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Recombinant Human TEM7/PLXDC1 Protein (His Tag)

Uniprot : Q8IUK5
  • Cat.No.:PKSH032908

  • Expression host: HEK293 Cells

To Purchase PKSH032908

Size:
  • 10μg
  • 50μg
Price: $129
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Description

Synonyms Plexin Domain-Containing Protein 1;Tumor Endothelial Marker 3;Tumor Endothelial Marker 7;PLXDC1;TEM3;TEM7
Species Human
Expression_host HEK293 Cells
Sequence Leu19-Thr426
Accession AAH36059.1
Mol_Mass 46.5 kDa
AP_Mol_Mass 60-90 kDa
Tag C-His

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, 5% Threhalose, 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 manu
Reconstitution Please refer to the printed manual for detailed information.

Background

Plexin Domain-Containing Protein 1 (PLXDC1) is a single-pass type I membrane protein that belongs to the plexin family. Secreted PLXDC1 is localized predominantly at the tight junctions of vascular endothelial cells and to a lesser extent at the luminal surface of vascular endothelial cells. PLXDC1 is expressed in fibrovascular membrane with increased expression in individuals with proliferative diabetic retinopathy. It can detect in endothelial cells from colorectal cancer, and in endothelial cells from primary cancers of the lung, liver, pancreas, breast and brain. PLXDC1 interacts with NID1 and may also interact with CTTN. It plays a important role in endothelial cell capillary morphogenesis, the proliferation and maintenance of neovascular endothelial cells in the formation of fibrovascular membranes (FVMs).

Citations

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