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PEX1 抗体 (AA 599-628)

PEX1 适用: 人 WB 宿主: 兔 Polyclonal RB23674 unconjugated
产品编号 ABIN654140
发货至: 中国
  • 抗原 See all PEX1 抗体
    PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))
    抗原表位
    • 7
    • 7
    • 7
    • 7
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 599-628
    适用
    • 40
    • 14
    • 2
    宿主
    • 39
    • 2
    • 1
    克隆类型
    • 42
    多克隆
    标记
    • 17
    • 5
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PEX1 antibody is un-conjugated
    应用范围
    • 25
    • 23
    • 7
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This PEX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 599-628 amino acids from the Central region of human PEX1.
    克隆位点
    RB23674
    亚型
    Ig Fraction
    Top Product
    Discover our top product PEX1 Primary Antibody
  • 应用备注
    WB: 1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    储存方法
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    有效期
    6 months
  • 抗原
    PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))
    别名
    PEX1 (PEX1 产品)
    别名
    PBD1A antibody, PBD1B antibody, ZWS antibody, ZWS1 antibody, 5430414H02Rik antibody, E330005K07Rik antibody, RGD1559939 antibody, pex1 antibody, peroxisomal biogenesis factor 1 antibody, peroxisomal biogenesis factor 1 L homeolog antibody, PEX1 antibody, Pex1 antibody, pex1.L antibody
    背景
    This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome.
    分子量
    142867
    基因ID
    5189
    NCBI登录号
    NP_000457
    UniProt
    O43933
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