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The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Congenital heart disease 5 protein; Guided entry of tail-anchored proteins factor 1; Tail-anchored protein insertion receptor WRB; Tryptophan-rich basic protein; tryptophan-rich protein
Gene Aliases: 5530402J05Rik; C030018G21Rik; CHD5; GET1; WRB
UniProt ID: (Human) O00258, (Rat) Q6P6S5, (Mouse) Q8K0D7
Entrez Gene ID: (Human) 7485, (Rat) 288233, (Mouse) 71446
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