RANKL/TNFSF11 Protein, Human
Based on 11 publication(s) in Google Scholar
RANKL (TNFSF11), a type II transmembrane protein, is receptor activator of NF-κB (RANK) ligand. RANKL is an activator of RANK. When binding to RANK, it induces the differentiation of monocyte/macrophage-lineage cells into osteoclasts and leads to osteoclast precursor maturation. RANKL is critical for osteoclasts maturation, bone modeling, and bone remodeling, as well as the development of lymph nodes (LNs). RANKL/TNFSF11 Protein, Human is a recombinant human RANKL (I140-D317) without any tag, which is produced in E.coli.
- Species: Human
- Source: E. coli
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Storage:Stored at -20°C for 2 years from date of receipt. After reconstitution, it is stable at 4°C for 1 week or -20°C for longer (with carrier protein). It is recommended to freeze aliquots at -20°C or -80°C for extended storage.
Biological Activity
Description
RANKL (TNFSF11), a type II transmembrane protein, is receptor activator of NF-κB (RANK) ligand. RANKL is an activator of RANK. When binding to RANK, it induces the differentiation of monocyte/macrophage-lineage cells into osteoclasts and leads to osteoclast precursor maturation. RANKL is critical for osteoclasts maturation, bone modeling, and bone remodeling, as well as the development of lymph nodes (LNs). RANKL/TNFSF11 Protein, Human is a recombinant human RANKL (I140-D317) without any tag, which is produced in E.coli[1][2].
Background
RANKL (TNFSF11) belongs to TNF family. RANKL is a type II transmembrane protein and is a receptor activator of NF-κB (RANK) ligand. RANKL is an activator of RANK. RANKL binds to RANK and induces the differentiation of monocyte/macrophage-lineage cells into osteoclasts and leads to osteoclast precursor maturation. In bone tissue, RANKL is expressed by osteoblasts, osteocytes and immune cells, especially in osteoblasts and osteocytes[1]. RANKL is also expressed by T cells and increases proliferation and survival of dendritic cells[2].
Human RANKL shares 82.02% and 84.44% common aa identity with mouse and rat respectively. Human RANKL consists of cytoplasmic domain (1-47), helical domain (48-68), and extracellular domain (69-317). The soluble chain (140-317) is released when cleaved by enzymes such as matrix metalloproteinases (MMP3 or 7) and ADAM[1][3].
RANKL is critical for osteoclasts maturation, bone modeling, and bone remodeling, as well as the development of lymph nodes (LNs)[1].
In Vitro
RANKL (human, 0-50 ng/mL, 24 h) stimulates migration of a clear cell RCC cell line, Caki-1[4].
RANKL (human, 24 h) stimulates PAa cell migration and invasion[5].
In Vivo
RANKL (human, 0.4 or 2 mg/kg/day, s.c.) induces high bone turnover and decreases bone volume, density, and strength in C57BL/6J female mice[6].
Verified Bioactivity
1.Immobilized Recombinant Human RANK L at 10 μg/mL (100 μL/well) can bind Recombinant Human RANK (HY-P72484). The ED50 for this effect is <3.23 μg/mL.
2.Immobilized Human RANK/TNFRSF11A at 0.5 μg/mL can bind Biotinylated Human RANKL. The ED50 for this effect is < 15 ng/mL.
MCE Validation Data
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Purity - SDS-PAGE
Purity - SDS-PAGE
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Bioactivity - ELISA
Bioactivity - ELISA
Publications (11)
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Journal Impact Factor
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Most Recent
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Am J Chin Med
Emodin Inhibitsg Hepatocellular Carcinoma Invasion and Migration by Regulating the HDAC4/NF-κB (p65)/CXCL12 Signaling Axis and Suppressing M2 Macrophage Polarization. [Abstract]2026 Apr 25:1-33. PMID: 42036631 -
Biochem Pharmacol
USP10-mediated deubiquitination of NR3C1 regulates bone homeostasis by controlling CST3 expression. [Abstract]2024 Nov:229:116519. PMID: 39236936
RANKL/TNFSF11 Protein, Human purchased from MedChemExpress. Usage Cited in: Biochem Pharmacol. 2024 Nov:229:116519. [Abstract]
RANKL/TNFSF11 Protein, Human (50 ng/mL; 3 days) induced Osteoclastic differentiation in RAW264.7 cells.
RANKL/TNFSF11 Protein, Human purchased from MedChemExpress. Usage Cited in: Biochem Pharmacol. 2024 Nov:229:116519. [Abstract]
RANKL/TNFSF11 Protein, Human (50 ng/mL; 3 days) suppressed NFATC1, CTSK, and MMP9 mRNA expression in RAW264.7 cells.
RANKL/TNFSF11 Protein, Human purchased from MedChemExpress. Usage Cited in: Biochem Pharmacol. 2024 Nov:229:116519. [Abstract]
RANKL/TNFSF11 Protein, Human (50 ng/mL; 5 days) showed downregulation of NR3C1, which impaired osteoclast differentiation in BMDM.
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Regen Ther
Denosumab ameliorates osteoarthritis by protecting cartilage against degradation and modulating subchondral bone remodeling. [Abstract]2024 Mar 26:27:181-190. PMID: 38840731 -
Tissue Cell
Exosomes secreted from M2-polarized macrophages inhibit osteoclast differentiation via CYLD. [Abstract]2025 Apr:93:102645. PMID: 39671756 -
J Invest Surg
Functional Study of the circRNA_0006393/miR-375/IGFBP4 Axis in Fracture Healing Associated with Male Idiopathic Osteoporosis. [Abstract]2025 Dec;38(1):2535522. PMID: 40728000 -
Exp Ther Med
Bioinformatics analysis identification of AKT3 and RAC1 as key genes in postmenopausal osteoporosis. [Abstract]2022 Sep 7;24(5):656. PMID: 36168425 -
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Heliyon
TDO2 deficiency attenuates the hepatic lipid deposition and liver fibrosis in mice with diet-induced non-alcoholic fatty liver disease. [Abstract]2023 Nov 18;9(11):e22464. PMID: 38074859 -
Environ Toxicol
METTL14 represses osteoclast formation to ameliorate osteoporosis via enhancing GPX4 mRNA stability. [Abstract]2023 Sep;38(9):2057-2068. PMID: 37195267 -
Bioengineered
Synergetic protective effect of berberine and ginsenoside Rb1 against tumor necrosis factor alpha-induced inflammation in adipocytes. [Abstract]2021 Dec;12(2):11784-11796. PMID: 34699329
RANKL/TNFSF11 Protein, Human purchased from MedChemExpress. Usage Cited in: Bioengineered. 2021 Dec;12(2):11784-11796. [Abstract]
RANKL/TNFSF11 Protein, Human (100 ng/mL) decreased cell viability in 3T3-L1 cells.
RANKL/TNFSF11 Protein, Human purchased from MedChemExpress. Usage Cited in: Bioengineered. 2021 Dec;12(2):11784-11796. [Abstract]
RANKL/TNFSF11 Protein, Human (100 ng/mL) markedly reversed the effect of TNF-α on IL-6 secretion in 3T3-L1 cells.
RANKL/TNFSF11 Protein, Human purchased from MedChemExpress. Usage Cited in: Bioengineered. 2021 Dec;12(2):11784-11796. [Abstract]
RANKL/TNFSF11 Protein, Human (100 ng/mL) resulted in a higher suppression of Bcl-2 expression and a higher increase in the expression of cleaved caspase-3 compared to the effects of only BBR+Rb1.
RANKL/TNFSF11 Protein, Human purchased from MedChemExpress. Usage Cited in: Bioengineered. 2021 Dec;12(2):11784-11796. [Abstract]
RANKL/TNFSF11 Protein, Human (100 ng/mL) increased the sum of area significantly in 3T3-L1 cells. Adipogenesis was evaluated by performing oil red O staining assay.
RANKL/TNFSF11 Protein, Human purchased from MedChemExpress. Usage Cited in: Bioengineered. 2021 Dec;12(2):11784-11796. [Abstract]
RANKL/TNFSF11 Protein, Human (100 ng/mL) showed the r fluorescence intensity of NF-κB p65 was significantly increased 3T3-L1 cells.
Technical Parameters
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Species Human
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Source E. coli
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Tag Tag Free
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Accession
O14788-1 (I140-D317)
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Molecular Construction
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N-term
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RANKL (I140-D317)
Accession # O14788 -
C-term
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Protein Length
Full Length of TNFSF11, soluble form
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Synonyms
TNFSF11; Tumor Necrosis Factor (Ligand) Superfamily, Member 11; TNF Superfamily Member 11; Receptor Activator Of Nuclear Factor Kappa-B Ligand; TRANCE; TNLG6B; RANKL; Receptor Activator Of Nuclear Factor Kappa B Ligand; OPGL; Tumor Necrosis Factor Ligand
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AA Sequence
IRAEKAMVDGSWLDLAKRSKLEAQPFAHLTINATDIPSGSHKVSLSSWYHDRGWAKISNMTFSNGKLIVNQDGFYYLYANICFRHHETSGDLATEYLQLMVYVTKTSIKIPSSHTLMKGGSTKYWSGNSEFHFYSINVGGFFKLRSGEEISIEVSNPSLLDPDQDATYFGAFKVRDID
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Molecular Weight
Approximately 20 kDa, based on SDS-PAGE under reducing conditions.
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Purity
≥ 90%, as determined by reducing SDS-PAGE.
Product Properties
Lyophilized powder
1.Lyophilized from a 0.22 μm filtered solution of 20 mM Tris-HCl, 150 mM NaCl, pH 8.0.
2.Lyophilized from a 0.22 μm filtered solution of PBS, pH 8.0.
3.Lyophilized from a 0.22 μm filtered solution of PBS, pH 8.0, 8% trehalose.
Please refer to the lot-specific COA for specific buffer information.
Note: For SPR assay, please replace the buffer. Primary amine components (e.g., Tris, imidazole) can affect protein-coupled chips.
<1.0 EU/μg, determined by LAL method.
It is not recommended to reconstitute to a concentration less than 100 μg/mL in ddH2O. For long term storage it is recommended to add a carrier protein (0.1% BSA, 5% HSA, 10% FBS or 5% Trehalose).
Stored at -20°C for 2 years from date of receipt. After reconstitution, it is stable at 4°C for 1 week or -20°C for longer (with carrier protein). It is recommended to freeze aliquots at -20°C or -80°C for extended storage.
Room temperature in continental US; may vary elsewhere.
Documentation
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Data Sheet (264 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
[1]. Ono T, et al. RANKL biology: bone metabolism, the immune system, and beyond. Inflamm Regen. 2020 Feb 7;40:2. [Content Brief]
[2]. Hofbauer LC, et al. Role of receptor activator of nuclear factor-kappaB ligand and osteoprotegerin in bone cell biology. J Mol Med (Berl). 2001 Jun;79(5-6):243-53. [Content Brief]
[3]. Li B, et al. Roles of the RANKL-RANK Axis in Immunity-Implications for Pathogenesis and Treatment of Bone Metastasis. Front Immunol. 2022 Mar 21;13:824117. [Content Brief]
[4]. Tobeiha M, et al. RANKL/RANK/OPG Pathway: A Mechanism Involved in Exercise-Induced Bone Remodeling. Biomed Res Int. 2020 Feb 19;2020:6910312. [Content Brief]
[5]. Mikami S, et al. Increased RANKL expression is related to tumour migration and metastasis of renal cell carcinomas. J Pathol. 2009 Aug;218(4):530-9. [Content Brief]
[6]. Peng X, et al. Differential expression of the RANKL/RANK/OPG system is associated with bone metastasis in human non-small cell lung cancer. PLoS One. 2013;8(3):e58361. [Content Brief]
[7]. Lloyd SA, et al. Soluble RANKL induces high bone turnover and decreases bone volume, density, and strength in mice. Calcif Tissue Int. 2008 May;82(5):361-72. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)