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FECH 抗体

FECH 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1385988
发货至: 中国
  • 抗原 See all FECH 抗体
    FECH (Ferrochelatase (FECH))
    适用
    • 31
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    人, 小鼠, 大鼠
    宿主
    • 27
    • 4
    克隆类型
    • 29
    • 2
    多克隆
    标记
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    This FECH antibody is un-conjugated
    应用范围
    • 30
    • 12
    • 9
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human EPB41
    亚型
    IgG
    Top Product
    Discover our top product FECH Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: 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
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    有效期
    12 months
  • 抗原
    FECH (Ferrochelatase (FECH))
    别名
    FECH (FECH 产品)
    别名
    AI894116 antibody, Fcl antibody, fch antibody, zgc:109851 antibody, EPP antibody, FCE antibody, CG2098 antibody, Dmel\\CG2098 antibody, GB15952 antibody, ferrochelatase L homeolog antibody, ferrochelatase antibody, Ferrochelatase antibody, ferrochelatase, mitochondrial antibody, ferrochelatase HemH antibody, ferrochelatase (predicted) antibody, fech.L antibody, hemH antibody, Fech antibody, FECH antibody, fech antibody, FeCH antibody, LOC409922 antibody, hem15 antibody, APH_RS01140 antibody
    背景

    Synonyms: EPP, FCE, Ferrochelatase protoporphyria, Ferrochelatase, Ferrochelatase mitochondrial, Heme synthetase, Protoheme ferro lyase, HEMH_HUMAN.

    Background: Ferrochelatase catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway, and is localised in the mitochondrion. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. Porphyrias are a group of inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). They are broadly classified as hepatic porphyrias or erythropoietic porphyrias, based on the site of the overproduction and mainly accumulation of the porphyrins (or their chemical precursors). They manifest with either skin problems, or neurological complications, or occasionally both.

    基因ID
    2235
    途径
    Transition Metal Ion Homeostasis
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