Anti-Human/Mouse EDA Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12176
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human EDA
Specificity Not abundant; expressed in specific cell types of ectodermal (but not mesodermal) origin of keratinocytes, hair follicles, sweat glands. Also in adult heart, liver, muscle, pancreas, prostate, fetal liver, uterus, small intestine and umbilical chord.
Isotype IgG
Reacitivity Human,Mouse
Clone
Uniprot Q92838
Concentration 0.8 mg/mL
Dilution IHC 1:50-1:200
Formulation
Application IHC,ELISA
Other Names 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
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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