CD45 antibody | IBL-3/16
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of mouse leukocytes by flow cytometry.
Image caption:
Infiltration of GFP+ BM-cells in infarct and peri-infarct regions. (A-B) Dot plots of viable macrophages/granulocytes (CD11b+CD45high, top right quadrants) and microglia (CD11b+CD45dim, bottom right quadrants) in cortex from BM-chimeric unmanipulated mice and mice exposed to pMCAO. (C) Bar graph showing mean numbers of CD11b+CD45dim microglia and CD11b+CD45high macrophages/granulocytes in BM-chimeric mice 24 hours after pMCAO, subdivided based on expression of GFP (n = 5). Approximately 92% of of the CD45high population were GFP+ . (D) Estimation and comparison of mean numbers of CD11b+CD45dim microglia in non-chimeric (n = 10) versus BM-chimeric mice (n = 5) 24 hours after of pMCAO shows significantly fewer CD11b+CD45dim microglial cells in irradiated mice. (E) Overview, showing distribution of infiltrating GFP+ BM-derived cells into infarct (IF) and peri-infarct (P-IF) regions 24 hours after pMCAO. (E-G) By 24 hours, GFP+ single cells (F) and vessel-associated aggregates of GFP+ cells (arrows in G) were observed in infarct and peri-infarct regions. Some of the vessel-associated cells were round, leukocyte-like cells (arrows) while others were elongated cells lining the vasculature (arrow heads in G and in insert). (H) Bar graph showing mean numbers of single GFP+ cells and vessel-associated aggregates of GFP+ cells in ipsi- and contralateral cortex 24 hours after surgery (n = 10). (I-P) Immunohistochemical staining of CD45.1 (I, K), CD45.2 (J, L), IgG2a (M, O) and CD45 (N, P) in ischemic tissue in BM-chimeric (I, J, M, N) and non-chimeric mice (K, L, O, P) 24 hours after pMCAO. N.D, none detected. Scale bars: 200 μm (A), 10 μm (B, C). 50 μm (I-P) *P <0.05, **P <0.01, and ***P <0.001.
From: Clausen BH, Lambertsen KL, Babcock AA, Holm TH, Dagnaes-Hansen F, Finsen B.
Interleukin-1beta and tumor necrosis factor-alpha are expressed by different subsets of microglia and macrophages after ischemic stroke in mice.
J Neuroinflammation. 2008 Oct 23;5:46.
This image is from an open access article distributed under the terms of the Creative Commons Attrib rel="noopener"ution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of murine leukocytes by flow cytometry.
Image caption:
Inflammatory response following permanent MCA occlusion. (A-C) Dot plots of viable CD11b+CD45high macrophages/granulocytes (top right quadrants) and CD11b+CD45dim microglia (bottom right quadrants) in cortex from unmanipulated control mice (A, B), and mice exposed to pMCAO with 24 hour survival (C). (D) At 24 hours, flow cytometric analysis of the CD11b+CD45high profiles showed that approximately half of the population consisted of CD45highGr1+ granulocytes. (E) Quantification of CD11b+CD45dim and CD11b+CD45high cells in unmanipulated control mice (n = 10), in mice 6 (n = 7), 12 (n = 7), or 24 hours after pMCAO (n = 10), and in sham-operated mice 24 hours after pMCAO (n = 7). (F) Bar graphs showing equal recruitment of CD11b+CD45highGr1- macrophages and CD11b-CD45highGr1+ granulocytes in unmanipulated mice, in mice 6, 12, or 24 hours after pMCAO, and in sham-operated mice 24 hours after pMCAO. (G, H) Bar graphs showing the mean fluorescent intensity (MFI) of CD45 expression by CD45dim microglia (G) and CD45high macrophages/granulocytes (H). *P <0.05, **P <0.01, and ***P <0.001.
J Neuroinflammation. 2008 Oct 23;5:46. doi: 10.1186/1742-2094-5-46.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of murine leukocytes by flow cytometry.
Image caption:
Cytokine expression in segregated populations of cells following stroke. (A, B) Dot plots showing CD11b+CD45high macrophages/granulocytes (upper right quadrants) and CD11b+CD45dim microglia (bottom right quadrants) expressing IL-1β (A) or TNF-α (B). (C-J) Bar graphs showing numbers and proportions of IL-1β (C, D), TNF-α (F, G) and IL-1β/TNF-α co-expressing (I, J) CD11b+CD45dim microglia and CD11b+CD45high macrophages/granulocytes in unmanipulated control mice (n = 10), in mice 6 (n = 7), 12 (n = 7), or 24 hours after pMCAO (n = 10), and in sham-operated mice 24 hours after pMCAO (n = 7). (E, H) Comparison of the MFI values for IL-1β (E) and TNF-α (H) in viable CD11b+CD45dim microglia and CD11b+CD45high macrophages/granulocytes in unmanipulated mice, in mice 6, 12, or 24 hours after pMCAO, and in sham-operated mice 24 hours after pMCAO. Macrophages/granulocytes express significantly more IL-1β than do microglial in unmanipulated mice, in mice 6, 12, or 24 hours after pMCAO, and in sham-operated mice 24 hours after pMCAO (E), whereas microglial cells express significantly higher levels of TNF-α than do macrophages/granulocytes at 12 h and 24 hours, and in sham-operated mice 24 hours after pMCAO (H). (K) CD11b+CD45highGr1- macrophages and not CD11b+CD45highGr1+ granulocytes are the main producers of IL-1β and TNF-α 24 hours after pMCAO. *P <0.05, **P <0.01, and ***P <0.001.
From: Clausen BH, Lambertsen KL, Babcock AA, Holm TH, Dagnaes-Hansen F, Finsen B.
Interleukin-1beta and tumor necrosis factor-alpha are expressed by different subsets of microglia and macrophages after ischemic stroke in mice.
J Neuroinflammation. 2008 Oct 23;5:46. doi: 10.1186/1742-2094-5-46.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of leukocytes by flow cytometry.
Image caption:
Sensitivity of cytokine detection using flow cytometry. Histograms and dot plots of IL-1β (A) and TNF-α (B) expression in LPS-activated peritoneal macrophages versus macrophages/granulocytes isolated from cortex 24 hours after pMCAO. Light colored histograms represent cells stained with isotype control antibodies and filled histograms represent cells stained with antibodies for either IL-1β (A) or TNF-α (B).
From: Clausen BH, Lambertsen KL, Babcock AA, Holm TH, Dagnaes-Hansen F, Finsen B.
Interleukin-1beta and tumor necrosis factor-alpha are expressed by different subsets of microglia and macrophages after ischemic stroke in mice.
J Neuroinflammation. 2008 Oct 23;5:46.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of microglia using immunohistochemistry on formalin fixed, paraffin embedded tissue sections..
Image caption
Percentage of microgliosis (mean ± s.e.m) by area in (a) Tg APPsw/CD40 def. mice versus Tg APPsw mice and in (b) Tg PSAPP/CD40 def. mice versus Tg PSAPP mice at 22 to 24 months of age calculated by quantitative image analysis. Post hoc comparison between groups are indicated by the marked bars (* p <0.05; ** p <0.01). Representative photographs of brain area in (c) Tg APPsw, (e) Tg APPsw/CD40 def., (d) Tg PSAPP and (f) Tg PSAPP/CD40 def. mice stained with CD45 antibody (each bar represents 0.1 mm).
From: Laporte V, Ait-Ghezala G, Volmar CH, Mullan M.
CD40 deficiency mitigates Alzheimer's disease pathology in transgenic mouse models.
J Neuroinflammation. 2006 Feb 24;3:3.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the demonstration of microglia busing immunohistochemistry on formalin fixed, paraffin embedded tissue sections.
Image caption
Chronic effects of celastrol on microgliosis in Tg PS1/APPsw mice. A) Representative photomicrographs (taken with a 20× and 60× objective providing a respective magnification of 200× and 600× respectively) depicting the presence of CD45 reactive microglia around Aβ deposits in Tg PS1/APPsw treated with a placebo and celastrol. B) Histogram representing the burden of activated microglia (CD45 positive) in the cortex of Tg PS1/APPsw mice treated with placebo and celastrol pellets. Statistically significant difference in microgliosis burden (P <0.03) was observed between placebo and celastrol treated mice. (* P <0.05).
.From: Paris D, Ganey NJ, Laporte V, Patel NS, Beaulieu-Abdelahad D, Bachmeier C, March A, Ait-Ghezala G, Mullan MJ.
Reduction of beta-amyloid pathology by celastrol in a transgenic mouse model of Alzheimer's disease.
J Neuroinflammation. 2010 Mar 8;7:17.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of microglial cells by immunofluorescence.
Image caption:
Microglial distribution in minocycline-treated and untreated explants. The left panel shows microglial cells (stained with anti-CD45 antibody, green), whereas the right panel depicts both microglial cells and the location of retinal layers (revealed by nuclear staining with Hoechst, blue). A. Microglial cells in the control explants (CT) are frequently seen within the Outer Nuclear Layer (ONL). B. In minocycline-treated explants (MIN), microglial cells are more compact and do not penetrate the ONL. Representative images of at least three different explants per condition. INL, Inner Nuclear Layer; GCL, Ganglion Cell Layer. Scale bar, 50 μm.
From: Ferrer-Martín RM, Martín-Oliva D, Sierra-Martín A, Carrasco M-C, Martín-Estebané M, Calvente R, et al. (2015)
Microglial Activation Promotes Cell Survival in Organotypic Cultures of Postnatal Mouse Retinal Explants.
PLoS ONE 10(8): e0135238.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of microglial cells by immunofluorescence.
Image caption:
PARP-1 activity in untreated (A,B) and minocycline-treated (C,D) retinal explants. The left column shows the labeling with an antibody recognizing Poly-ADP-Ribose polymers (PAR, green) due to activity of the enzyme PARP-1. The central column exhibits microglial cells revealed by anti-CD45 antibody (red). Finally, pictures in the right column merge the two signals and that of Hoechst labeling of the nuclei. Note that minocycline-treatment (MIN) markedly reduces the PAR immunoreactivity of microglial cells in the control (CT) retinal explant. ONL, Outer Nuclear Layer; INL, Inner Nuclear Layer; GCL, Ganglion Nuclear Layer. Representative images of three retinal explants per treatment. Scale bar, 35 μm for A, 10 μm for B, 34 μm for C, and 9 μm for D.
From: Ferrer-Martín RM, Martín-Oliva D, Sierra-Martín A, Carrasco M-C, Martín-Estebané M, Calvente R, et al. (2015)
Microglial Activation Promotes Cell Survival in Organotypic Cultures of Postnatal Mouse Retinal Explants.
PLoS ONE 10(8): e0135238.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of microglial cells by immunofluorescence.
Image caption:
Effects of LPS treatment on retinal explants.
A: The release of TNF-α was significantly increased in explants treated with LPS (LPS, gray bar) with respect to untreated explants (CT, black bar). Bars represent mean values of 12 explants per condition ± SEM. *** indicates significant differences (P<0.001, Student's t-test). B: Incubation with LPS (LPS, gray bar) also greatly augmented the proportion of proliferating microglial cells (labeled with anti-CD11b and anti-Ki67) with respect to control explants (CT, black bar). Bars represent mean percentages of 5 explants per condition ± SEM; *** indicates significant differences (P<0.001, Student's t-test). C: The PAR immunostaining (green) in LPS explants was similar to that observed in the untreated explants. Pictures in C are representative of 3 explants per condition. ONL, Outer Nuclear Layer; INL, Inner Nuclear Layer; IPL, Inner Plexiform Layer; GCL, Ganglion Cell Layer. Scale bar, 30 μm.
From: Ferrer-Martín RM, Martín-Oliva D, Sierra-Martín A, Carrasco M-C, Martín-Estebané M, Calvente R, et al. (2015)
Microglial Activation Promotes Cell Survival in Organotypic Cultures of Postnatal Mouse Retinal Explants.
PLoS ONE 10(8): e0135238.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of microglial cells by immunofluorescence.
Image caption:
LPS treatment does not modify the distribution of microglial cell and cell viability.
A, B: Distribution of microglial cells in control (A, CT) and LPS-treated (B, LPS) retinal explants. Left panels display microglial cells labeled with anti-CD45 antibody, while right panels also show cell nuclei stained with Hoechst. The distribution of microglia in LPS-treated explants is similar to that of untreated explants. Representative images of 3 different explants per condition. Scale bar, 50 μm. C: Bar graph showing that LPS treatment has no significant effect on cell viability in retinal explants. Bars represent mean values ± SEM of 5 explants).
From: Ferrer-Martín RM, Martín-Oliva D, Sierra-Martín A, Carrasco M-C, Martín-Estebané M, Calvente R, et al. (2015)
Microglial Activation Promotes Cell Survival in Organotypic Cultures of Postnatal Mouse Retinal Explants.
PLoS ONE 10(8): e0135238.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of microglial cells by immunofluorescence.
Image caption:
The effects of minocycline overcome these of LPS treatment. A: The cell viability in the explants treated with minocycline and LPS (MIN+LPS) is similar to that of explants treated with minocycline alone (MIN). Bars represent mean values ± SEM of 5 explants per condition. B, C: The distribution of microglial cells, as revealed by CD45 immunolabeling (green), is similar between explants treated with minocycline alone (MIN, B) and those treated with minocycline plus LPS (MIN+LPS, C). In addition to microglial cells, images in the right column also show the retinal layers revealed by the Hoechst staining of nuclei. Each image is representative of 3 explants. ONL, Outer Nuclear Layer; INL, Inner Nuclear Layer; GCL, Ganglion Cell Layer. Scale bar, 50 μm.
From: Ferrer-Martín RM, Martín-Oliva D, Sierra-Martín A, Carrasco M-C, Martín-Estebané M, Calvente R, et al. (2015)
Microglial Activation Promotes Cell Survival in Organotypic Cultures of Postnatal Mouse Retinal Explants.
PLoS ONE 10(8): e0135238.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of leukocytes in mouse brain by immunofluorescence.
Image caption:
Cryosectioned brain samples from day 6 p.i. were stained for WNV envelope protein (green), CD45 (as a pan-leukocyte marker; red), and DAPI (blue) and utilized for laser scanning confocal microscopy (20X images are shown and are representative of n = 5 mice per group).
From: Wang P, Bai F, Zenewicz LA, Dai J, Gate D, et al. (2012)
IL-22 Signaling Contributes to West Nile Encephalitis Pathogenesis.
PLoS ONE 7(8): e44153.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of microglial cells by immunofluorescence.
Image caption:
Colocalization of activated microglial cells with Aβ plaques and IL-1β immunoreactivity in the TgAPPsw mice with reduced GRK5. Panels A-C, IF staining of Aβ+ plaques (A, red) and surrounding CD45+ microglial cells (B, green), as well as their merged view (C) in the double mice. Scale bar: 50 μm for panels A-C. Panels D-F, IF staining of Aβ+ plaques (D, red) and surrounding CD11b+ microglial cells (E, green), as well as their merged view (F) in the double mice. Scale bar: 50 μm for panels D-F. Panel G, an example of merged view for CD45 (green) and CD11b/c (clone OX42, red) co-staining of the microglial cells. The image showed that, at least in this particular experimental paradigm, the CD45 antibody stained more specifically for the microglial cell profiles; while the OX42 antibody, in addition to its positive staining of the microglial cells, also non-specifically decorated the plaques. Scale bar: 45 μm. Panel H, an example of merged view for Aβ+ plaques (red) and surrounding IL-1β immunoreactivity (green) in the double mice. Scale bar: 30 μm. Panel I, colocalization of CD45+ microglial cells (green) with IL-1β immunoreactivity (red) in the double mice. Scale bar: 30 μm. Blue indicates reference DAPI staining of nuclei.
From: Li et al.
GRK5 deficiency exaggerates inflammatory changes in TgAPPsw mice.
Li et al.. Journal of Neuroinflammation 2008 5:24.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used for the detection of microglia by immunofluorescence.
Image caption:
Increased CD45+ microglial cells in hippocampus and cortex of the TgAPPsw mice with reduced GRK5. Representative IF results with anti-CD45 staining (green) in hippocampus (A-D) and cortex (F-I) of WT (A &F), heterozygote GRK5KO (B &G), TgAPPsw (C &H), and the double mice (D &I), respectively. Scale bar in panel I is for panels A-D and F-I: 100 μm. Panels E &J, examples of high magnification views of CD45+-microglial cells in hippocampus (E) and cortex (J) of the double mice that show details of activated microglial morphology. Scale bar in panel J is for panels E &J: 20 μm. Blue indicates reference DAPI staining of nuclei.
From: Li L, Liu J, Suo WZ.
GRK5 deficiency exaggerates inflammatory changes in TgAPPsw mice.
J Neuroinflammation. 2008 Jun 3;5:24.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Rat anti Mouse CD45 antibody, clone IBL-3/16 (MCA1388) used to evaluate CD45 expression on mouse microglial cells in vitro by immunofluorescence.
Image caption:
Systemic and central (intracortical) blockade of NKCC1 regulate LPS-induced inflammatory cytokine production in the brain in an opposite manner.The main source of IL-1α and IL-1β in the brain are microglia cells.
Confocal images of Cx3CR1+/GFP brain slices show IL-1α-CD45-P2Y12R (above, red arrowheads) and IL-1β-CD45-P2Y12R (below, red arrowheads) labeled cells after cortical LPS injection-induced inflammation.
From: Tóth K, Lénárt N, Berki P, Fekete R, Szabadits E, Pósfai B, et al. (2022)
The NKCC1 ion transporter modulates microglial phenotype and inflammatory response to brain injury in a cell-autonomous manner.
PLoS Biol 20(1): e3001526.
doi: 10.1371/journal.pbio.3001526
This image is from an open access article distributed under terms of a Creative Commons Attribution License.
Filter by Application:
F P IF ResetRat anti Mouse CD45
- Product Type
- Monoclonal Antibody
- Clone
- IBL-3/16
- Isotype
- IgG1
- Specificity
- CD45
Quick Links:
Antibody Quality and 
Unrivaled 
| Rat anti Mouse CD45 antibody, clone IBL-3/16 recognizes murine Receptor-type tyrosine-protein phosphatase C, also known as CD45, Leukocyte common antigen, T200 or Lymphocyte antigen 5 (Ly5). CD45 is a 1291 amino acid ~175kDa single pass type I transmembrane glycoprotein belonging to the protein -tyrosing phosphatase family. CD45 has two fibronectin type-III domains and two tyrosine protein phosphatase domains (UniProt:: P06800). Multiple isoforms are generated by alternative splicing with isoforms having differing deletions in the N-terminal region (Saga et al. 1987). Rat anti Mouse CD45 antibody, clone IBL-3/16 is expected to recognize all isoforms of murine CD45. Rat anti Mouse CD45 antibody, clone IBL-3/16 has been used successfully for the identification of CD45 in murine samples using Immunohistochemical (both cryo and FFPE), immunofluorescence and western blotting techniques (Kondo et al. 2011, Cuadros et al. 2006). |
- Target Species
- Mouse
- Species Cross-Reactivity
-
Target Species Cross Reactivity Rat Human Chicken - N.B. Antibody reactivity and working conditions may vary between species.
- Product Form
- Purified IgG - liquid
- Preparation
- Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
- Buffer Solution
- Phosphate buffered saline.
- Preservative Stabilisers
- <0.1% Sodium Azide (NaN3)
1% Bovine Serum Albumin - Immunogen
- Purified B cells from mouse lymph nodes.
- Approx. Protein Concentrations
- IgG concentration 0.5 mg/ml
- Fusion Partners
- Spleen cells from an immunized Wistar rat were fused with cells of the SP2/0-Ag14 mouse myeloma cell line
- Regulatory
- For research purposes only
- Guarantee
- 12 months from date of despatch
This product is shipped at ambient temperature. It is recommended to aliquot and store at -20°C on receipt. When thawed, aliquot the sample as needed. Keep aliquots at 2-8°C for short term use (up to 4 weeks) and store the remaining aliquots at -20°C.
Avoid repeated freezing and thawing as this may denature the antibody. Storage in frost-free freezers is not recommended.
Avoid repeated freezing and thawing as this may denature the antibody. Storage in frost-free freezers is not recommended.
This product has been reported to work in the following applications. This information is derived from testing within our laboratories, peer-reviewed publications or personal communications from the originators. Please refer to references indicated for further information. For general protocol recommendations, please visit the antibody protocols page.
| Application Name | Verified | Min Dilution | Max Dilution |
|---|---|---|---|
| Flow Cytometry |  |
1/50 | 1/100 |
| Immunofluorescence | |
||
| Immunohistology - Frozen 1 | |
1/50 | 1/100 |
| Immunohistology - Paraffin | |||
| Immunohistology - Resin | |||
| Immunoprecipitation | |
||
| Western Blotting |
- 1The epitope recognised by this antibody is reported to be sensitive to formaldehyde fixation and tissue processing. Bio-Rad recommends the use of acetone fixation for frozen sections.
Where this antibody has not been tested for use in a particular technique this does not necessarily exclude its use in such procedures. Suggested working dilutions are given as a guide only. It is recommended that the user titrates the antibody for use in their own system using appropriate negative/positive controls.
- Flow Cytometry
- Use 10ul of the suggested working dilution to label 106 cells in 100ul.
References for CD45 antibody
-
Balogh, P. et al. (1995) Modulatory effect of CD45 on the MHC Class II-induced homotypic aggregation of B cells in mice.
In 9th International Congress of Immunology, Abstract book p. 72. No. 422. -
Santos, A.M. et al. (2008) Embryonic and postnatal development of microglial cells in the mouse retina.
J Comp Neurol. 506: 224-39. -
Yan, Q. et al. (2003) Anti-inflammatory drug therapy alters beta-amyloid processing and deposition in an animal model of Alzheimer's disease.
J Neurosci. 23: 7504-9. -
Zehntner, S.P. et al. (2007) X-linked inhibitor of apoptosis regulates T cell effector function.
J Immunol. 2007 Dec 1;179(11):7553-60. -
Neutzner, M. et al. (2007) MFG-E8/lactadherin promotes tumor growth in an angiogenesis-dependent transgenic mouse model of multistage carcinogenesis.
Cancer Res. 67: 6777-85. -
Ozmen, L. 145-2C11 (2005) BACE/APPV717F double-transgenic mice develop cerebral amyloidosis and inflammation.
Neurodegener Dis. 2: 284-98. -
Ideguchi, M. et al. (2008) Immune or inflammatory response by the host brain suppresses neuronal differentiation of transplanted ES cell-derived neural precursor cells.
J Neurosci Res. 86: 1936-43. -
Santos, A.M. et al. (2010) Microglial response to light-induced photoreceptor degeneration in the mouse retina.
J Comp Neurol. 518: 477-92.
View The Latest Product References
-
McMenamin, P.G. <et al. (2006) Characterisation of rat corneal cells that take up soluble antigen: an in vivo and in vitro study.
Exp Eye Res. 83: 1268-80. -
Clausen, B.H. et al. (2008) Interleukin-1beta and tumor necrosis factor-alpha are expressed by different subsets of microglia and macrophages after ischemic stroke in mice.
J Neuroinflammation. 5: 46. -
Laporte, V. et al. (2006) CD40 deficiency mitigates Alzheimer's disease pathology in transgenic mouse models.
J Neuroinflammation. 3: 3. -
Paris, D. et al. (2010) Reduction of beta-amyloid pathology by celastrol in a transgenic mouse model of Alzheimer's disease.
J Neuroinflammation. 7: 17. -
Kondo, Y. et al. (2011) Macrophages counteract demyelination in a mouse model of globoid cell leukodystrophy.
J Neurosci. 31: 3610-24. -
Boger, H.A. et al. (2007) Long-term consequences of methamphetamine exposure in young adults are exacerbated in glial cell line-derived neurotrophic factor heterozygous mice.
J Neurosci. 27: 8816-25. -
Boger, H.A. et al. (2009) Minocycline restores striatal tyrosine hydroxylase in GDNF heterozygous mice but not in methamphetamine-treated mice.
Neurobiol Dis. 33: 459-66. -
Cuadros, M.A. et al. (2006) Specific immunolabeling of brain macrophages and microglial cells in the developing and mature chick central nervous system.
J Histochem Cytochem. 54: 727-38. -
Jiang, H.R. et al. (2001) Total dose and frequency of administration critically affect success of nasal mucosal tolerance induction.
Br J Ophthalmol. 85: 739-44. -
Peng, Y. et al. (2010) L-3-n-butylphthalide improves cognitive impairment and reduces amyloid-beta in a transgenic model of Alzheimer's disease.
J Neurosci. 30: 8180-9. -
Richards, J.G. et al. (2003) PS2APP transgenic mice, coexpressing hPS2mut and hAPPswe, show age-related cognitive deficits associated with discrete brain amyloid deposition and inflammation.
J Neurosci. 23: 8989-9003. -
Li, L. et al. (2008) GRK5 deficiency exaggerates inflammatory changes in TgAPPsw mice.
J Neuroinflammation. 5: 24. -
Rahman, A. et al. (2011) Chronic colitis induces expression of β-defensins in murine intestinal epithelial cells.
Clin Exp Immunol. 163: 123-30. -
Klose, A. et al. (2013) Monocyte/macrophage MMP-14 modulates cell infiltration and T-cell attraction in contact dermatitis but not in murine wound healing.
Am J Pathol. 182: 755-64. -
Ricciardelli, C. et al. (2011) The ADAMTS1 protease gene is required for mammary tumor growth and metastasis.
Am J Pathol. 179: 3075-85. -
Wang, P. et al. (2012) IL-22 signaling contributes to West Nile encephalitis pathogenesis.
PLoS One. 7: e44153. -
Passos, G.F. et al. (2013) The bradykinin B1 receptor regulates Aβ deposition and neuroinflammation in Tg-SwDI mice.
Am J Pathol. 182: 1740-9. -
Medeiros, R. et al. (2011) Loss of muscarinic M1 receptor exacerbates Alzheimer's disease-like pathology and cognitive decline.
Am J Pathol. 179: 980-91. -
Ferrer-Martín, R.M. et al. (2015) Microglial Activation Promotes Cell Survival in Organotypic Cultures of Postnatal Mouse Retinal Explants.
PLoS One. 10 (8): e0135238. -
Tzekov, R. et al. (2016) Sub-Chronic Neuropathological and Biochemical Changes in Mouse Visual System after Repetitive Mild Traumatic Brain Injury.
PLoS One. 11 (4): e0153608. -
Witcher, K.G. et al. (2018) Traumatic brain injury-induced neuronal damage in the somatosensory cortex causes formation of rod-shaped microglia that promote astrogliosis and persistent neuroinflammation.
Glia. 66 (12): 2719-36. -
Boza-Serrano, A. et al. (2019) Galectin-3, a novel endogenous TREM2 ligand, detrimentally regulates inflammatory response in Alzheimer's disease.
Acta Neuropathol. 138 (2): 251-73. -
Da Ros, F. et al. (2017) Targeting Interleukin-1β Protects from Aortic Aneurysms Induced by Disrupted Transforming Growth Factor β Signaling.
Immunity. 47 (5): 959-973.e9. -
Singh, T. et al. (2019) Loss of MafA and MafB expression promotes islet inflammation.
Sci Rep. 9 (1): 9074. -
Tóth, K. et al. (2022) The NKCC1 ion transporter modulates microglial phenotype and inflammatory response to brain injury in a cell-autonomous manner.
PLoS Biol. 20 (1): e3001526.
- Synonyms
- LCA
- RRID
- AB_321729
- UniProt
- P06800
- Entrez Gene
- Ptprc
- GO Terms
- GO:0000187 activation of MAPK activity
- GO:0001915 negative regulation of T cell mediated cytotoxicity
- GO:0001916 positive regulation of T cell mediated cytotoxicity
- GO:0001960 negative regulation of cytokine-mediated signaling pathway
- GO:0002925 positive regulation of humoral immune response mediated by circulating immunoglobulin
- GO:0051726 regulation of cell cycle
- GO:0004725 protein tyrosine phosphatase activity
- GO:0005887 integral to plasma membrane
- GO:0005925 focal adhesion
- View More GO Terms
- GO:0006469 negative regulation of protein kinase activity
- GO:0006470 protein dephosphorylation
- GO:0007159 leukocyte cell-cell adhesion
- GO:0008201 heparin binding
- GO:0009897 external side of plasma membrane
- GO:0019901 protein kinase binding
- GO:0030183 B cell differentiation
- GO:0030890 positive regulation of B cell proliferation
- GO:0031953 negative regulation of protein autophosphorylation
- GO:0034113 heterotypic cell-cell adhesion
- GO:0042098 T cell proliferation
- GO:0042100 B cell proliferation
- GO:0043065 positive regulation of apoptosis
- GO:0043395 heparan sulfate proteoglycan binding
- GO:0043410 positive regulation of MAPKKK cascade
- GO:0045059 positive thymic T cell selection
- GO:0045060 negative thymic T cell selection
- GO:0045121 membrane raft
- GO:0045577 regulation of B cell differentiation
- GO:0045588 positive regulation of gamma-delta T cell differentiation
- GO:0046641 positive regulation of alpha-beta T cell proliferation
- GO:0048304 positive regulation of isotype switching to IgG isotypes
- GO:0050732 negative regulation of peptidyl-tyrosine phosphorylation
- GO:0050852 T cell receptor signaling pathway
- GO:0050853 B cell receptor signaling pathway
- GO:0050855 regulation of B cell receptor signaling pathway
- GO:0050857 positive regulation of antigen receptor-mediated signaling pathway
- GO:0051209 release of sequestered calcium ion into cytosol
- GO:0051607 defense response to virus
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