NIPA1 抗体 (AA 161-260) (Alexa Fluor 680)
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- 抗原 See all NIPA1 抗体
- NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))
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抗原表位
- AA 161-260
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This NIPA1 antibody is conjugated to Alexa Fluor 680
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应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human NIPA1
- 亚型
- IgG
- Top Product
- Discover our top product NIPA1 Primary Antibody
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- 应用备注
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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
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))
- 别名
- NIPA1 (NIPA1 产品)
- 别名
- FSP3 antibody, SPG6 antibody, 1110027G09Rik antibody, A830014A18Rik antibody, Spg6 antibody, non imprinted in Prader-Willi/Angelman syndrome 1 antibody, non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human) antibody, NIPA1 antibody, Nipa1 antibody
- 背景
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Synonyms: FSP 3, FSP3, Magnesium transporter NIPA1, MGC102724, MGC35570, NIPA 1, NIPA1, NIPA1_HUMAN, Non imprinted in Prader Willi/Angelman syndrome region protein 1, Non-imprinted in Prader-Willi/Angelman syndrome region protein 1, Spastic paraplegia 6 (autosomal dominant), Spastic paraplegia 6 protein, SPG 6, SPG6.
Background: This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]
- 基因ID
- 123606
- UniProt
- Q7RTP0
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