技术文章
TECHNICAL ARTICLESRecombinant human WTX
FAM123B; AMER1; FAM 123B; AMER1_HUMAN; Family with sequence similarity 123B; FLJ39827; OSCS; Protein FAM123B; RP11 403E24.2; Wilms tumor gene on the X chromosome protein; Wilms tumor on the X; WTX.
浓度:1mg/ ml
来源:Recombinant Human
纯度:≥95% SDS-PAGE
表达系统:Escherichia coli
标签:His tag
蛋白长度:Full length protein
内毒素水平:<1.000 Eu/µg
纯化方法:HPLC
应用:SDS-PAGE,Western blot,ELISA
Biological activity,immunology research
保存:-20℃
保质期:1年
The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).FAM123B enhances trancription activation by WT1. It also promotes CTNNB1 ubiquitination and degradation and antagonizes Wnt and CTNNB1 signaling. FAM123B is involved in kidney development.
多克隆抗体
产品名称:Rabbit Anti-WTX antibody
Rabbit Anti-WTX
别名:FAM123B; AMER1; FAM 123B; AMER1_HUMAN; Family with sequence similarity 123B; FLJ39827; OSCS; Protein FAM123B; RP11 403E24.2; Wilms tumor gene on the X chromosome protein; Wilms tumor on the X; WTX.
来源:Rabbit
克隆类型:Polyclonal
浓度:1mg/ml
亚型:IgG
反应:Rat (predicted: Human,Mouse,Sheep,Cow,Horse)
应用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500
理论分子量:124kDa
免疫原:KLH conjugated synthetic peptide derived from human WTX
保存:-20℃
保质期:1年
单克隆抗体
产品名称:Anti-WTX antibody
Mouse Anti-WTX
别名:FAM123B; AMER1; FAM 123B; AMER1_HUMAN; Family with sequence similarity 123B; FLJ39827; OSCS; Protein FAM123B; RP11 403E24.2; Wilms tumor gene on the X chromosome protein; Wilms tumor on the X; WTX.
来源:Mouse
克隆类型:Monoclonal
浓度:1mg/ml
亚型:IgG
反应:Human
应用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500
反应: Human
理论分子量:124kDa
免疫原:KLH conjugated synthetic peptide derived from human WTX
保存:-20℃
保质期:1年
The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).FAM123B enhances trancription activation by WT1. It also promotes CTNNB1 ubiquitination and degradation and antagonizes Wnt and CTNNB1 signaling. FAM123B is involved in kidney development.