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PLP1 抗体

The 兔 多克隆 anti-PLP1 antibody (ABIN2458050) specifically detects PLP1 in WB 和 ELISA. The antibody is reactive with 人, 大鼠, 小鼠 和 犬 samples.
产品编号 ABIN2458050
发货至: 中国
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北京 101111
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Beijing Economic Technological Development Area
Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for PLP1 抗体 (ABIN2458050)

抗原

See all PLP1 抗体
PLP1 (Proteolipid Protein 1 (PLP1))

适用

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人, 大鼠, 小鼠, 犬

宿主

  • 36
  • 10
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克隆类型

  • 40
  • 9
多克隆

标记

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This PLP1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by peptide affinity chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PLP1.
  • 应用备注

    PLP1 antibody can be used for detection of PLP1 by ELISA at 1:62500. PLP1 antibody can be used for detection of PLP1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store PLP1 antibody at -20 °C.
  • 抗原

    PLP1 (Proteolipid Protein 1 (PLP1))

    别名

    PLP1

    背景

    PLP1 is a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system. It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2.This gene encodes a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system. It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively spliced transcript variants encoding distinct isoforms or having different 5' UTRs, have been identified for this gene.

    分子量

    30 kDa

    基因ID

    5354

    NCBI登录号

    NP_000524

    UniProt

    P60201
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