IFITM5 抗体 (PE-Cy5.5)
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- 抗原 See all IFITM5 抗体
- IFITM5 (Interferon Induced Transmembrane Protein 5 (IFITM5))
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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 IFITM5 antibody is conjugated to PE-Cy5.5
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应用范围
- Western Blotting (WB)
- 预测反应
- Human
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human IFITM5
- 亚型
- IgG
- Top Product
- Discover our top product IFITM5 Primary Antibody
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- 应用备注
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FCM(1:100-500)
Optimal working dilution should be determined by the investigator. - 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
- Sodium azide
- 注意事项
- This product contains sodium azide: 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
- IFITM5 (Interferon Induced Transmembrane Protein 5 (IFITM5))
- 别名
- IFITM5 (IFITM5 产品)
- 别名
- BRIL antibody, DSPA1 antibody, Hrmp1 antibody, OI5 antibody, fragilis4 antibody, 1110003J06Rik antibody, AW213665 antibody, Bril antibody, Hrtm1 antibody, interferon induced transmembrane protein 5 antibody, interferon-induced transmembrane protein 1 antibody, Ifitm5 antibody, IFITM5 antibody, LOC606890 antibody
- 背景
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Synonyms: Bone-restricted interferon-induced transmembrane protein-like protein, BRIL, Fragilis4, Hrmp1, ITM5, M5_HUMAN, Interferon-induced transmembrane protein 5.
Background: IFITM5 is a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195).
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