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BPGM 抗体 (Biotin)

BPGM 适用: 人, 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1403197
发货至: 中国
  • 抗原 See all BPGM 抗体
    BPGM (2,3-bisphosphoglycerate Mutase (BPGM))
    适用
    • 53
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    人, 小鼠, 大鼠
    宿主
    • 53
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    克隆类型
    • 53
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    多克隆
    标记
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    This BPGM antibody is conjugated to Biotin
    应用范围
    • 47
    • 18
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    • 13
    • 8
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    • 4
    • 3
    • 1
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    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human BPGM
    亚型
    IgG
    Top Product
    Discover our top product BPGM Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C for 12 months.
    有效期
    12 months
  • 抗原
    BPGM (2,3-bisphosphoglycerate Mutase (BPGM))
    别名
    BPGM (BPGM 产品)
    别名
    DPGM antibody, AI323730 antibody, AL022789 antibody, C86192 antibody, Ab2-098 antibody, zgc:92230 antibody, Bisphosphoglycerate mutase antibody, bisphosphoglycerate mutase antibody, 2,3-bisphosphoglycerate mutase antibody, bisphosphoglycerate mutase S homeolog antibody, pmge antibody, BPGM antibody, Bpgm antibody, bpgm antibody, bpgm.S antibody
    背景

    Synonyms: 2,3-bisphosphoglycerate mutase, 2,3-bisphosphoglycerate synthase, 3-bisphosphoglycerate mutase, 3-bisphosphoglycerate synthase, 3-diphosphoglycerate mutase, Ab2 098, AI323730, AL022789, Bisphosphoglycerate mutase, BPG dependent PGAM, BPG-dependent PGAM , Bpgm, BPGM, C86192, DPGM, Erythrocyte 2,3 bisphosphoglycerate mutase, PMGE_HUMAN, 2,3-bisphosphoglycerate mutase, erythrocyte, erythrocyte, 2 antibody.

    Background: BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease:Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD) . A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.

    基因ID
    669
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