FRMD5 抗体 (AA 211-312) (AbBy Fluor® 647)
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- 抗原 See all FRMD5 products
- FRMD5 (FERM Domain Containing 5 (FRMD5))
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抗原表位
- AA 211-312
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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 FRMD5 antibody is conjugated to AbBy Fluor® 647
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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,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FRMD5
- 亚型
- IgG
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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
- FRMD5 (FERM Domain Containing 5 (FRMD5))
- 别名
- FRMD5 (FRMD5 产品)
- 别名
- 1500032A09Rik antibody, 5830442F04 antibody, A930004K21Rik antibody, R75430 antibody, RGD1561554 antibody, FRMD5 antibody, FERM domain containing 5 antibody, FRMD5 antibody, Frmd5 antibody, frmd5 antibody
- 背景
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Synonyms: FERM domain containing 5, FERM domain-containing protein 5, FLJ41022, FRMD5, FRMD5_HUMAN, MGC14161.
Background: FERM domains are roughly 150 amino acids in length and are found in a number of cytoskeletal-associated proteins such as Ezrin, Radixin, Moesin and 4.1 (erythrocyte membrane protein band 4.1), where they provide a link between cytoskeletal signals and membrane dynamics. FRMD5 (FERM domain-containing protein 5) is a 570 amino acid single-pass membrane protein that contains one FERM domain and exists as two alternatively spliced isoforms. The gene encoding FRMD5 maps to human chromosome 15, which houses over 700 genes and comprises nearly 3 % of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
- 基因ID
- 84978
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