4.1R (phospho Tyr660) Polyclonal Antibody

    • 货号:YP0468
    • 应用:WB;IHC;IF;ELISA
    • 种属:Human;Mouse
      • 靶点:
      • 4.1R
      • 基因名称:
      • EPB41
      • 蛋白名称:
      • Protein 4.1
      • Human Gene Id:
      • 2035
      • Human Swiss Prot No:
      • P11171
      • Mouse Swiss Prot No:
      • P48193
      • 免疫原:
      • The antiserum was produced against synthesized peptide derived from human EPB41 around the phosphorylation site of Tyr660/418. AA range:626-675
      • 特异性:
      • Phospho-4.1R (Y660) Polyclonal Antibody detects endogenous levels of 4.1R protein only when phosphorylated at Y660.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:5000.. IF 1:50-200
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • EPB41;E41P;Protein 4.1;P4.1;4.1R;Band 4.1;EPB4.1
      • 实测条带:
      • 60kD
      • 背景:
      • The protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Oct 2009],
      • 功能:
      • disease:Defects in EPB41 are a cause of hereditary pyropoikilocytosis (HPP) [MIM:266140]. HPP is an autosomal recessive hematologic disorder characterized by hemolytic anemia, microspherocytosis, poikilocytosis, and an unusual thermal sensitivity of red cells.,disease:Defects in EPB41 are the cause of elliptocytosis type 1 (EL1) [MIM:611804]. EL1 is a Rhesus-linked form of hereditary elliptocytosis, a genetically heterogeneous, autosomal dominant, hematologic disorder. It is characterized by variable hemolytic anemia and elliptical or oval red cell shape.,function:Protein 4.1 is a major structural element of the erythrocyte membrane skeleton. It plays a key role in regulating membrane physical properties of mechanical stability and deformability by stabilizing spectrin-actin interaction. Recruits DLG1 to membranes.,PTM:O-glycosylated; contains N-acetylglucosamine side chains in the C-ter
      • 细胞定位:
      • Cytoplasm, cytoskeleton . Cytoplasm, cell cortex . Nucleus .
      • 组织表达:
      • Brain,PCR rescued clones,Reticulocyte,Spleen,

      Accurate prediction of drug-induced heterogeneous response of red cell in vivo using a gravity-driven flow cytometry based on a microfluidic chip ANALYTICA CHIMICA ACTA Shuwen Liu WB Human
      货号:YP0468

      • 产品图片
      • Western Blot analysis of JK cells using Phospho-4.1R (Y660) Polyclonal Antibody
      • Western Blot analysis of Jurkat cells using Phospho-4.1R (Y660) Polyclonal Antibody
      • Western blot analysis of lysates from HepG2 cells treated with PMA 125ng/ml 30', using EPB41 (Phospho-Tyr660/418) Antibody. The lane on the right is blocked with the phospho peptide.
      • Immunohistochemical analysis of paraffin-embedded human meningioma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).