6 hour
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- FIGURE 5 Crispr/Cas knockout (KO) and of immune regulatory receptors in human induced pluripotent stem cells (hiPSCs) and functional analysis of macrophages derived from relative KO clones. (A) Workstream scheme for generating and analyzing of single cell KO clones in hiPSC. (B) Eight out-of-frame homozygous Dectin-1 KO clones were identified by Sanger sequencing and interference of CRISPR edits (ICE) analysis. (C) Macrophage marker expression level between wild type (WT) and Dectin-KO clone No. 32-derived macrophages. (D) Dectin-1 expression level and relative isotype in macrophages derived from WT and Dectin-1 KO clone No. 32.
