EYA1/EYA4 rabbit pAb
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],
Product Specifications
Background
UniProt
Q99502/O95677
Swiss Prot
Q99502/O95677
Reactivity
Human; Mouse
Immunogen
Synthetic peptide from human protein at AA range: 271-320
Clonality
Polyclonal
Source
Rabbit
Applications
IHC; IF; ELISA
Concentration
1 mg/ml
Dilution
IHC-p 1:50-200, ELISA 1:10000-20000
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Cytoplasm . Nucleus . Localizes at sites of DNA damage at double-strand breaks (DSBs) . .
Gene ID (Human)
2138/2140
Available Sizes
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