SMCR7 抗体 (AA 201-300) (Alexa Fluor 488)
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- 抗原 See all SMCR7 抗体
- SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
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抗原表位
- AA 201-300
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适用
- 小鼠
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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 SMCR7 antibody is conjugated to Alexa Fluor 488
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应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Dog,Cow,Sheep,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SMCR7
- 亚型
- IgG
- Top Product
- Discover our top product SMCR7 Primary Antibody
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anti-Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7) (AA 1-454) antibody
SMCR7 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1F4 unconjugated
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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
- SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
- 别名
- SMCR7 (SMCR7 产品)
- 别名
- AI482195 antibody, Gm11 antibody, MID49 antibody, mid49 antibody, Smcr7 antibody, RGD1560728 antibody, SMCR7 antibody, im:7149098 antibody, smcr7 antibody, smcr7b antibody, zgc:152920 antibody, mitochondrial elongation factor 2 antibody, mitochondrial elongation factor 2 S homeolog antibody, Mief2 antibody, MIEF2 antibody, mief2.S antibody, mief2 antibody
- 背景
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Synonyms: MGC23130, MID49, MIEF2, Mitochondrial dynamic protein MID49, Mitochondrial dynamic protein of 49 kDa, Mitochondrial elongation factor 2, Smith Magenis syndrome chromosome region candidate 7, Smith-Magenis syndrome chromosomal region candidate gene 7 protein.
Background: This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]
- 基因ID
- 125170
- UniProt
- Q96C03
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