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Human EDA / Ectodysplasin A Protein (Recombinant DDK) (aa240-391) - LS-G3939

Catalog Size Price
LS-G3939-10 10 µg Unavailable

Most Popular EDA / Ectodysplasin A Proteins

Human EDA / Ectodysplasin A Protein (Recombinant DDK) (aa240-391) - LS-G3939
E. coli Expression System
Purified / Lyophilized / Endotoxin Level: Less than 0.1 EU/µg protein (determined by LAL method).
Mouse EDA / Ectodysplasin A Protein (Recombinant His) (aa141-378) - LS-G14926
E. coli Expression System
Purified / Lyophilized
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human EDA / Ectodysplasin A Protein (Recombinant 8His,N-terminus) (Glu63-Ser391) - LS-G26698
Human HEK 293 Cells
Human EDA / Ectodysplasin A Protein (Recombinant 6His,N-terminus) (Glu63-Ser391) - LS-G26843
Human HEK 293 Cells
Human EDA / Ectodysplasin A Protein (Recombinant Myc + DDK) - LS-G65497
Human HEK 293 Cells
230 AA
Myc + DDK
Purified recombinant protein EDA was analyzed by SDS-PAGE gel and Coomassie Blue Staining

100% Guaranteed
Recombinant Protein
EDA / Ectodysplasin A
~19kDa (SDS-PAGE)
The extracellular domain of human EDA-A1 (aa 240-391) is fused at the N-terminus to a FLAG®-tag.
aa 240-391
E. coli
E. coli
Greater than 95% by SDS-PAGE
Not Tested
Less than 0.1 EU/µg protein (determined by LAL method).
Lyophilized from PBS.
Reconstitute with 100 µl sterile water.
Store lyophilized at -20°C for at least 6 months. Once reconstituted store at 4°C for immediate use.
For research use only.

About EDA / Ectodysplasin A

Q92838 NM_001399 NP_001390.1

EDA Protein, ECTD1 Protein, Ectodermal dysplasia protein Protein, Ectodysplasin-A Protein, ED1 Protein, ED1-A1 Protein, Ectodysplasin A Protein, EDA protein Protein, EDA1 Protein, EDA2 Protein, Hed Protein, HED1 Protein, ODT1 Protein, STHAGX1 Protein, XHED Protein, XLHED Protein, ED1-A2 Protein, Oligodontia 1 Protein

EDA / ED1 is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia.

Requested From: 
Date Requested: 6/21/2018

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