Human CD204/MSR1 protein (Recombinant-Active) (N-His) (STJP011918)

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STJP011918-100
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Short Description :Recombinant-Active-Human CD204/MSR1-N-His protein was developed from mammalian cells and has a target region of N-His. For use in research applications.
Applications:ELISA/WB
Host:Mammalian Cells
Note:STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Conjugation:Unconjugated
Dilution Range:Reconstitute in sterile water for a stock solution.
Formulation:Lyophilized from a solution in PBS pH 7.4, 5% Trehalose, 5% Mannitol.
Storage Instruction:Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for one week. Store at-20 to-80°C for twelve months from the date of receipt.
Endotoxin:<0.1 EU/Mu g of the protein by the LAL method.
Immunoreactivity:Measured by its binding ability in a functional ELISA. Immobilised recombinant human CD204/MSR1 at 5 µg/mL (100 µL/well) can bind biotinylated advanced glycation endproducts of bovine serum albumin (AGEBSA) with a linear range of 6-400 ng/mL.
Gene Symbol:MSR1
Gene ID:4481
Uniprot ID:MSRE_HUMAN
Immunogen:Homo sapiens (Human)
Immunogen Region:Lys77-Leu451
Function Membrane glycoproteins implicated in the pathologic deposition of cholesterol in arterial walls during atherogenesis. Two types of receptor subunits exist. These receptors mediate the endocytosis of a diverse group of macromolecules, including modified low density lipoproteins (LDL). Isoform III does not internalize acetylated LDL.
Protein Name Macrophage Scavenger Receptor Types I And Ii
Macrophage Acetylated Ldl Receptor I And Ii
Scavenger Receptor Class A Member 1
Cd Antigen Cd204
Database Links Reactome: R-HSA-3000480
Cellular Localisation Membrane
Single-Pass Type Ii Membrane Protein
Alternative Protein Names Macrophage Scavenger Receptor Types I And Ii protein
Macrophage Acetylated Ldl Receptor I And Ii protein
Scavenger Receptor Class A Member 1 protein
Cd Antigen Cd204 protein
MSR1 protein
SCARA1 protein

Information sourced from Uniprot.org