FRMD8 抗体 (AA 65-170) (Cy7)
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- 抗原 See all FRMD8 抗体
- FRMD8 (FERM Domain Containing 8 (FRMD8))
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抗原表位
- AA 65-170
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适用
- 大鼠
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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 FRMD8 antibody is conjugated to Cy7
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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
- 大鼠
- 预测反应
- Human,Mouse,Dog,Cow,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FRMD8
- 亚型
- IgG
- Top Product
- Discover our top product FRMD8 Primary Antibody
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anti-FERM Domain Containing 8 (FRMD8) (AA 1-464) antibody
FRMD8 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-FERM Domain Containing 8 (FRMD8) (AA 217-452) antibodyFRMD8 适用: 人 WB 宿主: 兔 Polyclonal 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
- FRMD8 (FERM Domain Containing 8 (FRMD8))
- 别名
- FRMD8 (FRMD8 产品)
- 别名
- 1200004M23Rik antibody, 2310035N23Rik antibody, 4931429L16Rik antibody, AU018809 antibody, RGD1310323 antibody, FERM domain containing 8 antibody, FERM domain containing 8 L homeolog antibody, FRMD8 antibody, Frmd8 antibody, frmd8.L antibody
- 背景
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Synonyms: FERM domain containing protein 8, FKSG44, FRMD8_HUMAN.
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. FRMD8 (FERM domain-containing protein 8), also known as FKSG44, is a 464 amino acid protein containing one FERM domain. Existing as two alternatively spliced isoforms, the gene encoding FRMD8 maps to human chromosome 11q13.1. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
- 基因ID
- 83786
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