RANKL (TNFSF11) (287-304) Rabbit Polyclonal Antibody
Product Data | |
Application | ELISA |
---|---|
Recommended Dilution | ELISA. |
Reactivity | Human |
Antibody Host | Rabbit |
Isotype | IgG |
Clonality | Polyclonal |
Immunogen | Human sRANKL synthetic Peptide (EEISIEVSNPSLLDPDQD) |
Specificity | Recognizes Human sRANKL (soluble form). Other species not tested. |
Buffer | 50 mM TRIS pH 7.4 State: Purified State: Lyophilized purified IgG fraction from Serum |
Reconstitution Method | Restore in aqua bidest to 1 mg/ml |
Purification | Protein G Chromatography |
Conjugation | Unconjugated |
Storage | Store lyophilized at 2-8°C for 6 months or at -20°C long term. After reconstitution store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C long term. Avoid repeated freezing and thawing. |
Stability | Shelf life: one year from despatch. |
Shipping | Ambient |
Gene Name | tumor necrosis factor superfamily member 11 |
Database Link | |
Background | RANKL is a member of the tumor necrosis factor (TNF) cytokine family which is a ligand for osteoprotegerin and functions as a key factor for osteoclast differentiation and activation. There are three isoforms of RANKL. Human RANKL is a soluble 20 kDa polypeptide, comprising the TNF homologous region of RANKL (176 amino acid residues). This protein was shown to be a dentritic cell survival factor and is involved in the regulation of T cell dependent immune response. T cell activation was reported to induce expression of this gene and lead to an increase of osteoclastogenesis and bone loss. This protein was shown to activate antiapoptotic kinase AKT/PKB through a signaling complex involving SRC kinase and tumor necrosis factor receptor associated factor (TRAF) 6, which indicated that this protein may have a role in the regulation of cell apoptosis. RANKL deficient mice show severe osteoporesis and complete absence of osteoclasts as a result of lack of osteogenesis. |
Synonyms | OPGL, RANK Ligand, RANKL, TRANCE, TNFSF11, ODF |
Reference Data | |
Protein Families | Druggable Genome, Transmembrane |
Protein Pathways | Cytokine-cytokine receptor interaction |
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