ATL1 抗体 (AA 24-552)
Quick Overview for ATL1 抗体 (AA 24-552) (ABIN7600846)
抗原
See all ATL1 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 24-552
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原理
- Anti-ATL1 Antibody Picoband®
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产品特性
- Anti-ATL1 Antibody Picoband® (ABIN7600846). Tested in WB, ICC/IF, Flow Cytometry, ELISA applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human ATL1 recombinant protein (Position: E24-Q552). Human ATL1 shares 97.5% and 98.3% amino acid (aa) sequence identity with mouse and rat ATL1, respectively.
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anti-Atlastin GTPase 1 (ATL1) (AA 1-100) antibody
ATL1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1B9 unconjugated
anti-Atlastin GTPase 1 (ATL1) (N-Term) antibodyATL1 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Atlastin GTPase 1 (ATL1) (AA 1-100) antibodyATL1 适用: 人 ELISA 宿主: 小鼠 Monoclonal 1F6B12 unconjugated
anti-Atlastin GTPase 1 (ATL1) (AA 1-280) antibodyATL1 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Atlastin GTPase 1 (ATL1) (AA 220-350) antibodyATL1 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Atlastin GTPase 1 (ATL1) antibodyATL1 适用: 人, 小鼠, 大鼠 WB, IF, IC 宿主: 兔 Polyclonal unconjugated
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应用备注
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Western blot, 0.25-0.5 μg/mL, Human
Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/mL, -
1. Abel, A., Fonknechten, N., Hofer, A., Durr, A., Cruaud, C., Voit, T., Weissenbach, J., Brice, A., Klimpe, S., Auburger, G., Hazan, J. Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A. Neurogenetics 5: 239-243, 2004. 2. Beetz, C., Nygren, A. O. H., Deufel, T., Reid, E. An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 mutation. (Letter) Neurogenetics 8: 317-318, 2007. 3. D'Amico, A., Tessa, A., Sabino, A., Bertini, E., Santorelli, F. M., Servidei, S. Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene. Neurology 62: 2138-2139, 2004. -
限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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浓度
- 500 μg/mL
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缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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储存条件
- 4 °C,-20 °C
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储存方法
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
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- ATL1 (Atlastin GTPase 1 (ATL1))
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别名
- ATL1
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背景
- Atlastin, or Atlastin-1, is a protein that in humans is encoded by the ATL1 gene. The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene.
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分子量
- 64 kDa
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基因ID
- 51062
抗原
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