Eyes Absent Homolog 1 (EYA1) (Middle Region) Peptide
EYA1
Reactivity: Human
Host: Synthetic
BP, WB, IHC
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- Target See all EYA1 products
- EYA1 (Eyes Absent Homolog 1 (EYA1))
- Protein Region
- Middle Region
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-EYA1 antibody (Catalog #: ARP32434_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- EYA1 (Eyes Absent Homolog 1 (EYA1))
- Synonyms
- EYA1 Peptide, bop Peptide, bor Peptide, XEya1 Peptide, wu:fc13c10 Peptide, zgc:100770 Peptide, BOP Peptide, BOR Peptide, BOS1 Peptide, EYA transcriptional coactivator and phosphatase 1 Peptide, EYA transcriptional coactivator and phosphatase 1 L homeolog Peptide, EYA1 Peptide, eya1 Peptide, Eya1 Peptide, eya1.L Peptide
- Background
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EYA1 is a member of the eyes absent (EYA) family of proteins. EYA1 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.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. Four transcript variants encoding three distinct isoforms have been identified for this gene.
Alias Symbols: BOP, BOR, MGC141875
Protein Interaction Partner: DACH1,GNAI2,GNAZ,SIX1,SIX2,SIX3,SIX1
Protein Size: 557 - Molecular Weight
- 61 kDa
- Gene ID
- 2138
- NCBI Accession
- NM_172060, NP_742057
- UniProt
- Q99502
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