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Human ferritin/FTL Protein, His tag

Ferritin light chain,Ferritin L subunit

价格 750.00 供应商现货 : 3-5个工作日
货号 S0A9062
规格
数量
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产品介绍 评论(0)

产品规格
  • 物种

    Human
  • 分子别名

    Ferritin light chain, Ferritin L subunit
  • Accession

    P02792
  • 表达序列

    Protein sequence (P02792, Met1-Asp175, with C-His tag) MSSQIRQNYSTDVEAAVNSLVNLYLQASYTYLSLGFYFDRDDVALEGVSHFFRELAEEKREGYERLLKMQNQRGGRALFQDIKKPAEDEWGKTPDAMKAAMALEKKLNQALLDLHALGSARTDPHLCDFLETHFLDEEVKLIKKMGDHLTNLHRLGGPEAGLGEYLFERLTLKHD

  • 表达宿主

    HEK293
  • 分子量

    Predicted MW: 21.7 kDa Observed MW: 22, 25-26 kDa

  • 纯度

    >95% by SDS-PAGE
  • 内毒素含量

    <0.1EU/μg
  • 标记

    Unconjugated
  • 标签

    with C-His tag
  • 性状

    Lyophilized Powder
  • 缓冲体系

    Lyophilized from a 0.2 μm filtered solution of 0.2M PBS, pH7.4.
  • 溶解方法

    Reconstitute no more than 1 mg/mL according to the size in deionized water after rapid centrifugation.
  • 储存条件

    12 months from date of receipt, -20 to -70 °C as supplied.
    6 months, -20 to -70 °C under sterile conditions after reconstitution.
    1 week, 2 to 8 °C under sterile conditions after reconstitution.
    Please avoid repeated freeze-thaw cycles.

背景介绍
  • Ferritin light chain is a protein that in humans is encoded by the FTL gene. Ferritin is the major protein responsible for storing intracellular iron in prokaryotes and eukaryotes. It is a heteropolymer consisting of 24 subunits, heavy and light ferritin chains. The function of the FTL is to act as both an iron reservoir and to remove excess iron from the body. The rates of iron uptake and release may be affected by changes to the components of the ferritin light chains and heavy chains. Although the ferritin light chain unlike the ferritin heavy chain has no ferroxidase activity, the light chain may be responsible for the electron transfer across the ferritin protein cage. Oxidative stress caused by iron radicals generated in the ETC and an increase in iron levels caused by defects in the FTL gene has been known to be a cause of the onset of neurodegenerative diseases and hyperferritinemia-cataract syndrome. Mutations of the FTL gene cause the rare adult-onset basal ganglia disease also known as neuroferritinopathy.

  • 电泳

    • 2μg(R: reducing conditions)

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