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查看说明书Recombinant Human LR3 Insulin-Like Growth Factor I/LR3-IGF-1 Protein(MG)
Cat#:TP04703应用：Positive Control; Immunogen; SDS-PAGE; WB
| Product Name: | LRP5 Rabbit pAb |
| Cat No.: | DPA01489 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,IP |
| Recommended Dilution: | WB: 1:1000 IP: 1:20 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | Recombinant protein of human LRP5 |
| Calculated Molecular Weight: | 179 kDa |
| Observed Molecular Weight: | 200 kDa |
| GenBank Accession Number: | O75197 |
| Gene ID (NCBI): | 4041 |
| Synonyms: | HBM; LR3; OPS; EVR1; EVR4; LRP7; OPPG; BMND1; LRP-5; LRP-7; OPTA1; PCLD4; VBCH2 |
| Background: | This gene encodes a transmembrane low-density lipoprotein receptor that binds and internalizes ligands in the process of receptor-mediated endocytosis. This protein also acts as a co-receptor with Frizzled protein family members for transducing signals by Wnt proteins and was originally cloned on the basis of its association with type 1 diabetes mellitus in humans. This protein plays a key role in skeletal homeostasis and many bone density related diseases are caused by mutations in this gene. Mutations in this gene also cause familial exudative vitreoretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014] |
| Category: | Primary Ab |
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