Fetal Hemoglobin Antibody, anti-human, Vio® B515, REAfinity™, 30 tests in 60 µL
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Fetal Hemoglobin Antibody, ant

i-human, Vio® B515, REAfinity™, 30 tests in 60 µL
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  • 询价
  • Miltenyi Biotec已认证
  • 德国
  • 130-129-262
  • 2025年12月09日
  • Intracellular flow cytometry
  • human cell line
  • human
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 免疫原

      Fetal Hemoglobin

    • 亚型

      recombinant human IgG1

    • 形态

      Reagents are supplied in buffer containing stabilizer and 0.05% sodium azide.

    • 保存条件

      避光,2-8℃

    • 克隆性

      REA533

    • 标记物

      Vio B515

    • 适应物种

      human

    • 保质期

      24个月

    • 供应商

      Miltenyi Biotec

    • 宿主

      human cell line

    • 应用范围

      Intracellular flow cytometry

    • 浓度

      1:50

    • 抗体英文名

      Fetal Hemoglobin Antibody, anti-human, REAfinity™

    • 抗体名

      Fetal Hemoglobin Antibody, anti-human, REAfinity™

    • 规格

      30 tests in 60 µL

    Identification and enumeration of fetal hemoglobin+ cells by flow cytometryClone REA533 recognizes the human fetal hemoglobin (HbF) antigen, a form of hemoglobin present during fetal development. The hemoglobin molecule is a tetramer composed of two subunits of α-like globin peptide chains and two subunits of the β-like globin peptides, along with heme moieties necessary for this molecule´s oxygen-carrying capacity. When production of the first enucleated definitive erythrocytes commences from stem and progenitor cells in the fetal liver, the predominant β-like globin molecule produced is γ-globin. The γ-globin chains combine with adult α-globin chains into a stable tetramer forming HbF. Shortly after the time of birth there is a switch from predominant expression of HbF to adult hemoglobin (HbA), which is mediated by a transcriptional switch in definitive erythroid progenitors from γ- to β-globin. The synthesis of HbF is normally reduced to very low levels of less than 0.6% of the total hemoglobin in adults. HbF levels may be increased in adults in a number of inherited and acquired disorders. The clinical significance of these conditions with raised HbF relates to their interaction in disorders such as sickle cell disease and β-thalassemia in which raised levels of HbF can lead to considerable amelioration of disease severity. | Additional information: Clone REA533 displays negligible binding to Fc receptors.

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    图标文献和实验
    该产品被引用文献
    Akinsheye, I. et al. (2011) Fetal hemoglobin in sickle cell anemia. Blood 118 (1): 19–27. | Rochette, J. et al. (1994) Fetal hemoglobin levels in adults. Blood 8 (4): 213–224. | Sankaran, V. G. et al. (2008) Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A. Science 322 (5909): 1839–1842.
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    Fetal Hemoglobin Antibody, anti-human, Vio® B515, REAfinity™, 30 tests in 60 µL
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