Epigenetics & Nuclear Signaling Antibodies 4
Anti-EYA4 Antibody (CAB9638)
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- SKU:
- CAB9638
- Product Type:
- Antibody
- Applications:
- WB
- Applications:
- IHC
- Applications:
- FC
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Epigenetics and Nuclear Signaling
Description
| Antibody Name: | Anti-EYA4 Antibody |
| Antibody SKU: | CAB9638 |
| Antibody Size: | 100uL |
| Application: | WB IHC FC |
| Reactivity: | Human |
| Host Species: | Rabbit |
| Immunogen: | A synthetic Peptide of human EYA4 |
| Application: | WB IHC FC |
| Recommended Dilution: | WB 1:500 - 1:1000 IHC 1:20 - 1:50 FC 1:20 - 1:50 |
| Reactivity: | Human |
| Positive Samples: |
| Immunogen: | A synthetic Peptide of human EYA4 |
| Purification Method: | Affinity purification |
| Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| Isotype: | IgG |
| Sequence: | Email for sequence |
| Gene ID: | 2070 |
| Uniprot: | O95677 |
| Cellular Location: | Cytoplasm, Nucleus |
| Calculated MW: | 48kDa/63kDa/67kDa/69kDa |
| Observed MW: | Refer to figures |
| Synonyms: | EYA4, CMD1J, DFNA10 |
| Background: | This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant non-syndromic sensorineural 10 locus. The encoded protein is also a putative oncogene that mediates DNA repair, apoptosis, and innate immunity following DNA damage, cellular damage, and viral attack. Defects in this gene are also associated with dilated cardiomyopathy 1J. Alternative splicing results in multiple transcript variants encoding distinct isoforms. |
| UniProt Protein Function: | EYA4: Tyrosine phosphatase that specifically dephosphorylates 'Tyr-142' of histone H2AX (H2AXY142ph). 'Tyr-142' phosphorylation of histone H2AX plays a central role in DNA repair and acts as a mark that distinguishes between apoptotic and repair responses to genotoxic stress. Promotes efficient DNA repair by dephosphorylating H2AX, promoting the recruitment of DNA repair complexes containing MDC1. Its function as histone phosphatase probably explains its role in transcription regulation during organogenesis. May be involved in development of the eye. Defects in EYA4 are the cause of deafness autosomal dominant type 10 (DFNA10). DFNA10 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. Defects in EYA4 are the cause of cardiomyopathy dilated type 1J (CMD1J). Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Belongs to the HAD-like hydrolase superfamily. EYA family. 5 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:EC 3.1.3.48; Protein phosphatase, tyrosine (non-receptor) Chromosomal Location of Human Ortholog: 6q23 Molecular Function:protein binding Biological Process: anatomical structure morphogenesis; visual perception Disease: Cardiomyopathy, Dilated, 1j; Deafness, Autosomal Dominant 10 |
| NCBI Summary: | This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant non-syndromic sensorineural 10 locus. The encoded protein is also a putative oncogene that mediates DNA repair, apoptosis, and innate immunity following DNA damage, cellular damage, and viral attack. Defects in this gene are also associated with dilated cardiomyopathy 1J. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014] |
| UniProt Code: | O95677 |
| NCBI GenInfo Identifier: | 71153518 |
| NCBI Gene ID: | 2070 |
| NCBI Accession: | O95677.2 |
| UniProt Secondary Accession: | O95677,O95464, O95679, Q8IW39, Q9NTR7, B7Z7F7, |
| UniProt Related Accession: | O95677 |
| Molecular Weight: | 63,911 Da |
| NCBI Full Name: | Eyes absent homolog 4 |
| NCBI Synonym Full Names: | EYA transcriptional coactivator and phosphatase 4 |
| NCBI Official Symbol: | EYA4 |
| NCBI Official Synonym Symbols: | CMD1J; DFNA10 |
| NCBI Protein Information: | eyes absent homolog 4 |
| UniProt Protein Name: | Eyes absent homolog 4 |
| Protein Family: | Eyes absent |
| UniProt Gene Name: | EYA4 |
| UniProt Entry Name: | EYA4_HUMAN |
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