Osteoprotegerin polyclonal, anti-human, mouse, rat, bovine, horse, pig
€422.00
In stock
SKU
250800
Catalog Nr.: 250800
Size: 0.1 mg
Isotype: Rabbit Ig
Applications: E, WB, IHC
Datasheet
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Size: 0.1 mg
Isotype: Rabbit Ig
Applications: E, WB, IHC
Datasheet
Request Information
Protein Family: Cellular Antigens, Receptors and Channels
Pathway and Disease: Development and Behavior, Signaling Molecules and Interaction
Description:
Osteoprotegerin (OPG) acts as a decoy receptor for RANKL by neutralizing its function in osteoclastogenesis. OPG inhibits osteoclast activation and promotes osteoclast apoptosis in vitro. OPG is up-regulated by increasing calcium concentration and estrogens. Defects in OPG are the cause of juvenile Paget disease, which is characterized by rapid bone remodeling leading to deformities, fractures ans osteopenia.
Alternate Names: Tumor necrosis factor receptor superfamily member 11B, Osteoprotegerin, Osteoclastogenesis inhibitory factor, TNFRSF11B, OCIF, OPG
Application Notes: E: 1:500-1:1,000; WB: 1:200-1:500; IHC: 1:200-1:500
Accession No.: O00300
Antigen: KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human osteoprotegerin.
Format: Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4, 25% glycerol, 1 mg/ml BSA with 0.09% sodium azide. Antibody was purified by Protein-A affinity chromatography.
Storage:
Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment.
Product Citations:
[1] Ray S et al. 2017. Biomaterials. 157: 1-16. PMID 29216500.
[2] Ray S et al. 2016. Injury. Suppl 1:S52-61. PMID 26768293.
[3] Thormann U et al. 2013. Biomaterials. PMID 23906515.
[4] Fradet A et al. 2011. Cancer Research. 71(17): 5728-5738. PMID 21734015.
[5] Fradet A et al. 2013. PLoS ONE. 8(9):e75092. PMID 24069383.
Pathway and Disease: Development and Behavior, Signaling Molecules and Interaction
Description:
Osteoprotegerin (OPG) acts as a decoy receptor for RANKL by neutralizing its function in osteoclastogenesis. OPG inhibits osteoclast activation and promotes osteoclast apoptosis in vitro. OPG is up-regulated by increasing calcium concentration and estrogens. Defects in OPG are the cause of juvenile Paget disease, which is characterized by rapid bone remodeling leading to deformities, fractures ans osteopenia.
Alternate Names: Tumor necrosis factor receptor superfamily member 11B, Osteoprotegerin, Osteoclastogenesis inhibitory factor, TNFRSF11B, OCIF, OPG
Application Notes: E: 1:500-1:1,000; WB: 1:200-1:500; IHC: 1:200-1:500
Accession No.: O00300
Antigen: KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human osteoprotegerin.
Format: Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4, 25% glycerol, 1 mg/ml BSA with 0.09% sodium azide. Antibody was purified by Protein-A affinity chromatography.
Storage:
Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment.
Product Citations:
[1] Ray S et al. 2017. Biomaterials. 157: 1-16. PMID 29216500.
[2] Ray S et al. 2016. Injury. Suppl 1:S52-61. PMID 26768293.
[3] Thormann U et al. 2013. Biomaterials. PMID 23906515.
[4] Fradet A et al. 2011. Cancer Research. 71(17): 5728-5738. PMID 21734015.
[5] Fradet A et al. 2013. PLoS ONE. 8(9):e75092. PMID 24069383.
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