Claudin 9 Protein-VLP (CLDN9)
Quick Overview for Claudin 9 Protein-VLP (CLDN9) (ABIN7488753)
Target
See all Claudin 9 (CLDN9) ProteinsProtein Type
Origin
Source
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Purpose
- Human Claudin-9 / CLDN9 Full Length Protein (VLP)
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Sequence
- Met 1 -Val 217
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Characteristics
- Human Claudin-9 Full Length Protein-VLP is expressed from human 293 cells (HEK293). It contains AA Met 1 -Val 217 (Accession # O95484-1).
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Endotoxin Level
- 1.0 EU per μg
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Claudin 9 (CLDN9) (AA 1-217) protein (His tag)
custom-made CLDN9 Origin: Mouse Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
Claudin 9 (CLDN9) (AA 1-217) protein (His tag)custom-made CLDN9 Origin: Human Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
Claudin 9 (CLDN9) proteinCLDN9 Origin: Human Host: HEK-293 Cells Synthetic Nanodisc
Claudin 9 (CLDN9) protein (Myc-DYKDDDDK Tag)CLDN9 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- PBS, Arginine, pH 7.4
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Storage
- -80 °C
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Storage Comment
- -70°C
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- Claudin 9 (CLDN9)
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Alternative Name
- Claudin-9
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Background
- Claudin-9 belongs to the claudin family. Claudins constitute integral membrane proteins responsible for solute and electrolyte permeability of the tight junction that serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets. Tight junctions also play a critical role in maintaining cell polarity and signal transductions. Claudin-9 creates charge specific channels in the paracellular space, plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity, is required to preserve sensory cells in the hearing organ because claudin-9-defective tight junctions fail to shield the basolateral side of hair cells from the K+-rich endolymph. Its ion barrier function is essential in the cochlea, but appears to be dispensable in other organs. Is one of the entry cofactors for hepatitis C virus, it enables HCV entry into target cells just as efficiently as CLDN1.
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Pathways
- Cell-Cell Junction Organization, Hepatitis C
Target
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