Tetraspanin 9 抗体 (AA 180-203) (Cy5)
Quick Overview for Tetraspanin 9 抗体 (AA 180-203) (Cy5) (ABIN1420638)
抗原
See all Tetraspanin 9 (TSPAN9) 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 180-203
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交叉反应
- 人, 小鼠, 大鼠
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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 TSPAN9
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亚型
- IgG
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anti-Tetraspanin 9 (TSPAN9) (AA 180-203) antibody
TSPAN9 适用: 人, 小鼠, 大鼠 WB, FACS, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Tetraspanin 9 (TSPAN9) (AA 107-203) antibodyTSPAN9 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Tetraspanin 9 (TSPAN9) (Internal Region) antibodyTSPAN9 适用: 人, 小鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Tetraspanin 9 (TSPAN9) (Center) antibodyTSPAN9 适用: 人, 小鼠, 大鼠 WB, EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
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FCM 1:20-100
IF(IHC-P) 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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- Tetraspanin 9 (TSPAN9)
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别名
- TSPAN9
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背景
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Synonyms: NET5, NET-5, PP1057, Tetraspanin-9, Tspan-9, Tetraspan NET-5, TSPAN9
Background: The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
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基因ID
- 10867
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UniProt
- O75954
抗原
-
