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FECH 抗体 (N-Term)

This anti-FECH antibody is a 兔 多克隆 antibody detecting FECH in WB 和 IHC. Suitable for 人 和 大鼠.
产品编号 ABIN2777033
发货至: 中国

Quick Overview for FECH 抗体 (N-Term) (ABIN2777033)

抗原

See all FECH 抗体
FECH (Ferrochelatase (FECH))

适用

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人, 大鼠

宿主

  • 35
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克隆类型

  • 37
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多克隆

标记

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This FECH antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

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    N-Term

    序列

    QHAQGAKPQV QPQKRYESNI RKPKTGILML NMGGPETLGD VHDFLLRLFL

    预测反应

    Human: 100%, Rat: 86%

    产品特性

    This is a rabbit polyclonal antibody against FECH. It was validated on Western Blot and immunohistochemistry.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the N terminal region of human FECH
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 429 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    FECH (Ferrochelatase (FECH))

    别名

    FECH

    背景

    Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria.Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene.Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene.
    Alias Symbols: EPP, FCE
    Protein Interaction Partner: PPP2R1A, UBC, NEDD8, MDM2, FBXO6, gag-pol, COPS5, COPS6, CUL3, ELAVL1, MINOS1, MME, USP42, USP20, ABCB7, FECH,
    Protein Size: 429

    分子量

    47 kDa

    基因ID

    2235

    NCBI登录号

    NM_001012515, NP_001012533

    UniProt

    Q8NAN0

    途径

    Transition Metal Ion Homeostasis
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