LDLRAD3 Belongs to the LDLR family. Contains 3 LDL-receptor class A domains.The low density lipoprotein receptor gene family code for a class of structurally closely related cell surface receptors that fulfill diverse biological functions in different organs, tissues, and cell types. The role that is most commonly associated with this evolutionarily ancient family is cholesterol homeostasis (maintenance of appropriate concentration of cholesterol). In humans, excess cholesterol in the blood is captured by low-density lipoprotein (LDL) and removed in the liver by the endocytosis of the LDL receptor. Recent evidence indicates that the members of the LDL receptor gene family are active in the cell signalling pathways between specialized cells in many, if not all, multicellular organisms.

Mouse Low-density lipoprotein receptor class A domain-containing protein 3 (LDLRAD3) ELISA Kit employs a two-site sandwich ELISA to quantitate LDLRAD3 in samples. An antibody specific for LDLRAD3 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyLDLRAD3 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for LDLRAD3 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of LDLRAD3 bound in the initial step. The color development is stopped and the intensity of the color is measured.

Mouse Low-density lipoprotein receptor class A domain-containing protein 3 (LDLRAD3) ELISA Kit listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

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