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MSR1 encodes the class A macrophage scavenger receptors, which include three different types (1, 2, 3) generated by alternative splicing of MSR1. 再加上，我们可以发Macrophage Scavenger Receptor 1 试剂盒 (22) 和 Macrophage Scavenger Receptor 1 蛋白 (15)和数多这个蛋白质的别的产品。
Showing 10 out of 234 products:
Mouse (Murine) Monoclonal Macrophage Scavenger Receptor 1 Primary Antibody for EIA, FACS - ABIN181780
de Villiers, Fraser, Hughes, Doyle, Gordon: Macrophage-colony-stimulating factor selectively enhances macrophage scavenger receptor expression and function. in The Journal of experimental medicine 1994
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Mouse (Murine) Monoclonal Macrophage Scavenger Receptor 1 Primary Antibody for FACS - ABIN319577
Hughes, Fraser, Gordon: Murine macrophage scavenger receptor: in vivo expression and function as receptor for macrophage adhesion in lymphoid and non-lymphoid organs. in European journal of immunology 1995
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Mouse (Murine) Monoclonal Macrophage Scavenger Receptor 1 Primary Antibody for FACS - ABIN181781
Bell, Lopez-Gonzalez, Lawson, Hughes, Fraser, Gordon, Perry: Upregulation of the macrophage scavenger receptor in response to different forms of injury in the CNS. in Journal of neurocytology 1995
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Mouse (Murine) Monoclonal Macrophage Scavenger Receptor 1 Primary Antibody for EIA, Func - ABIN181779
Daugherty, Whitman, Block, Rateri: Polymorphism of class A scavenger receptors in C57BL/6 mice. in Journal of lipid research 2001
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Mouse (Murine) Monoclonal Macrophage Scavenger Receptor 1 Primary Antibody for FACS - ABIN181777
Fraser, Hughes, Gordon: Divalent cation-independent macrophage adhesion inhibited by monoclonal antibody to murine scavenger receptor. in Nature 1993
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Human Polyclonal Macrophage Scavenger Receptor 1 Primary Antibody for ICC, IHC (fro) - ABIN314198
Piccolo, Vetrini, Mithbaokar, Grove, Bertin, Palmer, Ng, Brunetti-Pierri: SR-A and SREC-I are Kupffer and endothelial cell receptors for helper-dependent adenoviral vectors. in Molecular therapy : the journal of the American Society of Gene Therapy 2013
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Human Monoclonal Macrophage Scavenger Receptor 1 Primary Antibody for FACS, WB - ABIN4900486
Hongo, Watanabe, Arita, Kanome, Kageyama, Shioda, Miyazaki: Leptin modulates ACAT1 expression and cholesterol efflux from human macrophages. in American journal of physiology. Endocrinology and metabolism 2009
Human Monoclonal Macrophage Scavenger Receptor 1 Primary Antibody for FACS - ABIN4897783
Tran, Ahern, Hodge, Holt, Dean, Reynolds, Hodge: Oxidative stress decreases functional airway mannose binding lectin in COPD. in PLoS ONE 2014
Human Polyclonal Macrophage Scavenger Receptor 1 Primary Antibody for WB - ABIN1537159
Chen, Li, Zhu: AMP-activated protein kinase attenuates oxLDL uptake in macrophages through PP2A/NF-?B/LOX-1 pathway. in Vascular pharmacology 2015
Mouse (Murine) Monoclonal Macrophage Scavenger Receptor 1 Primary Antibody for FACS - ABIN4897805
Cavnar, Zeng, Kim, Sorenson, Ocuin, Balachandran, Seifert, Greer, Popow, Crawley, Cohen, Green, Rossi, Besmer, Antonescu, DeMatteo: KIT oncogene inhibition drives intratumoral macrophage M2 polarization. in The Journal of experimental medicine 2013
SR-A1 suppresses lung cancer metastasis by downregulating SAA1 (显示 SAA1 抗体) production in tumor-associated macrophages (TAM (显示 CCNA1 抗体)).
PTX2 (显示 APCS 抗体) was identified PTX2 (显示 APCS 抗体) as a novel partner for FX, and both proteins cooperated to prevent their SR-AI-mediated uptake by macrophages.
we found that higher percentages of circulating CD14 (显示 NDUFA2 抗体)+CD204+, CD14 (显示 NDUFA2 抗体)+CD163 (显示 CD163 抗体)+CD204+ M2-like monocytes were significantly associated with TNM (显示 ODZ1 抗体) stage, lymph node metastasis, and histological differentiation.
Identifying N-linked glycan moiety and motifs in the cysteine-rich domain critical for N-glycosylation and intracellular trafficking of SR-AI and MARCO (显示 MARCO 抗体).
The P275A Polymorphism in the Macrophage Scavenger Receptor 1 Gene is not associated with Prostate Cancer Risk.
Cyr61 (显示 CYR61 抗体) promotes CD204 expression and the migration of macrophages via MEK (显示 MAP2K1 抗体)/ERK (显示 EPHB2 抗体) pathway in esophageal squamous cell carcinoma
miR (显示 MLXIP 抗体)-29a promotes scavenger receptor A expression by targeting QKI (显示 QKI 抗体) during monocyte-macrophage differentiation.
Heptapeptide XD4 activates the class A scavenger receptor (SR-A) on the glia by increasing the binding of Abeta (显示 APP 抗体) to SR-A, thereby promoting glial phagocytosis of Abeta (显示 APP 抗体) oligomer in microglia.
The truncating variant Arg293X in the gene encoding SRA (显示 SRA1 抗体)-I/II was associated with reduced lung function and with increased risk of COPD (显示 ARCN1 抗体) among men, as well as among alpha1-antitrypsin MZ and superoxide dismutase (显示 SOD1 抗体)-3 E1I1 heterozygotes.
monomeric collagen type I via CD204 induces phospho-Akt (显示 AKT1 抗体) expression shifting alveolar macrophages to the profibrotic M2 type. Innate immune responses induced by collagen monomers might perpetuate pulmonary fibrosis.
Data (including data from studies conducted in cells from knockout mice) suggest that signaling via Lpar1 (显示 LPAR1 抗体), Cd14 (显示 CD14 抗体), and Scara1 mediates uptake of oxidized LDL by macrophages leading to foam cell formation; lysophosphatidic acid (LPA) induces expression of Cd14 (显示 CD14 抗体) and Scara1 in macrophages. (Lpar1 (显示 LPAR1 抗体) = LPA receptor 1 (显示 LPAR1 抗体); Cd14 (显示 CD14 抗体) = monocyte differentiation antigen CD14 (显示 CD14 抗体); Scara1 = scavenger receptor class A type I)
Common damage-associated molecular patterns (DAMPs) were internalized through the class A scavenger receptors MSR1 and MARCO (显示 MARCO 抗体) in vitro. In ischemic murine brain, DAMP (显示 AMPH 抗体) internalization was largely mediated by MSR1. Combined deficiency for Msr1 and Marco (显示 MARCO 抗体) in infiltrating myeloid cells caused impaired clearance of DAMPs, more severe inflammation, and exacerbated neuronal injury in a murine model of ischemic stroke.
PTX2 (显示 PITX2 抗体) was identified PTX2 (显示 PITX2 抗体) as a novel partner for FX, and both proteins cooperated to prevent their SR-AI-mediated uptake by macrophages.
this study shows that Msr1 functions as co-receptor along with TLRs for HMGB1 (显示 HMGB1 抗体) in M1-type inflammatory macrophages
Our findings demonstrated that ClC-3 (显示 CLCN3 抗体) deficiency inhibits atherosclerotic lesion development, possibly via suppression of JNK (显示 MAPK8 抗体)/p38 MAPK (显示 MAPK14 抗体) dependent SR-A expression and foam cell formation
FAP (显示 FAP 抗体)-cleaved collagen is a substrate for SR-A-dependent macrophage adhesion.
Macrophages regulate FX plasma levels in an SR-AI-dependent manner.
The results of this results reveal that SRA has important clinical implications for TLR-targeted immunotherapeutical strategy in intracerebral hemorrhage.
these findings suggest that SR-A-mediated dsRNA internalization is independent of innate antiviral signaling.
Our findings imply that SR-A may be an important target for improving therapeutic strategies for type 1 diabetes.
This gene encodes the class A macrophage scavenger receptors, which include three different types (1, 2, 3) generated by alternative splicing of this gene. These receptors or isoforms are macrophage-specific trimeric integral membrane glycoproteins and have been implicated in many macrophage-associated physiological and pathological processes including atherosclerosis, Alzheimer's disease, and host defense. The isoforms type 1 and type 2 are functional receptors and are able to mediate the endocytosis of modified low density lipoproteins (LDLs). The isoform type 3 does not internalize modified LDL (acetyl-LDL) despite having the domain shown to mediate this function in the types 1 and 2 isoforms. It has an altered intracellular processing and is trapped within the endoplasmic reticulum, making it unable to perform endocytosis. The isoform type 3 can inhibit the function of isoforms type 1 and type 2 when co-expressed, indicating a dominant negative effect and suggesting a mechanism for regulation of scavenger receptor activity in macrophages.
macrophage scavenger receptor 1
, macrophage scavenger receptor types I and II-like
, macrophage acetylated LDL receptor I and II
, macrophage scavenger receptor type III
, macrophage scavenger receptor types I and II
, scavenger receptor class A member 1
, scavenger receptor class A, member 1
, scavenger receptor type A
, macrophage scavenger receptor type I