EYA1 抗体
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- 抗原 See all EYA1 抗体
- EYA1 (Eyes Absent Homolog 1 (EYA1))
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适用
- 人, 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This EYA1 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human EYA1
- 亚型
- IgG
- Top Product
- Discover our top product EYA1 Primary Antibody
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- 应用备注
- WB 1:200 - 1:2000
- 说明
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In the embryo, highly expressed in kidney with lower levels in brain, Weakly expressed in lung, In the adult, highly expressed in heart and skeletal muscle, Weakly expressed in brain and liver, No expression in eye or kidney
- 限制
- 仅限研究用
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- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20C. Avoid freeze / thaw cycles.
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- 抗原
- EYA1 (Eyes Absent Homolog 1 (EYA1))
- 别名
- EYA1 (EYA1 产品)
- 别名
- EYA1 antibody, bop antibody, bor antibody, XEya1 antibody, wu:fc13c10 antibody, zgc:100770 antibody, BOP antibody, BOR antibody, BOS1 antibody, EYA transcriptional coactivator and phosphatase 1 antibody, EYA transcriptional coactivator and phosphatase 1 L homeolog antibody, EYA1 antibody, eya1 antibody, Eya1 antibody, eya1.L antibody
- 背景
- 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.
- 分子量
- 64.593 kDa
- 基因ID
- 2138
- UniProt
- Q99502
- 途径
- Sensory Perception of Sound, Positive Regulation of Response to DNA Damage Stimulus
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