EYA1 抗体
Quick Overview for EYA1 抗体 (ABIN2457953)
抗原
See all EYA1 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Antibody is purified by peptide affinity chromatography method.
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免疫原
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human EYA1.
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anti-Eyes Absent Homolog 1 (EYA1) (AA 100-170) antibody
EYA1 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Eyes Absent Homolog 1 (EYA1) (AA 100-250) antibodyEYA1 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Eyes Absent Homolog 1 (EYA1) (Middle Region) antibodyEYA1 适用: 人, 小鼠, 大鼠, 斑马鱼, Cow, 犬, 豚鼠, 兔, 马 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Eyes Absent Homolog 1 (EYA1) (AA 168-321) antibodyEYA1 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Eyes Absent Homolog 1 (EYA1) (Internal Region) antibodyVerified EYA1 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Eyes Absent Homolog 1 (EYA1) (C-Term) antibodyEYA1 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 兔, 马 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- EYA1 antibody can be used for detection of EYA1 by ELISA at 1:312500. EYA1 antibody can be used for detection of EYA1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
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浓度
- 1 mg/mL
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缓冲液
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
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注意事项
- As with any antibody avoid repeat freeze-thaw cycles.
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储存条件
- 4 °C/-20 °C
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储存方法
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store EYA1 antibody at -20 °C.
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- EYA1 (Eyes Absent Homolog 1 (EYA1))
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别名
- EYA1
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背景
- 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.
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分子量
- 61 kDa
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基因ID
- 2138
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NCBI登录号
- NP_742057
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UniProt
- Q99502
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途径
- Sensory Perception of Sound, Positive Regulation of Response to DNA Damage Stimulus
抗原
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