PRRT2 抗体 (AA 180-230)
Quick Overview for PRRT2 抗体 (AA 180-230) (ABIN6991846)
抗原
See all PRRT2 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 180-230
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特异性
- Multiple isoforms of PRRT2 are known to exist.
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纯化方法
- PRRT2 Antibody is affinity chromatography purified via peptide column.
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免疫原
- PRRT2 antibody was raised against a 18 amino acid peptide near the center of human PRRT2 . The immunogen is located within amino acids 180 - 230 of PRRT2.
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亚型
- IgG
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anti-Proline-Rich Transmembrane Protein 2 (PRRT2) (AA 207-233) antibody
PRRT2 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB37969 unconjugated
anti-Proline-Rich Transmembrane Protein 2 (PRRT2) (AA 1-340) antibodyPRRT2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Proline-Rich Transmembrane Protein 2 (PRRT2) (AA 20-130) antibodyPRRT2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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PRRT2 Antibody can be used for detection of PRRT2 by Western blot at 1 μ,g/mL.
Antibody validated: Western Blot in mouse samples, Immunohistochemistry in rat samples and Immunofluorescence in rat samples. All other applications and species not yet tested. -
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
- PRRT2 Antibody is supplied in PBS containing 0.02 % sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C,4 °C
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储存方法
- PRRT2 antibody can be stored at 4°C for three months and -20°C, stable for up to one year.
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- PRRT2 (Proline-Rich Transmembrane Protein 2 (PRRT2))
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别名
- PRRT2
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背景
- PRRT2 Antibody: The proline-rich transmembrane protein 2 (PRRT2) contains a proline-rich domain in its N-terminal half and is predominantly expressed in brain and spinal cord in embryonic and postnatal stages. While little is known of the function of this protein, mutations in PRRT2 have been shown to be the causative gene of paroxysmal kinesigenic dyskinesia, which is characterized by recurrent, brief attacks of abnormal involuntary movements induced by sudden voluntary movements. Recent studies have shown that PRRT2 may also be involved in some forms of benign familial infantile epilepsy (BFIE), an autosomal dominant epilepsy syndrome.
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分子量
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Predicted: 43 kDa
Observed: 44 kDa -
基因ID
- 112476
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NCBI登录号
- NP_001243371
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UniProt
- Q7Z6L0
抗原
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