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PEX12 抗体

PEX12 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7258886
发货至: 中国
  • 抗原 See all PEX12 抗体
    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
    适用
    • 30
    • 11
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 26
    • 3
    • 1
    克隆类型
    • 28
    • 2
    多克隆
    标记
    • 12
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PEX12 antibody is un-conjugated
    应用范围
    • 20
    • 18
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human PEX12 (NP_000277.1).
    亚型
    IgG
    Top Product
    Discover our top product PEX12 Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    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
    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
    别名
    PEX12 (PEX12 产品)
    别名
    zgc:56182 antibody, pex12 antibody, MGC81372 antibody, PEX12 antibody, DDBDRAFT_0186545 antibody, DDBDRAFT_0238076 antibody, DDB_0186545 antibody, DDB_0238076 antibody, LOC100226224 antibody, PAF-3 antibody, PBD3A antibody, Peroxin-12 antibody, AI451906 antibody, peroxisomal biogenesis factor 12 antibody, peroxisomal biogenesis factor 12 L homeolog antibody, RING zinc finger-containing protein antibody, pex12 antibody, PEX12 antibody, pex12.L antibody, Pex12 antibody
    背景
    This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS).
    分子量

    Observed_MW: 41 kDa

    Calculated_MW: 40 kDa

    基因ID
    5193
    UniProt
    O00623
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