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Anti-EDA / Ectodysplasin A Antibody (Extracellular Domain, clone 174817, Biotin) LS-C36220


Wt. Vol. Conc. Price
100 µg 100 µl - Unavailable

Most Popular EDA / Ectodysplasin A Antibodies

Anti-EDA / Ectodysplasin A Antibody (aa47-76) LS-C99995
Rabbit Polyclonal to Human EDA / Ectodysplasin A
IHC - Paraffin, Western blot, Flow Cytometry
Immunohistochemistry Image
Anti-EDA / Ectodysplasin A Antibody (aa252-301) LS-C102110
Rabbit Polyclonal (IgG) to Human EDA / Ectodysplasin A
Human, Monkey, Mouse, Rat, Bat, Bovine, Dog, Goat, Guinea pig, Horse, Pig, Rabbit, Chicken
Western blot
Western blot Image
Anti-EDA / Ectodysplasin A Antibody LS-C332282
Rabbit Polyclonal (IgG) to Human EDA / Ectodysplasin A
Human, Mouse, Rat
IHC, Western blot
Western blot Image

100% Guaranteed 100% Guaranteed
Mouse Monoclonal [clone 174817] (IgG2b) to Human EDA / Ectodysplasin A
Biotin Conjugated


Human EDA / Ectodysplasin A
Human (tested or 100% immunogen sequence identity)
IgG2b Monoclonal [174817]
Protein G purified


ELISA (0.5 - 2 µg/ml)

Specificity and Use

EDA / Ectodysplasin A antibody was raised against nS0-derived recombinant human EDA-A2 extracellular domain.
Extracellular Domain
Recognizes human EDA-A1 and EDA-A2.
Suitable for use in ELISA. ELISA: 0.5-2 ug/ml. The applications listed have been tested for the unconjugated form of this product. Other forms have not been tested.


100 µl deionized water
For research use only.

About EDA / Ectodysplasin A

Q92838 NM_001399 NP_001390.1

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

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: 3/29/2017

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