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PEX26 抗体 (AA 1-265)

PEX26 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1885866
发货至: 中国
  • 抗原 See all PEX26 抗体
    PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
    抗原表位
    • 5
    • 4
    • 3
    • 1
    • 1
    • 1
    AA 1-265
    适用
    • 16
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    宿主
    • 13
    • 2
    • 1
    克隆类型
    • 16
    多克隆
    标记
    • 11
    • 2
    • 1
    • 1
    • 1
    This PEX26 antibody is un-conjugated
    应用范围
    • 12
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    纯化方法
    Purified by antigen-affinity chromatography.
    免疫原
    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 265 of Human PEX26
    Top Product
    Discover our top product PEX26 Primary Antibody
  • 应用备注
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.50-1.500
    Immunofluorescence: 1.100-1.200
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    储存液
    Thimerosal (Merthiolate)
    注意事项
    Biohazard Informations: This product contains thimerosal which is hazardous.
    储存条件
    4 °C/-20 °C
    储存方法
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • 抗原
    PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
    别名
    Peroxin 26 (PEX26 产品)
    别名
    fk41g06 antibody, zgc:64014 antibody, wu:fk41g06 antibody, PBD7A antibody, PBD7B antibody, PEX26M1T antibody, Pex26pM1T antibody, 4632428M11Rik antibody, AI853212 antibody, peroxisomal biogenesis factor 26 antibody, peroxisomal biogenesis factor 26 L homeolog antibody, pex26 antibody, PEX26 antibody, pex26.L antibody, Pex26 antibody
    背景
    This gene belongs to the peroxin-26 gene family.It is probably required for protein import into peroxisomes.It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes.Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8).PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix.The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP).Two transcript variants encoding the same protein have been identified for this gene.[provided by RefSeq]
    分子量
    34 kDa
    基因ID
    55670
    NCBI登录号
    NP_060399, NM_017929
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