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LRP2 Polyclonal Antibody Store at -20°C

SKU: E-AB-12482-200

  • $ 55995


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LRP2 Polyclonal Antibody Store at -20°C

 

SKU # E-AB-12482
Reactivity Human, Mouse, Rat
Host Rabbit
Applications IHC

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse, Rat
Applications IHC
Clonality Polyclonal
Immunogen Synthetic peptide of human LRP2
Abbre LRP2
Synonyms Calcium sensor protein,  DBS,  Glycoprotein 330,  Heymann nephritis antigen homolog,  LRP-2,  LRP2,  Low-density lipoprotein receptor-related protein 2,  Lrp2,  Megalin,  gp330
Swissprot
Cellular Localization Membrane. Membrane>coated pit.
Concentration 0.5 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Cardiovascular,  Metabolism,  Developmental Biology,  Stem Cells
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
IHC  1:50-1:200

 

Background

The protein encoded by this gene, low density lipoprotein-related protein 2 (LRP2) or megalin, is a multi-ligand endocytic receptor that is expressed in many different tissues but primarily in absorptive epithilial tissues such as the kidney. This glycoprotein has a large amino-terminal extracellular domain, a single transmembrane domain, and a short carboxy-terminal cytoplasmic tail. The extracellular ligand-binding-domains bind diverse macromolecules including albumin, apolipoproteins B and E, and lipoprotein lipase. The LRP2 protein is critical for the reuptake of numerous ligands, including lipoproteins, sterols, vitamin-binding proteins, and hormones. This protein also has a role in cell-signaling; extracellular ligands include parathyroid horomones and the morphogen sonic hedgehog while cytosolic ligands include MAP kinase scaffold proteins and JNK interacting proteins. Recycling of this membrane receptor is regulated by phosphorylation of its cytoplasmic domain. Mutations in this gene cause Donnai-Barrow syndrome (DBS) and facio-oculoacoustico-renal syndrome (FOAR).