The spleen cells from mouse, immunized with recombinant protein of human type ISR-A, were fused with mouse NS-1 myeloma cells. The hybridoma cell line withpositive reaction was grown in ascitic fluid of BALB/c mouse, from which theantibody was purified by Protein G affinity chromatography.
Immunogen
recombinant protein of human type I SR-A
Clone
SRA-E5
Isotype
IgG1
Application Notes
Working dilution for immunohistochemistry: 10ug/ml , for immunoblotting : 2ug/mlAntigen retrieval (microwave 10 min , 0.01M citrate buffer, ph2.0) is recommended for paraffin sections.
Restrictions
For Research Use only
Concentration
0.25 mg/ml
Buffer
PBS (containing 2% Block Ace as a stabilizer, 0.1% Proclin as a bacteriostat)
Preservative
ProClin
Storage
-20 °C
Target
MSRA
(Macrophage Scavenger Receptor A (MSRA))
Alternative Name
Macrophage Scavenger Receptor A(MSR-A:CD204)
Background
Macrophage scavenger receptor (MSR-A: CD204) was identified in the search for the receptor molecules thatare implicated in the pathological deposition of cholesterol during atherogenesis through receptor-mediateduptake of modified low density lipoproteins (LDL).MSR-As possess a wide range of ligand-binding specificities and recognize a variety of molecules such asmodified LDL including acetylated LDL, oxidized LDL, advanced glycation end products (AGE),polyribonucleotides such as poly G and poly I and bacterial surface lipids including lipopolysaccharide andlipoteicoic acid.This antidody was produced from the mouse immunized with recombinant protein of human type IMSR-A ,and has been proved to be useful for the immunoblotting and immunohistochemistry.This antibody is useful tools for the study of MSR in atherogenesis and various other pathological conditionsin humans and animal species.