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Invitrogen™ EDA Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA596219
Description
Positive Samples: A-549, HepG2, BxPC-3, Mouse liver; Cellular Location: Cell membrane, Single-pass type II membrane protein Immunogen sequence: LELRSELRRE RGAESRLGGS GTPGTSGTLS SLGGLDPDSP ITSHLGQPSP KQQPLEPGEA ALHSDSQDGH QMALLNFFFP DEKPYSEEES RRVRRNKRSK SNEGADGPVK NKKKGKKAGP P.
EDA is a type II membrane protein that can be cleaved by furin to produce a secreted form. This 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 the gene for EDA are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia.
Specifications
EDA | |
Polyclonal | |
Unconjugated | |
EDA | |
ECTD1; ectodermal dysplasia 1, anhidrotic; ectodermal dysplasia protein; Ectodysplasin; Ectodysplasin 1, isoform A2; ectodysplasin A; ectodysplasin-1; Ectodysplasin-A; Ectodysplasin-A, membrane form; Ectodysplasin-A, secreted form; Ed1; ED1-A1; ED1-A2; EDA; EDA 1; EDA protein; EDA protein homolog; EDA1; EDA2; Eda-A1; EDA-A2; HED; HED1; nackt; nkt; ODT1; oligodontia 1; RGD1563178; si:ch73-223d24.5; STHAGX1; Ta; tabby; Tabby protein; TNLG7C; tumor necrosis factor ligand 7C; XHED; XLHED; X-linked anhidroitic ectodermal dysplasia protein | |
Rabbit | |
Affinity chromatography | |
RUO | |
13607, 1896, 302424 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
ELISA, Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
0.43 mg/mL | |
PBS with 50% glycerol and 0.05% ProClin 300; pH 7.3 | |
O54693, Q92838 | |
EDA | |
A synthetic peptide corresponding to a sequence within amino acids 62-182 of human EDA (NP_0013901). | |
100 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
Safety and Handling
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