Receptor Accessory Protein 1 抗体 (AA 61-110)
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Quick Overview for Receptor Accessory Protein 1 抗体 (AA 61-110) (ABIN7230988)
抗原
See all Receptor Accessory Protein 1 (REEP1) 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 61-110
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原理
- Rabbit Anti-REEP1 Polyclonal Antibody
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特异性
- The antibody detects endogenous levels of REEP1 protein
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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免疫原
- Synthesized peptide derived from part region of human REEP1 protein at AA range: 61-110
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亚型
- IgG
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anti-Receptor Accessory Protein 1 (REEP1) (AA 101-201) antibody
REEP1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Receptor Accessory Protein 1 (REEP1) (AA 110-159) antibodyREEP1 适用: 小鼠, 人, 大鼠, 犬, 马, 兔, Cow, 豚鼠, 猴, Bat, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-Receptor Accessory Protein 1 (REEP1) (C-Term) antibodyREEP1 适用: 小鼠, 人, 大鼠, 犬, 马, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Receptor Accessory Protein 1 (REEP1) (C-Term) antibodyREEP1 适用: 人, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Receptor Accessory Protein 1 (REEP1) (C-Term) antibodyREEP1 适用: 小鼠, 人, 大鼠, 犬, 马, 兔, Cow, 豚鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA
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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
- -20 °C
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储存方法
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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有效期
- 12 months
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- Receptor Accessory Protein 1 (REEP1)
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别名
- REEP1
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背景
- Receptor expression-enhancing protein 1, Spastic paraplegia 31 proteinREEP1 encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in REEP1 cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants.
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分子量
- 22kD
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基因ID
- 65055
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UniProt
- Q9H902
抗原
-
