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LAT2 抗体 (C-Term)

LAT2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2856388
发货至: 中国
  • 抗原 See all LAT2 抗体
    LAT2 (Linker For Activation of T Cells Family, Member 2 (LAT2))
    抗原表位
    • 8
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    C-Term
    适用
    • 54
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    宿主
    • 47
    • 15
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    克隆类型
    • 48
    • 15
    多克隆
    标记
    • 40
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    This LAT2 antibody is un-conjugated
    应用范围
    • 52
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    Western Blotting (WB)
    交叉反应
    产品特性
    Rabbit polyclonal antibody to NTAL (linker for activation of T cells family, member 2)
    NTAL antibody [C2C3], C-term
    纯化方法
    Purified by antigen-affinity chromatography.
    免疫原
    Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human NTAL. The exact sequence is proprietary.
    亚型
    IgG
    Top Product
    Discover our top product LAT2 Primary Antibody
  • 应用备注
    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
    说明

    Positive Control: Raji

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.62 mg/mL
    缓冲液
    0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal
    储存液
    Thimerosal (Merthiolate)
    注意事项
    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原
    LAT2 (Linker For Activation of T Cells Family, Member 2 (LAT2))
    别名
    linker for activation of T cells family member 2 (LAT2 产品)
    别名
    LAB antibody, NTAL antibody, WBSCR15 antibody, WBSCR5 antibody, WSCR5 antibody, LAT2 antibody, MGC139435 antibody, Ntal antibody, Wbscr5 antibody, AW125574 antibody, Wbscr15 antibody, linker for activation of T-cells family member 2 antibody, linker for activation of T cells family, member 2 antibody, LAT2 antibody, Lat2 antibody
    背景
    This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.

    Cellular Localization: Cell membrane, Single-pass type III membrane protein
    分子量
    27 kDa
    基因ID
    7462
    UniProt
    Q9GZY6
    途径
    Fc-epsilon Receptor Signaling Pathway, BCR Signaling
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