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

OCLN Origin: Rat Host: Escherichia coli (E. coli) Recombinant > 95 % as determined by reducing SDS-PAGE.
Catalog No. ABIN7505510
  • Target See all Occludin (OCLN) Proteins
    Occludin (OCLN)
    Protein Type
    Recombinant
    Protein Characteristics
    AA 266-522
    Origin
    • 6
    • 3
    • 1
    Rat
    Source
    • 5
    • 2
    • 2
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This Occludin protein is labelled with His tag.
    Sequence
    Lys266-Thr522
    Characteristics
    A DNA sequence encoding the Rat OCLN protein (Q6P6T5) (Lys266-Thr522) was expressed with a N-His .
    Purity
    > 95 % as determined by reducing SDS-PAGE.
    Top Product
    Discover our top product OCLN Protein
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    Lyophilized from sterile PBS, pH 7.4.
    Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween80 are added as protectants before lyophilization.
    Storage
    4 °C,-20 °C,-80 °C
    Storage Comment
    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.
    Expiry Date
    12 months
  • Target
    Occludin (OCLN)
    Alternative Name
    Occludin (OCLN Products)
    Synonyms
    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
    Background

    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.

    Molecular Weight

    Calculated MW: 28.16 kDa

    Observed MW: 40 kDa

    UniProt
    Q6P6T5
    Pathways
    Cell-Cell Junction Organization, Hepatitis C
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