SETBP1 抗体 (AA 501-600) (AbBy Fluor® 350)
-
- 抗原 See all SETBP1 抗体
- SETBP1 (SET Binding Protein 1 (SETBP1))
-
抗原表位
- AA 501-600
-
适用
- 小鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This SETBP1 antibody is conjugated to AbBy Fluor® 350
-
应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SETBP1
- 亚型
- IgG
- Top Product
- Discover our top product SETBP1 Primary Antibody
-
-
- 应用备注
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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
- SETBP1 (SET Binding Protein 1 (SETBP1))
- 别名
- SETBP1 (SETBP1 产品)
- 别名
- SEB antibody, C130092E12 antibody, Seb antibody, mKIAA0437 antibody, NI36_04265 antibody, SET binding protein 1 antibody, SET-binding protein antibody, enterotoxin antibody, SETBP1 antibody, Setbp1 antibody, setbp1 antibody, LOC100080512 antibody, NI36_RS04255 antibody
- 背景
-
Synonyms: SEB, MRD29, SET-binding protein, SETBP1, KIAA0437
Background: SETBP1 (SET binding protein 1), also known as SEB, is a 1,542 amino acid nuclear protein that contains three AT hook DNA-binding domains, one SKI homology region and a C-terminal SET-binding domain, which is followed by three PPLPPPPP repeats. SETBP1 may be involved in SET-related tumorigenesis and leukemogenesis by regulating the transforming activity of SKI in the nucleus or suppressing SET function. As a widely expressed protein, SETBP1 is encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
- 基因ID
- 26040
- UniProt
- Q9Y6X0
-