NKX2.5 Polyclonal / Biotin /
Product Details
Description | Human NKX2.5 Biotinylated Antibody | |
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Conjugate | Biotin | |
Clone | ||
Target Species | Human | |
Applications | WB, IHC | |
Supplier | R&D Systems | |
Catalog # | Sign in to view product details, citations, and spectra | |
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About NKX2.5
This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
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285 NKX2.5 antibodies from over 18 suppliers available with over 27 conjugates.