The scavenger receptor class A (SR-A), also known as Macrophage Scavenger receptor types I and II (MSR1) or CD204, are members of the class A macrophage scavenger receptor family. These proteins bind large quantities of modified lipoproteins and promote endocytosis. SR-A plays a crucial role in lipid metabolism by mediating the uptake of modified LDL, which is significant for understanding atherosclerosis and other lipid-related diseases. SR-A expression occurs predominantly in the liver, placenta, and brain. Upregulation of SR-A in infiltrating myeloid cells may mediate clearance of specific damage signals in response to tissue injury, including ischemic stroke. SR-A germline mutations are also associated with increased prostate cancer susceptibility in some patient cohorts. SR-A contributes to various macrophage-associated pathological processes, including atherosclerosis and Alzheimer′s disease, as well as host defense and cellular adhesion.
Clone
MD405
Isotype
IgG2a/κ
Host species
Mouse
Species Reactivity
Human
Cellular Localization
Cytoplasm
Positive Control
Liver, placenta, thymus, spleen, colon
Applications
IHC, ELISA, IF, IP, WB
Intended Use
Research Use Only
![CD204/MSR1/SR-A [MD405]](https://medaysis.com/wp-content/uploads/2025/09/CD204-MSR1-SR-A-MD405-MC0664_human-placenta-e1759270621115.jpg)