EDA Antibody - middle region - Biotin

Referencia ARP44519_P050-Biotin

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EDA Antibody - middle region : Biotin (ARP44519_P050-Biotin)

Datasheets/ManualsPrintable datasheet for anti-EDA (ARP44519_P050-Biotin) antibody
Product Info
Predicted Species ReactivityHuman, Mouse, Rat, Cow, Dog, Goat, Guinea Pig, Horse, Rabbit
Product FormatLiquid. Purified antibody supplied in 1x PBS buffer.
ClonalityPolyclonal
HostRabbit
ConjugationBiotin
ApplicationWB
Reconstitution and StorageAll conjugated antibodies should be stored in light-protected vials or covered with a light protecting material (i.e. aluminum foil). Conjugated antibodies are stable for at least 12 months at 4C. If longer storage is desired (24 months), conjugates may be diluted with up to 50% glycerol and stored at -20C to -80C. Freezing and thawing conjugated antibodies will compromise enzyme activity as well as antibody binding.
ImmunogenThe immunogen is a synthetic peptide directed towards the middle region of human EDA
PurificationAffinity Purified
Predicted Homology Based on Immunogen SequenceCow: 100%; Dog: 100%; Goat: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 100%
Peptide SequenceSynthetic peptide located within the following region: HLQGQGSAIQVKNDLSGGVLNDWSRITMNPKVFKLHPRSGELEVLVDGTY
Concentration0.5 mg/ml
Blocking PeptideFor anti-EDA (ARP44519_P050-Biotin) antibody is Catalog # AAP44519 (Previous Catalog # AAPP12035)
ReferenceZhao,J., (2008) Br. J. Dermatol. 158 (3), 614-617
Gene SymbolEDA
Gene Full NameEctodysplasin A
Alias SymbolsED1, HED, EDA1, EDA2, HED1, ODT1, XHED, ECTD1, XLHED, ED1-A1, ED1-A2, EDA-A1, EDA-A2, TNLG7C, STHAGX1
NCBI Gene Id1896
Protein NameEctodysplasin-A
Description of TargetEDA is a type II membrane protein that can be cleaved by furin to produce a secreted form. It 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. Several transcript variants encoding many different isoforms have been found for this gene. The protein encoded by this gene 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. Several transcript variants encoding many different isoforms have been found for this gene.
Uniprot IDB7ZLU4
Protein Accession #NP_001005609
Nucleotide Accession #NM_001005609
Protein Size (# AA)389
Molecular Weight41kDa
Protein InteractionsOSTCP1; OSTC; NIPAL3; GIMAP5; SEC22A; LEPROTL1; DOLK; PLN; MAL; EMP3; CYB561; ATP6V0C; EDAR; EDA; EDA2R; FURIN;