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RANK/TNFRSF11A Protein, Human, Recombinant (mFc)

TargetMol | SPR
Catalog No. TMPY-05514 Copy Product Info
RANK/TNFRSF11A Protein, Human, Recombinant (mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 46.5 kDa and the accession number is Q9Y6Q6-3.

RANK/TNFRSF11A Protein, Human, Recombinant (mFc)

Catalog No. TMPY-05514
Copy Product Info
TargetMol | SPR

RANK/TNFRSF11A Protein, Human, Recombinant (mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 46.5 kDa and the accession number is Q9Y6Q6-3.

RANK/TNFRSF11A Protein, Human, Recombinant (mFc)
Pack SizePriceUSA StockGlobal StockQuantity
5 μg$687-10 days7-10 days
10 μg$1087-10 days7-10 days
20 μg$1787-10 days7-10 days
50 μg$3597-10 days7-10 days
100 μg$6967-10 days7-10 days
200 μg$1,0607-10 days7-10 days
500 μg$2,2307-10 days7-10 days
1 mg$4,5307-10 days7-10 days
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For In stock only · Estimated delivery:USA Stock (1-2 days) Global Stock (5-7 days)
For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Information

Biological Activity
Recombinant Human TNFRSF11A Protein (Fc Tag) (Cat#TMPY-05514) captured on CM5 chip via Anti-Mouse antibodies surface, can bind Recombinant Human RANKL/OPGL/TNFSF11/CD254 Protein (Cat#TMPY-03364) with an affinity constant of 0.447 nM as determined in an SPR assay (Biacore 8K) (Routinely tested).
Description
RANK/TNFRSF11A Protein, Human, Recombinant (mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 46.5 kDa and the accession number is Q9Y6Q6-3.
Species
Human
Expression System
HEK293 Cells
TagC-mFc
Accession NumberQ9Y6Q6-3
Synonyms
tumor necrosis factor receptor superfamily member 11a,TRANCER,TNFRSF11A,RANK,PDB2,OSTS,OPTB7,OFE,ODFR,LOH18CR1,FEO,CD265
Construction
A DNA sequence encoding the human TNFRSF11A (NP_001257879.1) (Met1-Pro212) was expressed with the Fc region of mouse IgG2a at the C-terminus. Predicted N terminal: Ile 30
Protein Purity
> 95 % as determined by SDS-PAGE.
Molecular Weight46.5 kDa (predicted)
Endotoxin< 1.0 EU/μg of the protein as determined by the LAL method.
FormulationLyophilized from a solution filtered through a 0.22 μm filter, containing PBS, pH 7.4. Typically, a mixture containing 5% to 8% trehalose, mannitol, and 0.01% Tween 80 is incorporated as a protective agent before lyophilization.
Reconstitution
A Certificate of Analysis (CoA) containing reconstitution instructions is included with the products. Please refer to the CoA for detailed information.
Stability & Storage
It is recommended to store recombinant proteins at -20°C to -80°C for future use. Lyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, the solution can be stored at -20°C to -80°C for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.
ShippingIn general, lyophilized powders are shipped with blue ice, while solutions are shipped with dry ice.
Research Background
TNFRSF11A is a member of the TNF-receptor superfamily. In mouse, it is also known as CD265. TNFRSF11A contains 4 TNFR-Cys repeats and is widely expressed with high levels in skeletal muscle, thymus, liver, colon, small intestine and adrenal gland. It is an essential mediator for osteoclast and lymph node development. TNFRSF11A and its ligand are important regulators of the interaction between T cells and dendritic cells. It can interact with various TRAF family proteins, through which this receptor induces the activation of NF-kappa B and MAPK8/JNK. Defects in TNFRSF11A can cause familial expansile osteolysis (FEO). FEO is a rare autosomal dominant bone disorder characterized by focal areas of increased bone remodeling. Defects in TNFRSF11A also can cause Paget disease of bone type 2 (PDB2). PDB2 is a bone-remodeling disorder with clinical similarities to FEO. Defects in TNFRSF11A are the cause of osteopetrosis autosomal recessive type 7 which characterized by abnormally dense bone, due to defective resorption of immature bone.

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