Receptor Accessory Protein 1 抗体 (AA 53-150) (Biotin)
Quick Overview for Receptor Accessory Protein 1 抗体 (AA 53-150) (Biotin) (ABIN1393117)
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 53-150
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交叉反应
- 小鼠
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预测反应
- Human,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,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 REEP1
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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
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
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储存方法
- Store at -20°C for 12 months.
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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
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Synonyms: C2orf23, Chromosome 2 open reading frame 23, FLJ13110, Receptor accessory protein 1, Receptor expression-enhancing protein 1, Reep1, REEP1_HUMAN, SPG31.
Background: Transport of G protein-coupled receptors (GPCRs) to the cell surface membrane is critical for receptor-ligand recognition. Mammalian GPCR odorant receptors (ORs), when heterologously expressed in cells, are poorly expressed on the cell surface. REEP1 (receptor expression-enhancing protein 1), is a 201 amino acid multi-pass mitochondrion membrane protein that belongs to the DP1 family. REEP1 interacts with odorant receptor proteins and may enhance the cell surface expression of odorant receptors. Mutations in the REEP1 gene are the third most common cause of hereditary spastic paraplegia (HSP) after spastin and atlastin gene mutations. Mutations in the REEP1 gene also cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. The REEP1 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, zebrafish, A.thaliana and rice, and maps to human chromosome 2p11.2.
抗原
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