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    2. 最近搜索:細胞培養 微生物學 分子生物 生物化學
      首頁>>免疫學>>一抗>>負調控因子白細胞介素2抗體
      負調控因子白細胞介素2抗體
      • 產品貨號:
        BN41894R
      • 中文名稱:
        負調控因子白細胞介素2抗體
      • 英文名稱:
        Rabbit anti-ZEB1/NIL2A Polyclonal antibody
      • 品牌:
        Biorigin
      • 貨號

        產品規格

        售價

        備注

      • BN41894R-50ul

        50ul

        ¥1486.00

        交叉反應:Human,Mouse,Rat(predicted:Chicken,Dog,Pig,Cow,Rabbit) 推薦應用:WB,IHC-P,Flow-Cyt,ELISA

      • BN41894R-100ul

        100ul

        ¥2360.00

        交叉反應:Human,Mouse,Rat(predicted:Chicken,Dog,Pig,Cow,Rabbit) 推薦應用:WB,IHC-P,Flow-Cyt,ELISA

      • BN41894R-200ul

        200ul

        ¥3490.00

        交叉反應:Human,Mouse,Rat(predicted:Chicken,Dog,Pig,Cow,Rabbit) 推薦應用:WB,IHC-P,Flow-Cyt,ELISA

      產品描述

      英文名稱ZEB1/NIL2A
      中文名稱負調控因子白細胞介素2抗體
      別    名AREB 6; AREB6; BZP; Delta crystallin enhancer binding factor 1; DELTA EF1; FECD6; MGC133261; Negative regulator of IL 2; Negative regulator of IL2; NIL 2 A; NIL 2 A zinc finger protein; NIL 2A; NIL-2-A zinc finger protein; NIL2A; Posterior polymorphous corneal dystrophy 3; PPCD3; Represses interleukin 2 expression; TCF 8; TCF-8; TCF8; Transcription factor 8 (represses interleukin 2 expression); Transcription factor 8; ZEB 1; ZEB;ZEB1_HUMAN; ZFHEP; ZFHX 1A; ZFHX1A; Zinc finger E box binding homeobox 1; Zinc finger E-box-binding homeobox 1; Zinc finger homeodomain enhancer binding protein.  




      研究領域腫瘤  染色質和核信號  信號轉導  表觀遺傳學  
      抗體來源Rabbit
      克隆類型Polyclonal
      交叉反應Human, Mouse, Rat,  (predicted: Chicken, Dog, Pig, Cow, Rabbit, )
      產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 Flow-Cyt=1μg/Test (石蠟切片需做抗原修復)
      not yet tested in other applications.
      optimal dilutions/concentrations should be determined by the end user.
      分 子 量124kDa
      細胞定位細胞核 
      性    狀Liquid
      濃    度1mg/ml
      免 疫 原KLH conjugated synthetic peptide derived from human ZEB1:211-320/1124 
      亞    型IgG
      純化方法affinity purified by Protein A
      儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
      保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
      PubMedPubMed
      產品介紹This gene encodes a zinc finger transcription factor. The encoded protein likely plays a role in transcriptional repression of interleukin 2. Mutations in this gene have been associated with posterior polymorphous corneal dystrophy-3 and late-onset Fuchs endothelial corneal dystrophy. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2010]

      Function:
      Acts as a transcriptional repressor. Inhibits interleukin-2 (IL-2) gene expression. Enhances or represses the promoter activity of the ATP1A1 gene depending on the quantity of cDNA and on the cell type. Represses E-cadherin promoter and induces an epithelial-mesenchymal transition (EMT) by recruiting SMARCA4/BRG1. Represses BCL6 transcription in the presence of the corepressor CTBP1. Positively regulates neuronal differentiation. Represses RCOR1 transcription activation during neurogenesis. Represses transcription by binding to the E box (5'-CANNTG-3'). Promotes tumorigenicity by repressing stemness-inhibiting microRNAs.

      Subunit:
      Interacts (via N-terminus) with SMARCA4/BRG1.

      Subcellular Location:
      Nucleus.

      Tissue Specificity:
      Colocalizes with SMARCA4/BRG1 in E-cadherin-negative cells from established lines, and stroma of normal colon as well as in de-differentiated epithelial cells at the invasion front of colorectal carcinomas (at protein level). Expressed in heart and skeletal muscle, but not in liver, spleen, or pancreas.

      DISEASE:
      Corneal dystrophy, posterior polymorphous, 3 (PPCD3) [MIM:609141]: A subtype of posterior corneal dystrophy, a disease characterized by alterations of Descemet membrane presenting as vesicles, opacities or band-like lesions on slit-lamp examination and specular microscopy. Affected patient typically are asymptomatic. Note=The disease is caused by mutations affecting the gene represented in this entry.
      Corneal dystrophy, Fuchs endothelial, 6 (FECD6) [MIM:613270]: A corneal disease caused by loss of endothelium of the central cornea. It is characterized by focal wart-like guttata that arise from Descemet membrane and develop in the central cornea, epithelial blisters, reduced vision and pain. Descemet membrane is thickened by abnormal collagenous deposition. Note=The disease is caused by mutations affecting the gene represented in this entry.

      Similarity:
      Belongs to the delta-EF1/ZFH-1 C2H2-type zinc-finger family.
      Contains 7 C2H2-type zinc fingers.
      Contains 1 homeobox DNA-binding domain.

      SWISS:
      P37275

      Gene ID:
      6935

      Database links:

      Entrez Gene: 396029 Chicken

      Entrez Gene: 535183 Cow

      Entrez Gene: 6935 Human

      Entrez Gene: 21417 Mouse

      Entrez Gene: 25705 Rat

      Omim: 189909 Human

      SwissProt: P36197 Chicken

      SwissProt: P37275 Human



      Important Note:
      This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.


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