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Occludin Protein (OCLN) (AA 266-522) (His tag)

OCLN 宿主: 大鼠 宿主: 大肠杆菌(E. Coli) Recombinant > 95 % as determined by reducing SDS-PAGE.
产品编号 ABIN7505510
发货至: 中国
  • 抗原 See all Occludin (OCLN) 蛋白
    Occludin (OCLN)
    蛋白类型
    Recombinant
    产品特性
    AA 266-522
    宿主
    • 6
    • 3
    • 1
    大鼠
    资源
    • 5
    • 2
    • 2
    • 1
    大肠杆菌(E. Coli)
    标记
    This Occludin protein is labelled with His tag.
    序列
    Lys266-Thr522
    产品特性
    A DNA sequence encoding the Rat OCLN protein (Q6P6T5) (Lys266-Thr522) was expressed with a N-His .
    纯度
    > 95 % as determined by reducing SDS-PAGE.
    Top Product
    Discover our top product OCLN 蛋白
  • 限制
    仅限研究用
  • 状态
    Lyophilized
    缓冲液
    Lyophilized from sterile PBS, pH 7.4.
    Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween80 are added as protectants before lyophilization.
    储存条件
    4 °C,-20 °C,-80 °C
    储存方法
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
    有效期
    12 months
  • 抗原
    Occludin (OCLN)
    别名
    Occludin (OCLN 产品)
    别名
    AI503564 Protein, Ocl Protein, ocln Protein, oclnb Protein, tpmt Protein, OCLN Protein, wu:fd23h10 Protein, wu:fi13c01 Protein, zgc:113992 Protein, zgc:56359 Protein, BLCPMG Protein, occludin Protein, occludin S homeolog Protein, occludin a Protein, Ocln Protein, OCLN Protein, ocln.S Protein, ocln Protein, oclna Protein
    背景

    Abbreviation: Occludin,OCLN

    Target Synonym: Occludin,OCLN_RAT,

    Background: Rat Occludin is a 523 amino acid (aa), predicted molecular weight 59 kDa integral membrane protein that localizes within tight junctions of epithelial and endothelial cells. May play a role in the formation and regulation of the tight junction (TJ) paracellular permeability barrier. May be involved in the organization of actin in endothelial cells. Defects in OCLN are the cause of band-like calcification with simplified gyration and polymicrogyria (BLCPMG), also known as pseudo-TORCH syndrome. BLCPMG is a neurologic disorder with characteristic clinical and neuroradiologic features that mimic intrauterine TORCH infection in the absence of evidence of infection. Affected individuals have congenital microcephaly, intracranial calcifications, and severe developmental delay.

    分子量

    Calculated MW: 28.16 kDa

    Observed MW: 40 kDa

    UniProt
    Q6P6T5
    途径
    Cell-Cell Junction Organization, Hepatitis C
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