EDA Polyclonal Antibody

SKU: E-AB-12380

Size::120μL

Storage:Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.

Shipping:The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

Exp date:12 months

Category ID_II:Primary Antibodies

Category ID_III:Polyclonal Antibodies

Abbreviation:EDA

Target Synonym:ECTD1;Ectodermal dysplasia 1;anhidrotic;Ectodermal dysplasia protein;Ectodermal dysplasia;anhidrotic (hypohydrotic);Ectodysplasin A;Ectodysplasin A;membrane form;Ectodysplasin A;secreted form;ECTODYSPLASIN A1 ISOFORM;ECTODYSPLASIN A2 ISOFORM;ECTODYSPLASIN;Ectodysplasin-A;ED1 A1;ED1 A2;ED1;ED1 GENE;Eda A1;Eda A2;eda;EDA protein;EDA protein homolog;EDA;EDA1;EDA1 GENE;EDA2;HED;HED1;ODT1;Oligodontia 1;secreted form;STHAGX1;Ta;Tabby;Tabby protein;X linked anhidroitic ectodermal dysplasia protein;XHED;XLHED

Research Areas:Developmental Biology;Signal Transduction;Stem Cells

Conjugation:Unconjugated

Host:Rabbit

Species reactivity:Human;Mouse

Application:WB;IHC

Isotype:IgG

Clonality:Polyclonal

Clone NO.:

UNIProt ID:Q92838

Accession:

Background: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.

Concentration:0.2 mg/mL

Immunogen:Synthetic peptide of human EDA

Buffer:PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method:Affinity purification

Dilution:WB 1:500-1:2000;IHC 1:25-1:100

Calculated MW:49kDa

ObservedMW: