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Peroxisomal Biogenesis Factor 26 (PEX26) (Middle Region) Peptide

PEX26 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN5513718
发货至: 中国
  • 抗原 See all PEX26 products
    PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
    蛋白结构域
    Middle Region
    宿主
    资源
    • 6
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    AIHTARQQQK QEHSGSEEAQ KPNLEGSVSH KFLSLPMLVR QLWDSAVSHF
    产品特性
    This is a synthetic peptide designed for use in combination with anti- PEX26 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
    别名
    fk41g06 Peptide, zgc:64014 Peptide, wu:fk41g06 Peptide, PBD7A Peptide, PBD7B Peptide, PEX26M1T Peptide, Pex26pM1T Peptide, 4632428M11Rik Peptide, AI853212 Peptide, peroxisomal biogenesis factor 26 Peptide, peroxisomal biogenesis factor 26 L homeolog Peptide, pex26 Peptide, PEX26 Peptide, pex26.L Peptide, Pex26 Peptide
    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). Alternatively spliced transcript variants have been identified for this gene.

    Alias Symbols: PBD7A, PBD7B, PEX26M1T, Pex26pM1T

    Protein Size: 305
    基因ID
    55670
    NCBI登录号
    NM_001127649, NP_001121121
    UniProt
    Q7Z412
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