CRX 抗体 (AA 265-299)
Quick Overview for CRX 抗体 (AA 265-299) (ABIN5647525)
抗原
See all CRX 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 265-299
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纯化方法
- Antigen affinity purified
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免疫原
- Amino acids 265-299 (DSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL) from the human protein were used as the immunogen for the CRX antibody.
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亚型
- IgG
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anti-Cone-Rod Homeobox (CRX) (AA 1-95) antibody
CRX 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4G11 unconjugated
anti-Cone-Rod Homeobox (CRX) (AA 1-300) antibodyCRX 适用: 人 WB, ELISA, RNAi 宿主: 小鼠 Monoclonal F6-C2 unconjugated
anti-Cone-Rod Homeobox (CRX) (AA 120-285) antibodyCRX 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Cone-Rod Homeobox (CRX) (AA 1-299) antibodyCRX 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 4A12 unconjugated
anti-Cone-Rod Homeobox (CRX) (AA 51-150) antibodyCRX 适用: 大鼠, 小鼠 ELISA, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Cone-Rod Homeobox (CRX) (AA 120-285) antibodyCRX 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Cone-Rod Homeobox (CRX) (Internal Region) antibodyVerified CRX 适用: 人, 大鼠 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Cone-Rod Homeobox (CRX) (AA 1-95) antibodyCRX 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Cone-Rod Homeobox (CRX) (AA 294-297), (C-Term) antibodyCRX 适用: 人 WB 宿主: 兔 Polyclonal RB49208 unconjugated
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应用备注
- Optimal dilution of the CRX antibody should be determined by the researcher.\. WB: 0.5-1 μg/mL
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限制
- 仅限研究用
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- -20 °C
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储存方法
- After reconstitution, the CRX antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
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- CRX (Cone-Rod Homeobox (CRX))
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别名
- CRX (Cone-rod homeobox)
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背景
- Cone-rod homeobox protein is a protein that in humans is encoded by the CRX gene. The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.
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UniProt
- O43186
抗原
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