LETM1 抗体 (AA 101-200) (AbBy Fluor® 680)
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- 抗原 See all LETM1 抗体
- LETM1 (Leucine Zipper-EF-Hand Containing Transmembrane Protein 1 (LETM1))
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抗原表位
- AA 101-200
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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 LETM1 antibody is conjugated to AbBy Fluor® 680
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human LETM1
- 亚型
- IgG
- Top Product
- Discover our top product LETM1 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
- LETM1 (Leucine Zipper-EF-Hand Containing Transmembrane Protein 1 (LETM1))
- 别名
- LETM1 (LETM1 产品)
- 别名
- LETM1 antibody, wu:fc31h08 antibody, wu:fc58h01 antibody, zgc:109969 antibody, letm1 antibody, MGC145623 antibody, leucine zipper and EF-hand containing transmembrane protein 1 antibody, leucine zipper-EF-hand containing transmembrane protein 1 antibody, LETM1 and EF-hand domain-containing protein 1, mitochondrial antibody, LETM1 antibody, letm1 antibody, LOC100346816 antibody, Letm1 antibody
- 背景
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Synonyms: LETM 1, LETM1 and EF hand domain containing protein 1, mitochondrial, LETM1 and EF-hand domain-containing protein 1, Letm1, LETM1_HUMAN, Leucine zipper EF hand containing transmembrane protein 1, Leucine zipper-EF-hand-containing transmembrane protein 1, Mdm38 homolog, mitochondrial, ZNF300 bs-0628R
Background: This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq, Oct 2009].
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