Tetraspanin 9 抗体 (AA 180-203) (Cy5)
-
- 抗原 See all Tetraspanin 9 (TSPAN9) 抗体
- Tetraspanin 9 (TSPAN9)
-
抗原表位
- AA 180-203
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This Tetraspanin 9 antibody is conjugated to Cy5
-
应用范围
- Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human TSPAN9
- 亚型
- IgG
- Top Product
- Discover our top product TSPAN9 Primary Antibody
-
-
- 应用备注
-
FCM 1:20-100
IF(IHC-P) 1:50-200 - 限制
- 仅限研究用
-
- 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
-
- 抗原
- Tetraspanin 9 (TSPAN9)
- 别名
- TSPAN9 (TSPAN9 产品)
- 别名
- NET5 antibody, TNE5 antibody, TSPAN9 antibody, Tspan-9 antibody, NET-5 antibody, PP1057 antibody, 6720474K14Rik antibody, 9430079M16Rik antibody, AU018597 antibody, RGD1304740 antibody, MGC80926 antibody, si:dkey-261a10.1 antibody, tspan9 antibody, tetraspanin 9 antibody, tetraspanin 9 S homeolog antibody, tetraspanin 9a antibody, Tetraspanin-9 antibody, TSPAN9 antibody, Tspan9 antibody, tspan9.S antibody, tspan9a antibody, tspan9 antibody, tsn9 antibody
- 背景
-
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.
- 基因ID
- 10867
- UniProt
- O75954
-