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OCLN (NM_002538) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC206468L1V
- LentiORF®
-
Lenti ORF particles, OCLN (Myc-DDK tagged) - Human occludin (OCLN), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 8,930.00
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规格
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Specifications
| Product Data | |
| Product Name | OCLN (NM_002538) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BLCPMG; PPP1R115; PTORCH1 |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_002538 |
| ORF Size | 1566 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC206468).
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| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_002538.2 |
| RefSeq Size | 6451 bp |
| RefSeq ORF | 1569 bp |
| Locus ID | 100506658 |
| Domains | MARVEL |
| MW | 59.1 kDa |
| Gene Summary | This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011] |
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