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PEX3 抗体

PEX3 适用: 人, 小鼠, 大鼠 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7263371
发货至: 中国
  • 抗原 See all PEX3 抗体
    PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))
    适用
    • 15
    • 9
    • 8
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 11
    • 4
    克隆类型
    • 13
    • 2
    多克隆
    标记
    • 15
    This PEX3 antibody is un-conjugated
    应用范围
    • 15
    • 9
    • 5
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human PEX3 (NP_003621.1).
    亚型
    IgG
  • 应用备注
    IHC 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
    PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))
    别名
    PEX3 (PEX3 产品)
    别名
    DDBDRAFT_0204086 antibody, DDBDRAFT_0238047 antibody, DDB_0204086 antibody, DDB_0238047 antibody, zgc:56313 antibody, PBD10A antibody, TRG18 antibody, Peroxin-3 antibody, 1700014F15Rik antibody, 2810027F19Rik antibody, 2900010N04Rik antibody, peroxisomal biogenesis factor 3 antibody, peroxin 3 antibody, peroxisomal biogenesis factor 3 L homeolog antibody, LOC692959 antibody, CpipJ_CPIJ013204 antibody, pex3 antibody, PEX3 antibody, pex3.L antibody, Pex3 antibody
    背景
    The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. 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 Zellweger syndrome (ZWS).
    基因ID
    8504
    UniProt
    P56589
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