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Recombinant Mouse EDA2R/TNFRSF27 Protein (Fc Tag)

Uniprot : Q8BX35
  • Cat.No.:PKSM041342

  • Expression host: HEK293 Cells

To Purchase PKSM041342

Size:
  • 10μg
  • 50μg
Price: $92
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Description

Synonyms Ectodysplasin A2 receptor;EDA-A2 receptor;EDA-A2R;Tumor necrosis factor receptor superfamily member XEDAR;Tumor necrosis factor receptor superfamily member 27;X-linked ectodysplasin-A2 receptor;EDAA2R;TNFRSF27;XEDAR;EDAR2
Species Mouse
Expression_host HEK293 Cells
Sequence Met1-Thr138
Accession BAC28879
Mol_Mass 42.5 kDa
AP_Mol_Mass 50-60 kDa
Tag C-Fc

Properties

Purity > 95 % as determined by reducing SDS-PAGE.
Endotoxin level < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.
Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.

Background

Tumor necrosis factor receptor superfamily member 27, also known as XEDAR and EDA2R, is a type III transmembrane protein of the TNFR superfamily. EDA2R consists of extracellular domain (ECD) with 3 cysteine-rich repeats and a single transmembrane domain but lacks an N-terminal signal peptide. EDA2R is widely expressed, notably in embryonic basal epidermal cells and maturing hair follicles. Even though it does not contain a cytoplasmic death domain, EDA2R can associate with Fas and induce EDA-A2 dependent apoptosis. Its transcription is directly induced by p53, and it mediated cell death is p53 dependent. it is down-regulated in breast, colon, and lung cancers, particularly in cases with p53 mutations. It also plays a role in EDA-A2 induced skeletal muscle degeneration and osteoblast differentiation. Mutations in the EDA gene are associated with the X-linked form of Hypohidrotic Ectodermal Dysplasia (HED), a disease typically characterized by abnormal hair, teeth and sweat glands.

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