Synthetic peptide from human protein at AA range: 271-320
Storage:
Rabbit
Storage:
-20°C/1 year
Clonality:
Polyclonal
Isotype:
IgG
Concentration:
1 mg/ml
GeneID（Human）:
2138/2140
Human Swiss-Prot No:
Q99502/O95677
Cellular localization:
Cytoplasm . Nucleus . Localizes at sites of DNA damage at double-strand breaks (DSBs). .
Background:
EYA transcriptional coactivator and phosphatase 1(EYA1) Homo sapiens This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2013],
Immunohistochemical analysis of paraffin-embedded Human-kidney, antibody was diluted at 1:100
Immunohistochemical analysis of paraffin-embedded Human-kidney, antibody was diluted at 1:100
Immunohistochemical analysis of paraffin-embedded Human-brain, antibody was diluted at 1:100
Immunohistochemical analysis of paraffin-embedded Human-brain, antibody was diluted at 1:100