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LMAN1 抗体 (N-Term)

This 兔 多克隆 anti-LMAN1 antibody specifically detects LMAN1 in WB. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN635868
发货至: 中国
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Quick Overview for LMAN1 抗体 (N-Term) (ABIN635868)

抗原

See all LMAN1 抗体
LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))

适用

  • 71
  • 40
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  • 6
  • 2
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  • 2
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  • 1
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人, 小鼠, 大鼠

宿主

  • 69
  • 2

克隆类型

  • 36
  • 35
多克隆

标记

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  • 3
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  • 1
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  • 1
  • 1
  • 1
  • 1
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This LMAN1 antibody is un-conjugated

应用范围

  • 65
  • 39
  • 28
  • 25
  • 14
  • 14
  • 13
  • 5
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 15
    • 6
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    • 1
    • 1
    • 1
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    N-Term

    特异性

    LMAN1 antibody was raised against the N terminal of LMAN1

    纯化方法

    Affinity purified

    免疫原

    LMAN1 antibody was raised using the N terminal of LMAN1 corresponding to a region with amino acids DPAVALPHRRFEYKYSFKGPHLVQSDGTVPFWAHAGNAIPSSDQIRVAPS
  • 应用备注

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    说明

    LMAN1 Blocking Peptide, (ABIN937481), is also available for use as a blocking control in assays to test for specificity of this LMAN1 antibody

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of LMAN1 antibody in PBS

    浓度

    Lot specific

    缓冲液

    PBS

    注意事项

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    储存条件

    4 °C/-20 °C

    储存方法

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • 抗原

    LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))

    别名

    LMAN1

    背景

    LMAN1 is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in its gene are associated with a coagulation defect. Using positional cloning, its gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished.

    分子量

    54 kDa (MW of target protein)
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