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Human EDAR Protein (Met1-Ala187) - LS-G50270

Catalog Size Price
LS-G50270-50 50 µg Unavailable
LS-G50270-100 100 µg Unavailable

Most Popular EDAR Proteins

Human EDAR Protein (Recombinant His) - LS-G3082
E. coli Expression System
445 AA
His
Purified
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human EDAR Protein (Recombinant Human IgG1 Fc) (aa27-183) - LS-G3946
Hamster-Chinese CHO Cells
Human IgG1 Fc
Purified / Lyophilized / Biologically Active / Endotoxin Level: Less than 0.01 EU/µg protein (determined by LAL method).
Mouse EDAR Protein (Recombinant Fc,C-terminus) (Glu27-Ile189) - LS-G40133
Human Human Cells
404 AA
Fc,C-terminus
Purified / Lyophilized / Endotoxin Level: Less than 1.0 EU/µg protein (determined by LAL method).
Human EDAR Protein (Met1-Ile189) - LS-G47544
Human HEK 293 Cells
None
Purified / Lyophilized / Endotoxin Level: Less than 1.0 EU/µg protein (determined by LAL method).
Human EDAR Protein (Met1-Ile189) - LS-G48489
None
Purified / Lyophilized / Endotoxin Level: Less than 1.0 EU/µg protein (determined by LAL method).

100% Guaranteed
LS-G50270
EDAR
Human
Met 1-Ala 187
HEK 293 Cells
Human
None
Greater than 95% by SDS-PAGE
Not Tested
Less than 1.0 EU/µg protein (determined by LAL method).
Lyophilized from sterile PBS, pH 7.4
Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
For research use only.

About EDAR

Q9UNE0 NM_022336 NP_071731.1

EDAR Protein, Ectodysplasin-A receptor Protein, ED1R Protein, EDA-A1 receptor Protein, EDA1R Protein, DL Protein, Downless, mouse, homolog of Protein, ED3 Protein, EDA3 Protein, ECTD10A Protein, ECTD10B Protein, Ectodysplasin A receptor Protein, ED5 Protein, Downless homolog Protein, Ectodermal dysplasia receptor Protein, EDA-A1R Protein, HRM1 Protein

EDAR is a member of the tumor necrosis factor receptor family. The encoded transmembrane protein is a receptor for the soluble ligand ectodysplasin A, and can activate the nuclear factor-kappaB, JNK, and caspase-independent cell death pathways. It is required for the development of hair, teeth, and other ectodermal derivatives. Mutations in this gene result in autosomal dominant and recessive forms of hypohidrotic ectodermal dysplasia.

Requested From: 
Date Requested: 10/17/2017

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