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PEX14 抗体

PEX14 适用: 人, 小鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7263347
发货至: 中国
  • 抗原 See all PEX14 抗体
    PEX14 (Peroxisomal Biogenesis Factor 14 (PEX14))
    适用
    • 54
    • 23
    • 22
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 71
    • 3
    克隆类型
    • 72
    • 2
    多克隆
    标记
    • 30
    • 7
    • 6
    • 6
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PEX14 antibody is un-conjugated
    应用范围
    • 47
    • 39
    • 27
    • 21
    • 13
    • 13
    • 8
    • 4
    • 4
    • 3
    • 3
    • 2
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human PEX14 (NP_004556.1).
    亚型
    IgG
    Top Product
    Discover our top product PEX14 Primary Antibody
  • 应用备注
    IHC 1:50-1:200 IF 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    PEX14 (Peroxisomal Biogenesis Factor 14 (PEX14))
    别名
    PEX14 (PEX14 产品)
    别名
    ATPEX14 antibody, MQB2.13 antibody, MQB2_13 antibody, PED2 antibody, PEROXISOME DEFECTIVE 2 antibody, peroxin 14 antibody, NAPP2 antibody, PBD13A antibody, Pex14p antibody, dJ734G22.2 antibody, R75137 antibody, peroxisomal biogenesis factor 14 antibody, peroxin 14 antibody, PEX14 antibody, Pex14 antibody
    背景
    This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal. The protein also functions as a transcriptional corepressor and interacts with a histone deacetylase. A mutation in this gene results in one form of Zellweger syndrome.
    基因ID
    5195
    UniProt
    O75381
    途径
    Maintenance of Protein Location
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