FSIP1 抗体 (AA 101-200) (Cy5)
Quick Overview for FSIP1 抗体 (AA 101-200) (Cy5) (ABIN1417686)
抗原
See all FSIP1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 101-200
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交叉反应
- 大鼠
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预测反应
- Human,Mouse,Dog,Cow,Sheep
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human FSIP1
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亚型
- IgG
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anti-Fibrous Sheath Interacting Protein 1 (FSIP1) (AA 101-400) antibody
FSIP1 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Fibrous Sheath Interacting Protein 1 (FSIP1) (AA 1-581) antibodyFSIP1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 3E12 unconjugated
anti-Fibrous Sheath Interacting Protein 1 (FSIP1) (AA 287-336) antibodyFSIP1 适用: 人, 大鼠, 小鼠, 兔, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Fibrous Sheath Interacting Protein 1 (FSIP1) (AA 1-260) antibodyFSIP1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Fibrous Sheath Interacting Protein 1 (FSIP1) (Middle Region) antibodyFSIP1 适用: 人, 大鼠, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Fibrous Sheath Interacting Protein 1 (FSIP1) (AA 55-287) antibodyFSIP1 适用: 人 WB, IHC, ICC, IP 宿主: 兔 Polyclonal unconjugated
anti-Fibrous Sheath Interacting Protein 1 (FSIP1) (AA 109-328) antibodyFSIP1 适用: 大鼠 WB, IHC, ICC, IP 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
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- FSIP1 (Fibrous Sheath Interacting Protein 1 (FSIP1))
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别名
- FSIP1
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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.
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基因ID
- 161835
抗原
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