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              當(dāng)前位置:首頁資料下載Wnt1抗原,信號(hào)通路Wnt1抗原

              Wnt1抗原,信號(hào)通路Wnt1抗原

              發(fā)布時(shí)間:2024/11/10點(diǎn)擊次數(shù):29

              Recombinant human Wnt1   

              wingless-type MMTV integration site family, member 1; INT 1; INT1; Murine mammary tumor virus integration site 1 ; Oncogene INT1; Proto oncogene protein Wnt 1; Wnt 1; Wnt1 proto oncogene protein precursor; WNT1_HUMAN.    

              濃度:1mg/ ml

              來源:Recombinant Human

              純度:95% SDS-PAGE

              表達(dá)系統(tǒng):Escherichia coli

              標(biāo)簽:His tag   

              蛋白長度:Full length protein

              內(nèi)毒素水平:<1.000 Eu/µg

              純化方法:HPLC

              應(yīng)用:SDS-PAGEWestern blotELISA

              Biological activity,immunology research

              保存:-20

              保質(zhì)期:1

              TThe WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.



              產(chǎn)品名稱:Rabbit Anti-Wnt1 antibody

              Rabbit Anti-Wnt1 

              別名:wingless-type MMTV integration site family, member 1; INT 1; INT1; Murine mammary tumor virus integration site 1 ; Oncogene INT1; Proto oncogene protein Wnt 1; Wnt 1; Wnt1 proto oncogene protein precursor; WNT1_HUMAN.               

              來源:Rabbit

              克隆類型:Polyclonal

              濃度:1mg/ml

              亞型:IgG

              反應(yīng):Human,Mouse,Rat (predicted: Cow,Chicken,Horse)

              應(yīng)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:39kDa

              免疫原:KLH conjugated synthetic peptide derived from human Wnt1

              保存:-20
              保質(zhì)期:1

               

               

              產(chǎn)品名稱:Anti-Wnt1 antibody

              Mouse Anti-Wnt1

              別名:wingless-type MMTV integration site family, member 1; INT 1; INT1; Murine mammary tumor virus integration site 1 ; Oncogene INT1; Proto oncogene protein Wnt 1; Wnt 1; Wnt1 proto oncogene protein precursor; WNT1_HUMAN.                   

              來源:Mouse

              克隆類型:Monoclonal

              濃度:1mg/ml

              亞型:IgG

              反應(yīng):Human

              應(yīng)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(yīng):  Human

              理論分子量:39kDa

              免疫原:KLH conjugated synthetic peptide derived from human Wnt1

              保存:-20
              保質(zhì)期:1

              The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.


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