Eyes Absent Homolog 1 (EYA1) (Middle Region) Peptide
EYA1
适用: 人
宿主: 合成
BP, WB, IHC
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- 抗原 See all EYA1 products
- EYA1 (Eyes Absent Homolog 1 (EYA1))
- 蛋白结构域
- Middle Region
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- 产品特性
- 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.
- 纯化方法
- Purified
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- EYA1 (Eyes Absent Homolog 1 (EYA1))
- 别名
- 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
- 背景
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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 - 分子量
- 61 kDa
- 基因ID
- 2138
- NCBI登录号
- NM_172060, NP_742057
- UniProt
- Q99502
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