RDH13 抗体 (AA 101-200)
Quick Overview for RDH13 抗体 (AA 101-200) (ABIN1386807)
抗原
See all RDH13 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 101-200
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交叉反应
- 小鼠
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预测反应
- Human,Rat,Dog,Cow,Sheep,Horse,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human RDH13
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亚型
- IgG
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anti-Retinol Dehydrogenase 13 (All-Trans and 9-Cis) (RDH13) (AA 1-260) antibody
RDH13 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Retinol Dehydrogenase 13 (All-Trans and 9-Cis) (RDH13) (AA 166-194) antibodyRDH13 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB31711 unconjugated
anti-Retinol Dehydrogenase 13 (All-Trans and 9-Cis) (RDH13) (AA 173-202), (Middle Region) antibodyRDH13 适用: 人 WB, FACS, EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- RDH13 (Retinol Dehydrogenase 13 (All-Trans and 9-Cis) (RDH13))
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别名
- RDH13
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背景
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Synonyms: RDH13, RDH13_HUMAN, Retinol dehydrogenase 13 all trans and 9 cis, Retinol dehydrogenase 13 all trans/9 cis, Retinol dehydrogenase 13.
Background: RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.
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基因ID
- 112724
抗原
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