|Tested species reactivity||Hamster, Human, Mink, Mouse, Rodent, Rat|
|Published species reactivity||Hamster|
|Host / Isotype||Goat / IgG|
|Immunogen||Synthetic peptide corresponding to the C-terminal residues 400-509 of mouse SR-BI.|
|Purification||Antigen affinity chromatography|
|Storage buffer||tris citrate, pH 7-8|
|Contains||0.09% sodium azide|
|Storage Conditions||4° C, do not freeze|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||Assay-Dependent|
|Immunohistochemistry (Paraffin) (IHC (P))||Assay-Dependent|
|Western Blot (WB)||1:500|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
|Western Blot (WB)||See 1 publications below|
Suggested positive control: mouse liver lysate or protein.
High density lipoproteins (HDLs) play a critical role in cholesterol metabolism and their plasma concentrations are inversely correlated with risk for atherosclerosis. The SR-BI binds HDLs and mediates selective uptake of HDL cholesteryl ester. SR-BI binds HDL with high affinity, is expressed primarily in liver and nonplacental steroidgenic tissues, and mediates selective cholesterol uptake by a distinct mechanism. In mice, it seems that SR-BI plays a key role in determining the levels of plasma lipoprotein cholesterol and the accumulation of cholesterol stores in the adrenal gland.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Omega 3 fatty acids promote macrophage reverse cholesterol transport in hamster fed high fat diet.
PA1-16803 was used in western blot to study macrophage reverse cholesterol transport in hamsters fed a high fat diet and the effect of omega-3 fatty acid supplementation
|Kasbi Chadli F,Nazih H,Krempf M,Nguyen P,Ouguerram K||PloS one (8:null)||2013|