EDA Polyclonal Antibody | G-AB-01261
Gentaur Antibodies
- SKU:
- G-AB-01261
- Availability:
- 3 to 5 Working Days
- Host:
- Rabbit
- Reactivity:
- Human, Mouse
EDA Polyclonal Antibody | G-AB-01261 | Gentaur Antibodies
Overview: 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.
Category Type: Polyclonal Antibody
Research Areas: Developmental Biology, Signal Transduction, Stem Cells
Synonyms: 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
Reactivity: Human, Mouse
Host: Rabbit
Isotype: IgG
Gene ID:
Accession #: NP_001390
Clonality: Polyclonal
Immunogen: Synthetic peptide of human EDA
Clone #:
Conjugation: Unconjugated
Swissprot: Q92838
Santa Cruz: sc-18927/sc-18925/sc-130746
Calculated MW: 49 kDa
Observed MW:
Concentration: 0.2 mg/mL
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Application: WB, IHC, ELISA
Dilution: WB 1:500-1:2000, IHC 1:25-1:100
Storage: Store at -20°C. Avoid freeze / thaw cycles.