FSIP1 抗体 (AA 101-200) (AbBy Fluor® 680)
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- 抗原 See all FSIP1 抗体
- FSIP1 (Fibrous Sheath Interacting Protein 1 (FSIP1))
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抗原表位
- AA 101-200
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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 FSIP1 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
- 大鼠
- 预测反应
- Human,Mouse,Dog,Cow,Sheep
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FSIP1
- 亚型
- IgG
- Top Product
- Discover our top product FSIP1 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
- FSIP1 (Fibrous Sheath Interacting Protein 1 (FSIP1))
- 别名
- FSIP1 (FSIP1 产品)
- 别名
- zgc:113106 antibody, 1700012M13Rik antibody, 4933432K11Rik antibody, fibrous sheath interacting protein 1 antibody, fibrous sheath-interacting protein 1 antibody, FSIP1 antibody, Fsip1 antibody, fsip1 antibody
- 背景
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Synonyms: Fibrous sheath interacting protein 1, FLJ35989, HSD10, FSIP1_HUMAN.
Background: FSIP1 is a 581 amino acid protein that is expressed in airway epithelium. A member of the FSIP1 family, FSIP1 is encoded by a gene that maps to human chromosome 15q14 and mouse chromosome 2 E5. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
- 基因ID
- 161835
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