EDA Polyclonal Antibody

SKU: E-AB-14972

Size: 200μL

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: 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: 0.8 mg/mL

Immunogen: Recombinant protein of human EDA

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

Purification method: Affinity purification

Dilution: IHC 1:50-1:200

Calculated MW:

ObservedMW: