Recombinant 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.         

濃度：1mg/ ml

來源：Recombinant Human

純度：≥95% SDS-PAGE

表達系統(tǒng)：Escherichia coli

標簽：His tag   

蛋白長度：Full length protein

內毒素水平：<1.000 Eu/µg

純化方法：HPLC

應用：SDS-PAGE，Western blot，ELISA

Biological activity,immunology research

保存：-20℃

保質期：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.

多克隆抗體

產(chǎn)品名稱：Rabbit Anti-WTX antibody

Rabbit Anti-WTX 

別名：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.               

來源：Rabbit

克隆類型：Polyclonal

濃度：1mg/ml

亞型：IgG

反應：Rat (predicted: Human,Mouse,Sheep,Cow,Horse)

應用： 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

理論分子量：124kDa

免疫原：KLH conjugated synthetic peptide derived from human WTX

保存：-20℃
保質期：1年

 單克隆抗體

產(chǎn)品名稱：Anti-WTX antibody

Mouse Anti-WTX

別名：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.  

來源：Mouse

克隆類型：Monoclonal

濃度：1mg/ml

亞型：IgG

反應：Human

應用： 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  

反應:  Human

理論分子量：124kDa

免疫原：KLH conjugated synthetic peptide derived from human WTX

保存：-20℃
保質期：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.